How to Make an Immune System and a Foreign Host Quickly Cohabit in Peace? The Challenge of Acute Graft-Versus-Host Disease Prevention After Allogeneic Hematopoietic Cell Transplantation.

Allogeneic hematopoietic cell transplantation (alloHCT) has been used as cellular immunotherapy against hematological cancers for more than six decades. Its therapeutic efficacy relies on the cytoreductive effects of the conditioning regimen but also on potent graft-versus-tumor (GVT) reactions mediated by donor-derived immune cells. However, beneficial GVT effects may be counterbalanced by acute GVHD (aGVHD), a systemic syndrome in which donor immune cells attack healthy tissues of the recipient, resulting in severe inflammatory lesions mainly of the skin, gut, and liver. Despite standard prophylaxis regimens, aGVHD still occurs in approximately 20-50% of alloHCT recipients and remains a leading cause of transplant-related mortality. Over the past two decades, advances in the understanding its pathophysiology have helped to redefine aGVHD reactions and clinical presentations as well as developing novel strategies to optimize its prevention. In this review, we provide a brief overview of current knowledge on aGVHD immunopathology and discuss current approaches and novel strategies being developed and evaluated in clinical trials for aGVHD prevention. Optimal prophylaxis of aGVHD would prevent the development of clinically significant aGVHD, while preserving sufficient immune responsiveness to maintain beneficial GVT effects and immune defenses against pathogens.

Introduction

For almost 6 decades, allogeneic hematopoietic cell transplantation (alloHCT) has been the cornerstone of poor risk hematological cancer therapy. Although novel sophisticated cellular therapies (such as those with CAR T cells) have emerged and appear to be occupying a growing place in the modern therapeutic arsenal in hematology, their long-term effects on disease control and survival are still unclear. Therefore, alloHCT still remains standard of care in a variety of high risk hematological disorders, often offering the only curative option for these diseases (1). The persisting major role of alloHCT in current medicine is documented by the constant increase in the annual number of stem cell transplants performed worldwide, with >19,000 alloHCT procedures in Europe and associated countries in 2018 (701 centers in 50 countries) (2). In adults, the most frequent indications for alloHCT remain acute leukemia (more than 50% of all alloHCT), followed by myelodysplastic syndromes and non-Hodgkin lymphoma (2). In addition, an acceptable donor can currently be found for almost all patients, mainly due to the recent development of innovative platforms for alloHCT with HLA-haploidentical family donors (mismatched for one of the two HLA haplotypes).

The therapeutic efficacy of alloHCT against hematological cancers relies on the cytoreductive effects of the conditioning regimen but also (and mainly) on potent graft-versus-tumor (GVT) reactions, defined as immune-mediated reactions by donor cells against tumor cells. However, beneficial GVT effects may be counterbalanced by acute GVHD (aGVHD), a systemic syndrome in which donor immune cells attack healthy tissues of the recipient, resulting in severe inflammatory lesions mainly of the skin, gut and liver. Despite more than 6 decades of preclinical and clinical researches, the immunological requirements necessary to achieve GVT effects without promoting aGVHD have not been fully established.

Despite standard prophylaxis regimens, aGVHD occurs in approximately 20–50% of transplanted patients and is a major cause of treatment failure and mortality after alloHCT. Therefore, the prevention of aGVHD after alloHCT represents an unmet medical need in the modern era of cancer immunotherapy and research must continue in this field. Here, we provide a brief overview of criteria for aGVHD diagnosis and grading as well as current knowledge on aGVHD immunopathology. Then, we discuss current approaches and novel strategies being developed and evaluated in clinical trials for aGVHD prevention.

What is aGVHD? The Clinical Point of View

GVHD is separated into two syndromes, historically defined according to the time frame of occurrence of symptoms: acute GVHD (aGVHD) occurring within the first 100 days after transplantation and chronic GVHD (cGVHD) developing thereafter. Although simple, this classification based only on empirical observations and did not rely on actual biological or clinical bases. More recent classification systems have emphasized differentiating a- and cGVHD based on pathophysiological mechanisms and clinical manifestations (3, 4).

In 2018, a consortium of GVHD experts from the European Society for Blood and Marrow Transplantation (EBMT), the National Institutes of Health (NIH) and the Center for International Blood and Marrow Transplant Research (CIBMTR) reviewed the terminology and guidelines for GVHD diagnosis and scoring (5). Clinically, aGVHD typically presents with inflammatory lesions, the three main organs involved being: the skin (erythematous and pruriginous maculopapular skin rash), the gastro-intestinal (GI) tract (nausea, vomiting, and anorexia with weight loss in the upper tract; and/or watery or bloody diarrhea, crampy abdominal pain and/or ileus in the lower tract), and the liver (cholestasis with hyperbilirubinemia) (5, 6). Typical aGVHD is defined by the presence of these exclusive inflammatory manifestations, without any other sign consistent with cGVHD. Ideally, the diagnosis of aGVHD should be confirmed by positive histological findings, but this is not formally required (5). AGVHD can be categorized as “classic aGVHD” in the setting of typical aGVHD manifestations occurring less than 100 days after alloHCT or donor lymphocyte infusion (DLI), and “late, recurrent or persistent aGVHD” in patients with typical aGVHD signs experienced later than 100 days after alloHCT/DLI (5, 7).

Grading aGVHD is essential because it is predictive of non-relapse mortality and it guides therapeutic management. Several scoring systems have been developed during the past decades, including the original Glucksberg classification (first established in the 1970s), the “Modified Glucksberg” or “Keystone”, the IBMTR and the “MAGIC” scoring systems (8–11). Each of them proposes a 4-grade scale, integrating the individual stage of each target organ (skin, GI tract, and liver), with or without the general Performance Status. Recently, the EBMT−NIH−CIBMTR Task Force Consortium recommended the MAGIC criteria as the most accurate and detailed clinical criteria for diagnosis and grading the severity of aGVHD (5). A web-application has also been developed based on this position statement (eGvHDApp; ) and has been found to be helpful in improving aGVHD and cGVHD scoring consistency and compliance with guidelines (12, 13).

In addition to the typical manifestations of aGVHD in the skin, GI, and liver, there is accumulated evidence that aGVHD may also affect other tissues, including the cellular niches in the bone marrow (BM), thymus and secondary lymphoid organs (14). Although lesions in these organs are hardly clinically detectable, they can severely impact outcome by impairing hematopoiesis, compromising T- and B-cell reconstitution and predisposing to the development of subsequent cGVHD (15). It has also been suggested that aGVHD can cause damages to the endovascular endothelium and can be the trigger of endothelitis-related complications after alloHCT, such as transplant-associated microangiopathy, diffuse alveolar hemorrhage, idiopathic pneumonia syndrome (16). Finally, over the past decade, experimental data (17, 18) and clinical case reports (19) have gradually accumulated suggesting that the central nervous system may also be a potential target of aGVHD. Although they are not considered in current standard aGVHD diagnosis criteria and grading systems, alloreactive lesions to these tissues can be associated with significant morbidity.

Despite conventional prophylactic measures, it is estimated that 20–50% of transplanted patients develop clinically significant grades II–IV aGVHD after alloHCT. Known risk factors include the stem cell source (G-SCF mobilized peripheral blood stem cells, PBSC), the donor type (unrelated, female donor for a male recipient), the degree of donor/recipient HLA-mismatch, the intensity of the conditioning regimen (myeloablative regimen), the occurrence of severe infections during the peri-transplant period and administration of DLI (7, 20, 21).

The standard first-line of treatment for grades II–IV aGVHD is high-dose systemic corticosteroids. However, aGVHD fails to respond to steroids in approximately 30–50% of patients (the risk increasing with increasing grade), therefore requiring subsequent lines of immunosuppressive therapies (22, 23). Outcomes of patients with steroid refractory aGVHD have been dismal (up to 60–85% of non-relapse mortality at 2 years), partly due to aGVHD by itself, but also to cumulative toxicity and increasing susceptibility to infections and relapse incurred with additional immunosuppressive therapy (22, 24). Hopefully, research is constantly developing in the field and two recent large phase III studies have provided significant benefit in efficacy outcomes with two novel strategies for the treatment of steroid refractory aGVHD. First, Socie et al. reported better long-term overall survival with inolimomab (an anti-CD25 monoclonal antibody) in comparison with anti-T cell globulin (25). The second phase III study demonstrated higher response rate with ruxolitinib (a JAK 1–2 inhibitor) compared to the investigator's therapy of choice (26). Nevertheless, aGVHD remains a severe complication and one of the major cause of early post-transplant mortality (27).

What is aGVHD? The Immunological Point of View

Despite significant improvements in the field over the past 20 years, the complex immunobiology of aGVHD still remains only partially elucidated. Here, we present a simplified overview of the main basic immunological concepts on aGVHD biology, with the aim of providing readers with some clues for understanding the rationale of both current and emerging preventive approaches. For more detailed information about aGVHD pathophysiology, readers are referred to several outstanding reviews (6, 28–30).

Donor T Cells as Drivers, Amplificators, and Effectors of aGVHD Responses

AGVHD after alloHCT mainly results from donor T-cell alloreactivity against the recipient's tissues, as evidenced by the low incidence of GVHD observed in patients transplanted with a T-cell depleted allograft (31). After alloHCT, transferred donor T cells are able to recognize structurally dissimilar allogeneic peptide/HLA complexes in the recipient, reacting against either polymorphic HLA molecules (in case of alloHCT with HLA-mismatched donor/recipient pair) and/or peptides (minor histocompatibility antigens) presented by either shared or dissimilar HLA molecules (in the setting of alloHCT with HLA-matched or mismatched donor/recipient pair, respectively) (32–34).

In general, three types of signals are required to generate full alloreactive T-cell responses after alloHCT ( ) (6, 28–30, 35). The first triggering event that makes a donor T cell alloreactive is the activation of its TCR by the peptide/HLA complex (signal 1). TCR engagement leads in the activation of a series of intracellular downstream signaling pathways that ultimately result in the nuclear translocation of key transcription factors such as nuclear factor-kappa B (NF-κB), Adaptor-related Protein complex 1 (AP1), and nuclear factor of activated T cell (NFAT), whose coordinated activity orchestrates the complete activation of the T cell, its proliferation and its synthesis of cytokines and cytokine receptors, such as IL-2 and CD25 (the α subunit of the high affinity αβγ forms the IL-2 receptor) (36). Besides the basic biology, the blockade of one of these TCR-downstream signaling pathways, namely the NFAT calcium/calcineurin-dependent transduction pathway, was one of the first strategies explored to repress alloreactive T-cell activation after alloHCT in pioneered preclinical and clinical studies (37) and is still currently universally used as a standard approach for aGVHD prophylaxis (see below). Inhibition of the NF-κB pathway was also demonstrated to be efficacious for reducing proliferation, survival, cytotoxic functions and production of cytokines in alloreactive T cells during aGVHD (38–40).

Figure 1

Signals 1, 2, 3 of T-cell activation and sites of action of several molecules used or tested in clinical trials for aGVHD prevention. Sites of action of current approaches (blues circles) and developing strategies (orange circles) are presented. Beyond their effects on Teff, several of these molecules have also effects on other cell types (see text). [adapted from (35)].

Along with TCR activation, additional positive costimulation (signal 2) is required to allow complete T-cell activation and avoid anergy or apoptosis (41). Multiple T-cell positive costimulatory molecules have been identified to play role in aGVHD, such as CD28, inducible co-stimulator (ICOS), OX40, and 4-1BB [nicely reviewed in (41, 42)] ( ). Their cognate ligands [namely B7 ligands (CD86 or CD80), B7-related protein-1 (B7RP-1), OX40L and 4-1BBL, respectively] are highly expressed at the surface of mature antigen presenting cells (APCs). Among all of the T-cell costimulatory receptors, the most extensively studied is CD28, which is constitutively expressed at the surface of naive T cells. Another B7 receptor, induced with T-cell activation, is cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) that has similar structure to CD28 and acts as a competitor for CD80 and CD86 ligation, resulting in dowregulation of T-cell responses. Blockade of CD28/B7 interactions has been shown to attenuate alloreactive T-cell activation, induce tolerance to host alloantigens and to reduce aGVHD in in vitro studies and animal models of alloHCT (43–46). One of these approaches consists in using fusion proteins of the Fc region of human immunoglobulin with the extracellular domain of CTLA4 (CTLA4-Ig) (43, 45) and is tested for aGVHD prevention in clinical trials (see below).

The third signal for sustained T-cell activation, acquisition of effector functions and survival is provided by cytokines [signal 3, nicely reviewed in the context of aGVHD in (42, 47)]. Among all, IL-2 is a key cytokine for alloreactive T-cell proliferation and survival. Produced by activated T cells, IL-2 acts through paracrine and autocrine signaling, further providing a self-activation loop. Among others, IL-2 receptor intracellular signaling in T cells include JAK (janus kinase)/STAT (signal transducers and activators of transcription) pathways (namely JAK1 and JAK3/STAT5 in particular) ( ) (48, 49). JAK1/2 pathways are also involved in signal transduction downstream the receptors of multiple other cytokines (such as IL-6, IL-12, ...) and play major role in T-cell proliferation, polarization, and metabolic reprogramming (49). Pharmacological inhibition of JAK1/2 pathways was demonstrated to reduce aGVHD in preclinical models (50) and to be efficacious for the treatment of patients with steroid refractory-aGVHD (see above, INTRODUCTION) (26). Mechanisms of JAK1/2 inhibition on aGVHD reactions include at least decreased Th1 and Th17 differentiation, but also broad anti-inflammatory and immunosuppressive effects on multiple immune cell types [reviewed in (50)]. It is commonly accepted that pathogenic Th1 and Th17 cells as well as their polarizing cytokines [IL-12 and interferon gamma (IFNγ); IL-6, IL-1β, IL-21 and IL-23, respectively] play important role during aGVHD (42, 47, 51). Among all cytokines, IL-6 is the hallmark of pro-inflammatory cytokines and increased systemic IL-6 levels were reported in patients early after alloHCT (52, 53). IL-6 signaling in donor T cells is critical for the polarization of donor naive T cells towards Th17/Tc17, but IL-6 also exerts many other effects (such as several on DC and regulatory cells) (54, 55).

Mechanistic/mammalian target of rapamycin (mTOR) is another key signaling kinase in T cells that integrate an array of activating signals (including the three aforementioned signals of T-cell activation) and environmental cues to regulate cell survival, growth, proliferation, differentiation, and metabolism (56). Inhibition of mTOR Complex 1 (mTORC1) has demonstrated efficacy against aGVHD in preclinical models (56–58) and has been explored as GVHD prevention in clinical trials for several years (see below).

Over the past decade, it has become increasingly clear that metabolic reprogramming of the T cell is required to enable the transition from a naive T cell to a proliferative and differentiated T cell that will drive immune effector functions and mediate aGVHD. Studies have reported that effector T cells use multiple metabolic pathways (glycolysis, oxidative phosphorylation, fatty acid oxidation, glutaminolysis) to keep the pace with high energy demands during aGVHD, (59, 60). Furthermore, the metabolic demand of different T cell subsets is likely not identical.

A key event in the initiation phase of aGVHD is the interaction of CD4+ and CD8+ donor T cells with activated APCs (via cross-presentation for the latter) that provide the three aforementioned signals. During the initiation phase of aGVHD, most of the APCs are host-derived hematopoietic APCs and host non-hematopoietic APCs (intestinal epithelial cells, keratinocytes, myofibroblasts...) (61, 62). By expressing pattern recognition receptors (PRR) such as Toll-like (TLR) and nucleotide oligomerization domain (NOD)-like receptors, innate immune cells and some epithelial cells are able to detect danger signals such as sterile DAMP (damage-associated molecular pattern molecules, which are released from dying cells or disrupted extracellular matrix) and PAMP (pathogen-associated molecular pattern molecules, which can be released from invasive bacteria, fungi or viruses at the epithelial surfaces). After alloHCT, an increased number of DAMP and PAMP molecules can be released as a consequence of cytotoxic conditioning regimen or aGVHD [reviewed in (63)]. After alloHCT, several studies have demonstrated that host exposure to gut microbial flora and PAMPs due to disrupted intestinal barrier can be an important initiating event in aGVHD reactions (64–67). Mechanisms include the recruitment and activation of host neutrophils (which further contribute to tissue damage and inflammation) as well as inflammatory macrophages, dendritic cells and non hematopietic APCs (which further prime T cells) (61, 67–69).

Beyond T-cell activation and clonal expansion, T-cell chemotaxis towards secondary lymphoid organs and target tissues are also important in aGVHD immunobiology [nicely reviewed in (70)]. For example, among the so-called "homing receptors", the chemokine-receptor CCR7 and the L-selectin (CD62L) are expressed at the surface of naive and central memory T cells and direct them to secondary lymphoid organs in which they can be primed and activated by professional APCs. This raises the hypothesis that T cells may contribute differently to aGVHD according to their differentiation status, with naive CD4+ T cells being more prone to cause aGVHD than (late) effector memory CD4+ T cells (71, 72). In addition, T-cell migration towards GVHD target organs is also crucial to cause aGVHD. Namely, the chemokine receptor CCR5 is involved in T-cell migration towards lymph nodes, the GI tract and the liver. Hence, CCR5-chemotaxis blockade was reported to limit aGVHD in some murine models (73, 74). Integrins also participate in T-cell migration to target organs and the specific tissue expression of some of them may make their study interesting in the context of aGVHD. Several mouse studies have indeed suggested that α4β7 integrin on donor T cells was important for T-cell migration into gut-associated lymphoid tissues and for the development of GI aGVHD (75, 76).

After being primed by APCs in secondary lymphoid organs, activated and differentiated donor T cells migrate to target organs where they generate effector T cell (Teff) responses (effector phase of aGVHD). Cytotoxic T cells can cause direct target tissue cell death via diverse cytolytic pathways that involve the release of granzyme B and perforin and the expression of members of the tumor necrosis factor (TNF) family (including FasL). Immune activation and tissue lesions lead to a cytokine storm that further recruits multiple cellular effectors (e.g. other T cells, neutrophils, and activated macrophages) and brings molecular effectors (e.g. TNF-α, IFN-γ, complement molecules, reactive oxygen species, ...), further intensifying tissue lesions and inflammatory responses (amplification phase) and thus leading to sustained aGVHD reactions and severe end-organ damages.

Mechanisms Establishing Immune Cell and Tissue Tolerance During aGVHD

As mentioned above, Teff cell activation and proliferation are negatively regulated by co-inhibitory signals. In addition to these T-cell intrinsic pathways, peripheral immune tolerance can also be achieved by the intervention of several anti-inflammatory molecules as well as tolerogenic cells. In the context of aGVHD, all of these components can help restraining the destructive machinery of immune cell and limiting tissue damages.

Numerous investigations have focused on regulatory T cells (Tregs), which can exert multiple tolerogenic and anti-inflammatory effects [nicely reviewed in (77–79)]. Tregs are characterized by the expression of the master forkhead box protein 3 transcription factor (FoxP3) and their constitutive expression of the surface receptor CD25, the high affinity IL-2R α-chain (in contrast to Teff in which CD25 expression starts upon the TCR activation) (80). Hence, in steady-state conditions (low dose of IL-2), Tregs capture all the IL-2 molecules in the milieu, therefore quenching spurious activation of Teff. There are several types of CD4+ Treg: (1) "natural thymus-derived T (nTreg or tTreg), generated from lymphoid precursors in the thymus; and (2) "peripheral Treg" (pTreg), derived from the differentiation of conventional naive T cells in secondary lymphoid organs in the context of low-dose or tolerogenic antigen exposure and upon IL-10 and TGF-β stimulation. pTreg can also be generated in vitro and in this case are referred as “induced T” (iTreg). Interestingly, preclinical studies in mice have shown that co-transplanting high doses of CD4+ iTreg or infusing fewer freshly isolated Treg from donor peripheral blood (likely containing a mixture of t- and pTreg) several days prior to alloHCT in lymphopenic conditions was effective for mitigating allogeneic and human xenogeneic GVHD (81, 82). However, one issue with Treg adoptive transfer could be their phenotypic and functional instability in the context of prolonged inflammation (such as during aGVHD), causing them to lose their immunosuppressive properties and even acquire pro- inflammatory functions. Such observations were made in mice (83, 84) but also with human Treg in the context of xenogeneic GVHD (85).In comparison to tTreg, the expression of FoxP3 is more unstable in iTreg, since they lack the locked-in gene expression signature of transcription factors implicated in FoxP3 activity stabilization. Specifically, hypermethylation of FoxP3 gene/promoter in iTreg was reported to destabilize their phenotype (86). By contrast, phenotypic and functional stabilization of Treg cells has been demonstrated with hypomethylating agents in a model of xenogeneic GVHD (87).

Type 1 regulatory T cells (Tr1) are another subset of suppressive peripheral T cells, still suppressing immune response similarly to t- and pTreg but characteristically lacking CD25 and Foxp3 lineage marker expression (88). Although if this subpopulation has been only partly unraveled so far, Tr1-like cells are being considered more and more important for immune response homeostasis. Similarly to iTreg, Tr1-like cells can be induced in vitro (88, 89), and a recent preclinical co-transfer study has shown promising results for suppressing GVHD (89).

Other cell types that have been reported to exert immunoregulatory properties during aGVHD, include invariant natural killer T cells (iNKT), natural killer cells (NK), innate lymphoid cells (ILC), tolerogenic dendritic cells, various myeloid suppressor populations of hematopoietic [e.g., myeloid-derived suppressor cells {MDSCs}, CD34+ regulatory monocytes] and stromal origin [e.g., mesenchymal stromal cells (MSCs)] (90–92). In particular, iNKT cells are under increased investigation, owing to their reported suppressive activity against GVHD in preclinical models (93, 94).

In addition to these tolerogenic immune cell subtypes, other non-immune cells and components of the damaged organs can also reveal protective properties in the context of aggression, through several mechanisms including the up-regulation of anti-inflammatory surface receptors, release of tolerogenic soluble factors and activation of repairing mechanisms (a concept known as “tissue-tolerance”). This concept has been described in recent nice articles (95, 96). Among others, IL-22, keratinocyte growth factor (KGF), R-spondin-1 (R-Spo1) and glucagon-like peptide 2 (GLP-2) were reported to be protective against GI manifestations of aGVHD (e.g. by preserving and/or enhancing the regeneration of intestinal epithelial cells, intestinal stem cells and/or Paneth cells) (97–101). Paneth cell secretion of antimicrobial peptides (e.g. α-defensin) is also critical for maintaining the GI microbial ecosystem (97).

There is also growing evidence that the commensal microbiota at mucosal and cutaneous surfaces plays important role in tissue homeostasis and immune tolerance after alloHCT. This concept has been particularly studied at the intestinal interface [nicely reviewed in (102)]. It was recently reported that the bacterial and viral gut microbiota is altered (with loss of diversity and dominance of some taxa) after alloHCT and that such dysbiosis may be associated with aGVHD outcomes (103–107). Regarding bacteria, low intestinal abundance of gut commensals belonging to the Lactobacillales, Clostridiales and Blautia genus was reported to be associated with and increased incidence of lethal aGVHD and poor survival (104, 108). Consistent with this, increased risk of aGVHD-related death was also reported with the use of some anti-anaerobic or broad-spectrum antibiotics in mice and in patients (104, 109–111). However, most of the aforementioned studies were based on associations, and the causations as well as the precise mechanisms of how the microbiota can influence immune and tissue tolerance post-allo-HCT remain to be determined. Recent data suggested that an important way could be through microbiota-derived metabolites (112, 113). A recent elegant work has indeed highlighted significant variations in microbiota-derived metabolites (especially aryl hydrocarbon receptor ligands, bile acids and plasmalogens) at the onset of aGVHD in patients (114). A significant reduction in fecal levels of butyrate [a short-chain fatty acid (SCFA) generated by the fermentation of non-digestible carbohydrates by certain anaerobic commensal bacteria] in patients after alloHCT was also alloHCT reported by another group (114). Interestingly, in a mouse model, restoring butyrate levels, either by direct administration of butyrate or by changing the composition of intestinal microbiota towards an increase in butyrogenic bacteria (e.g. selected strains of Clostridia) mitigated aGVHD and improved survival (115). Understanding the precise effects of all these metabolites on host tissues and immunity is the subject of intense current research, with some data already suggesting various potential roles in enhancing the trophicity and regenerative properties of the intestinal epithelium as well as in modulating innate and adaptive immune responses (102, 112, 113). Overall, these findings highlight the likely major role of the microbiome-metabolome axis in aGVHD, which may offer potential new targeted strategies to explore for improving aGVHD prophylaxis or treatment.

How to Prevent aGVHD After alloHCT? When the Clinician Meets the Immunologist

Conventional Strategies for aGVHD Prevention

Currently, there is no standardized aGVHD preventive approach. However, the backbone of most conventional prophylactic regimens is based on T-cell immunosuppression, by the pharmacological inhibition of their clonal expansion and activation and/or by their direct depletion (116). Here, we provide a short overview of the current standard regimens for aGVHD prevention and briefly describe their biological rationale. For detailed clinical considerations, readers are referred to the recently published 2019 EBMT consensus recommendations for aGVHD prophylaxis and treatment (117).

Since the mid-1980s (37), the most commonly adopted GVHD prophylaxis regimens among patients given alloHCT with BM or PBSC from HLA-matched sibling or unrelated donor consist in the combination of an anti-metabolite [either short course of methotrexate (MTX) or mycophenolate mofetil (MMF)] with a calcineurin inhibitor [CNI, either cyclosporin A (CSA) or tacrolimus (FK506, tacro)]. The former (MTX or MMF) delete proliferating T cells, while the second (CNI) blocks TCR-induced T-cell activation (signal 1) by interfering with NFAT nuclear translocation thereby reducing transcription of IL-2 ( ).

Several other alternative regimens have also been explored with the aim of improving the control of aGVHD and/or reducing drug toxicity. Among them, administration of mTOR inhibitors [of which sirolimus (siro) is the most widely studied molecule] has been tested for several years ( ). Unlike CNIs which, by reducing IL-2 production, limit Teff activation but with a concomitant negative impact on IL-2-dependent Treg, inhibition of the mTOR signaling pathway precludes the activation of Teff while preserving Treg activity (which are less dependent on the mTOR/Akt pathway) (58, 118). Several randomized phase III trials have addressed the effects of siro either as a substitution of MTX (tacro + siro vs. tacro + MTX) in myeloablative TBI-based alloHCT (119) or in addition to the standard prophylaxis (tacro + MMF + siro triplet regimen) after non-myeloablative/RIC-alloHCT (120). Although these studies provided encouraging results, clinical data and experience with siro are still considered insufficient to recommend its routine use as part of the prophylactic regimen (117). Moreover, a warning has been issued with the use of siro after high dose busulfan-based conditioning regimens due to the increased risk of sinusoidal obstruction syndrome (121).

For almost two decades, in vivo T-cell depletion using serotherapies with rabbit anti-T-cell globulin (ATG, ATG-Thymoglobulin® or ATG-Grafalon®) (122–126) or alemtuzumab (ALEM, an anti-CD52 monoclonal IgG1 antibody) (127) has also been used to prevent GVHD. Both of these antibody preparations have a long half-life in the human plasma and therefore, once administered as part of the conditioning regimen, they exert their biological effects for several weeks after the graft infusion and induce profound depletion of both host and donor immune cells (128, 129). Moreover, besides the pan T-cell depletion ( ), ATG and ALEM also mediated a variety of other immune effects [detailed in other informative reviews (130, 131)]. Several large randomized phase 3 trials have demonstrated the benefit on both a- and cGVHD incidence of adding ATG to standard prophylaxis in the setting of MAC-alloHCT with PBSC (122–126). In a related approach, ex-vivo immune cell depletion of the graft (e.g. by immunomagnetic positive selection of CD34+ stem cells or ALEM in the bag) was also evaluated and proved to be effective to prevent GVHD (132–134). However, a major concern with such an approach is its negative impact on GVL effects and immune recovery.

In recent years, there has been an exponential increase in the number of haplo-alloHCT performed worldwide. This was made possible thanks to the development of innovative platforms for GVHD prevention in this peculiar high alloreactivity setting. Among them, the advent of post-transplant cyclophosphamide (PTCy) has revolutionized this procedure and can be considered as one of the major advances in the field of alloHCT over the past two decades (135–139). This approach, designed by the John Hopkins University group in Baltimore, consists in the administration of (one or) two boluses of high dose cyclophosphamide (Cy, a nitrogen mustard alkylating agent) shortly after alloHCT (day +3 and/or +4) followed by MMF/tacro prophylaxis (starting from day +5). The initial rationale of this strategy mostly assumed to be a cytotoxic and selective depletion of highly proliferative Teff (supposed to be the newly primed alloreactive T cell clones during the first days after the graft infusion) ( ), while preserving resting hematopoietic stem cells and non-alloreactive T cells (such as anti-infectious memory T cells) (135). Additional researches further demonstrated that PTCy also induces central tolerance by additional intrathymic clonal deletion of alloreactive T cell precursors (140, 141). Moreover, it was recently suggested that beyond these effects on Teff, PTCy-mediated protection against GVHD also (and mainly) relies on the promotion of Treg and the induction of tolerance (135, 141). Treg are indeed less sensitive than Teff to the Cy cytotoxic effects due to their higher expression of aldehyde dehydrogenase (the major detoxifying enzyme for cyclophosphamide) (142). In murine PTCy haplo-alloHCT models, Kanakry et al. showed that PTCy does not completely eliminate alloreactive Teff, but instead alters T-cell response to alloantigens and induces the rapid and preferential recovery and expansion of Treg (142). Evidence for the pivotal role of Treg in PTCy-mediated immune tolerance is also illustrated by the development of severe and fatal GVHD when FoxP3+ Treg are depleted (143). Going back to clinical studies, the pioneer pilot trial with the PTCy strategy led by the Baltimore group reported a very low incidence of grade III–IV aGVHD (10%) in patients transplanted with HLA-haploidentical BM after non-myeloablative conditioning regimen (138). Similar encouraging results were further observed by numerous other groups, even using PBSC as the stem cell source and more intensive conditioning regimens (139, 144). Beyond haplo-alloHCT, PTCy recently starts gaining popularity in other settings, including HLA-matched sibling/unrelated donor and HLA-mismatched unrelated donor alloHCT (145). Recently, in a large multicenter phase III trial comparing several novel immunosuppressive prophylactic regimens (PTCy + tacro +MMF; tacro + MMF + bortezomib; tacro + MMF + maraviroc) with the contemporary standard tacro + MTX scheme after RIC-alloHCT, PTCy + tacro + MMF appeared to be the most promising intervention, yielding the best GvHD-free, relapse-free survival (GRFS) (146). It is currently unknown whether another combination (i.e. MMF/siro) can be as effective as MMF/CNI in addition to PTCy in haplo-alloHCT, or even if PTCy can be safely used as a single agent after HLA-identical sibling transplantation. It is the subject of numerous investigations.

Developing Strategies for aGVHD Prevention

The deeper understanding of aGVHD immunobiology has facilitated the diversification of preventive strategies, and many novel approaches are currently under investigation (6, 29, 116). The concrete clinical goal of aGVHD prophylaxis after alloHCT is to prevent or at least to significantly reduce the damage to target tissues induced by alloreactive immune responses in order to decrease the risk of clinically relevant organ dysfunction leading to “clinical aGVHD”. To achieve this objective, the current strategies being developed/under investigation for limiting aGVHD after alloHCT can be categorized according to three main areas of intervention: (1) limitation of donor-derived immune cell alloreactivity, (2) promotion of immune tolerance, and (3) modulation of the target tissue environment to make it less prone to but rather more resistant to aGVHD immunopathology and to improve regenerative properties. Given the large number of strategies under development, it is difficult to cover them all. Here, we have chosen to present some of those which have already reached clinical trials and which seem to be the most promising in our opinion ( ).

Table 1

Developing strategies for aGVHD prevention.

		Teff depletion	Inhibition of signal 1 of Teff activation	Inhibition of signal 2 of Teff activation	Inhibition of signal 3 of Teff activation	Inhibition of Teff trafficking	Promotion of immune tolerance	Modulation of microenvironment
Developing strategies	Ongoing clinical trial	Main putative mechanisms of action
Ex vivo depletion of TCRαβ+/CD19+ donor cells[phase I–II (147)]	NCT04088760 (phase II)NCT02508038 (phase I)	X
Ex vivo depletion of CD45RA+ naive T cells[phase II (148)]		X
Ex vivo photodepletion of anti-host reactive donor T cells (Kiadis) [phase II (149)]	NCT02999854 (phase III)	X					X
Proteasome inhibitors (bortezomib)[phase I–II (146, 150, 151)]	NCT03945591 (phase II)NCT03082677 (phase II)NCT01991301 (phase I)NCT02145403 (phase I–II)		X			X	X	X
α-CTLA-4 Ig (abatacept, belatacept)[phase II (152–156)]	NCT02867800 (phase I)NCT01743131 (phase II)NCT04380740 (phase II)			X
Anti-IL-6 receptor antibody (tocilizumab)[phase I–II (52, 53)]	NCT03434730 (phase II)				X			X
Janus kinases inhibitors(anti-JAK1/2 ruxolitinib, and baricitinib; anti-JAK1 itacitinib)	NCT02806375 (phase I–II)NCT04131738 (phase I)NCT04127721 (phase II)NCT03755414 (phase I)NCT03320642 (phase I)				X		X	X
Demethylating agents (5-azacytidine, decitabine)[phase I–II (157)]	NCT00813124 (phase II)NCT01758367 (phase I–II)	X	X	X	X	X	X	X
Histone deacetylase inhibitors (vorinostat, panobinostat)[phase I–II (158, 159)]	NCT03842696 (phase I–II)NCT03842696 (phase I–II)NCT02588339 (phase II)	X	X	X	X	X	X	X
CCR5 blocker (maraviroc)[phase I–II (74, 146, 160)]	NCT02799888 (phase II)					X
α4β7 integrin blocker(vedolizumab)(phase I–II) (161)	NCT03657160 (phase III)					X
Low dose IL-2[phase I (162, 163)]	NCT02659657 (phase II)						X
Treg infusion[phase I–II (reviewed in (164)]	NCT01795573 (phase I)NCT03977103 (phase II)NCT04013685 (phase I)						X
Mesenchymal stromal cells[phase I–II (reviewed in (165))]	NCT02270307 (phase II–III)NCT01045382 (phase II)NCT04247945 (phase II–III)						X
iNKT cells[αgalCer, phase II (166) , TLI conditioning (129)]	NCT03605953NCT00631072						X
Recombinant urate-oxidase[phase I (167)]	–							X
Alpha-1-antitrypsin	NCT03805789 (phase II-III)							X
Keratinocyte growth factor [phase I-II (168, 169)]	–							X
Probiotics and fecal material transplantation[phase I-III (170–172)]	NCT03720392 (phase II)							X
Prebiotics	NCT02805075 (phase I)NCT02763033 (phase II)							X

Strategies Aimed at Limiting Alloreactivity of Donor Immune Cells (Mainly T Cells) Against Host Tissues (red); Strategies Aimed at Promoting Immune Tolerance (blue); Strategies Aimed at Modulating Target Tissue Environment (green).

Strategies Aimed at Limiting Alloreactivity of Donor Immune Cells (Mainly T Cells) Against Host Tissues

As donor Teff are main causative agents of aGVHD, huge efforts have been made to optimize and refine donor Teff depleting approaches, e.g. by selectively depleting specific T-cell subpopulations. In particular, the selective depletion of TCRαβ+ cells, of naive T cells, or even of activated alloreactive T cells (e.g. with ex vivo photodepletion of anti-host reactive donor T cells) has demonstrated encouraging results for aGVHD prevention (147–149). Besides Teff depleting approaches, strategies aimed at functionally interfering with Teff activation (signal 1, 2 and/or 3, ), intracellular signaling pathways, metabolism and homing properties are also developing as well as gene editing approaches.

As described above, signal transduction downstream of TCR activation (signal 1) in Teff occurs through multiple pathways that result in the nuclear translocation of key transcription factors, including NFAT, NF-κB and AP1. Blockade of the NFAT calcium-dependent transduction pathway with CNI (CSA or tacro) is universally used as standard GVHD prophylaxis. Inhibition of the NF-κB pathway also recently appeared as an interesting approach. Proteasome inhibitors, such as bortezomib (BOR), have been shown to suppress NF-κB activation (in part by reducing the degradation of its inhibitory protein IκBα) and were reported to confer protection against GVHD in mouse models (39). Moreover, by reducing the degradation of many other intracellular proteins, blocking the proteasome also has an impact on T-cell chemotaxis, secretion of inflammatory cytokines, APC functions and promote Treg (173). Based on these observations, the early addition of short-course BOR (on days +1, +4, and +7 after alloHCT) to standard tacro/MTX has been assessed in phase I–II clinical trials and provided encouraging results (150). However, in a large open-label three-arm phase 2 randomized trial comparing conventional Tacro/MTX vs. BOR/Tacro/MTX and vs. BOR/Tacro/Siro after UD RIC-alloHCT, BOR-based regimens failed to show an improvement in day +180 aGVHD incidence (32.6, 31.1 and 21%, respectively) (151). Similarly, in another large prospective phase II study comparing several novel prophylactic regimens with contemporary MTX/tacro controls, the addition of BOR to standard MTX/tacro in RIC-alloHCT did not result in lower aGVHD incidence (146). Combination of BOR with other agents, such as PTCy, as well as use of other proteasome inhibitors (carfilzomib, ixazomib) is currently under investigation ( ).

Targeting costimulatory signals at the APC/T-cell interface (signal 2) has also been investigated as aGVHD prophylaxis for several years. Of all these strategies, the one that has reached the more advanced stage of development concerns CTLA4-Ig (abatacept, belatacept). Addition of abatacept to background CNI-based aGVHD prophylaxis in the setting of alloHCT with HLA-matched donor has produced promising results in phase I–II clinical trials (152, 153). Addition of abatacept to the PTCy platform is also under investigation in the setting of haplo-alloHCT for non-malignant disorders (154, 155). Moreover, unlike T-cell anergy, recent data have shown that NK cell cytotoxicity is not altered, but even enhanced in the presence of CTLA4-Ig. This makes the CTLA4-Ig approach an interesting strategy for reinforcing GVT effects while still limiting aGVHD risks in the setting of HLA-mismatched donor (haplo) transplantation. This hypothesis prompted several groups to study the CTLA4Ig sequential primed donor lymphocyte (DLI) infusion protocols after PTCy-based haplo-alloHCT as adoptive immunotherapy in patients with advanced malignant disorders (156). Of note, one issue with targeting CD80/CD86 with CTLA4-Ig may be associated with concurrent undesired blockade of tolerogenic CTLA4-dependent signaling to Treg and APCs. Hence, CD28-specific inhibition is under investigation in preclinical studies (44).

Different strategies that target signal 3 of T-cell activation by blocking cytokines or their receptors were also tested in clinical studies (42, 47). Among them, blockade of IL-2 signaling with monoclonal antibodies binding to the IL-2 receptor α-chain CD25 (e.g. basiliximab, daclizumab, inolimomab) was unfortunately discouraged for controlling aGVHD since it was reported to be associated with increased GVHD-related mortality (174, 175). This is likely due to the negative impact of IL-2 blockade on suppressive Treg since IL-2 is not only crucial for Teff expansion but also for Treg homeostasis.

IL-6, TNF-α, and IL-1β are important pro-inflammatory cytokines in aGVHD pathogenesis. Addition of Tocilizumab (an anti-IL-6 receptor monoclonal antibody) to CNI/MTX prophylaxis has been tested in phase I–II studies and has been shown to be associated with a very low incidence of grades II–IV aGVHD (<15%) (52, 53). However, these promising results have to be confirmed in larger phase III studies. By contrast, inhibition of TNF-α or IL-1β added to standard GVHD prophylaxis failed to prevent aGVHD (176, 177). Several additional cytokines (such as IL-12, IL-23, GM-CSF, etc.) have also been implicated in aGVHD pathogenesis, and their inhibition should also be evaluated in the future.

T cells respond to many inflammatory cytokines (including IL-6) through JAK/STAT pathways. As described above, several studies have shown that the inhibition of JAK1/2 pathways (i.e. with ruxolitinib and baricitinib, two JAK1/2 inhibitors, or with itacitinib, a selective JAK1 inhibitor) prevented aGVHD in preclinical model (50) and was efficacious for controlling steroid refractory-aGVHD in patients (26). Further ongoing studies are investigating the use of this molecule and other JAK1/JAK2 inhibitors for aGVHD prevention ( ). Itacitinib, which inhibits JAK1 while sparing JAK2, is expected to have reduced myelosuppressive activity compared to broader specificity JAK inhibitors.

Encouraging results also come from epigenetic modifiers [e.g. demethylating agents such as 5-azacytidine, decitabine, histone deacetylase inhibitors (HDACi)] which can exert pleiotropic effects on aGVHD reactions, not only on the fate of Teff but also on other immune cells (such as Treg and DCs) (157–159). For example, the addition of vorinostat (a HDACi) to standard GVHD prophylaxis after alloHCT with HLA-matched donors was examined in two phase 2 clinical trials (158, 159). Both studies showed that vorinostat was well tolerated and was associated with a low incidence of aGVHD (grade II-IV aGVHD less than 25%, and grades III–IV less than 10%). Additional advantages of such approaches lie in the fact that, besides their immunomodulatory effects, these molecules (demethylating agents and HDACi) can also exert anti-tumor activity, therefore offering opportunities for mitigating GVHD while enhancing anti-tumor effects.

Interfering with the homing of Teff towards target organs can be viewed as an additional strategy for preventing aGVHD. A phase I–II study indeed investigated the addition of maraviroc (a CCR5 antagonist) to standard tacro/MTX after RIC-alloHCT in adults and demonstrated a low incidence of visceral (GI and liver) grades II–IV aGVHD (14.7%) (74). Similar encouraging results were observed in pediatric patients (160). Nevertheless, a recent multicenter phase II trial comparing several new prophylactic regimens with contemporary MTX/tacro controls in RIC-alloHCT showed that, when added to standard MTX/tacro, maraviroc did not result in lower GVHD rates compared to PTCy or BOR (146). The redundant mechanisms in the signaling of chemokines/chemokine receptors may be an explanation for the limited effectiveness of strategies based on blocking just a single chemokine receptor. Integrins also represent attractive potential targets for novel preventive therapies against GVHD. Low incidences of grades II–IV overall and lower-intestinal aGVHD (19 and 14% at day 100, respectively) were recently observed in a phase Ib study in which patients received vedolizumab (an antibody directed againts α4β7 integrin) in combination with standard tacro/MTX (161). A large phase III randomized placebo control trial evaluating vedolizumab added to standard aGvHD prophylaxis is currently recruiting (NCT03657160, ).

Finally, since T cells consume a lot of energy during aGVHD, it can also be envisaged that targeting metabolic pathways and subverting the use of T-cell energy could offer other potential innovative preventive strategies to explore in the future. The challenge will be to make these molecules specific enough to avoid important toxicities.

Strategies Aimed at Promoting Immune Tolerance

Rather than trying to decrease the reactivity of the donor immune cells, another way of preventing aGVHD after alloHCT may be through the promotion of tolerance between the donor immune cells and the recipient, by strengthening the tolerogenic arm of the immune system. Indeed, cell-based approaches to promote immune tolerance have shown encouraging results. In our view, the most promising are Treg, iNKT, and MSC-based therapies.

Early clinical trials with iTreg infusion in patients have shown promising results for aGVHD prevention (178–180), [reviewed in (164)]. Nevertheless, the major problem with the clinical transfer of Treg is the difficulty of reaching a sufficient number of Treg with good purity to infuse and of ensuring that the transferred cells persist and retain their tolerogenic properties in the inflammatory context of aGVHD (181). Strategies aimed at promoting Treg proliferation in the donor before Treg donation, for example by pretreating the donor with TNF superfamily receptors DR3 agonists, have been reported to be effective in murine models (182) but have not yet been explored in humans. The scientific community is currently focusing on examining approaches to promote in vivo Treg expansion and stability within the recipient. In particular, the high sensitivity of Treg to IL-2 (determined by their constitutive expression of CD25) makes treatment with low doses of this cytokine an interesting approach. A phase I–II study investigated the administration of ultra-low dose IL-2 (100,000–200,000 IU/m2, 3 times/week) after alloHCT and reported promising results in terms of safety and low incidence of aGVHD (0/16 patients experienced grade II–IV aGVHD) (162). Another study using a similar approach is underway in China (NCT02659657, ). However, in another trial administration of low doses of IL-2 in addition to tacro/siro for GVHD prophylaxis failed to prevent aGVHD despite resulting in higher Treg levels (163).

As with iTreg, adoptive transfer of IL-10/TGF-β producing Tr1 cells is gradually being seen as a new option for the prevention of aGVHD. A pilot phase 1 clinical trial evaluating the safety of Tr1 cell co-transplantation in pediatric patients in an HLA-mismatched donors setting is currently being planned (NCT03198234).

A high content of iNKT cells in the transplant has been reported to be associated with a reduced risk of aGVHD in clinical studies (183). Thus, protocols for promoting the expansion of iNKT cells (e.g. through ex or in vivo manipulations) appear as attractive novel strategies to explore in order to prevent aGVHD. Clinical studies involving the ex vivo expansion of iNKT cell populations are underway (NCT00631072, NCT03605953, ). Recently, it was reported that RGI-2001, a CD1-binding synthetic derivative of alpha-galactosylceramide, activates and expands iNKT cells in vivo (166). Conditioning regimens that foster the induction of iNKT cells, such as total lymphoid irradiation, are also being considered (129).

MSCs are multipotent progenitor cells that reside within the BM microenvironnement and several other connective tissues such as the adipose tissue, the umbilical cord, and placenta membranes. Among a wide variety of functions, MSCs also have a multiplicity of immunomodulatory and anti-inflammatory properties, making them attractive candidates to consider as cell-based therapies to prevent aGVHD. Moreover, MSCs are hypoimmunogenic and can therefore be derived from third-party HLA-mismatched donors. A number of preclinical studies using various animal models have evaluated the effectiveness of MSCs in alleviating GVHD. However, results were mixed, with some studies reporting benefits (184), while others did not (185). Several factors, including MSC tissue of origin (BM, adipose tissue, cord blood, placental membranes), cell dose, timing of infusion and pre-activated MSC status likely influenced the results and caused heterogeneity between studies. Pilot clinical studies have also suggested a potential role for MSCs in preventing GVHD (186–188), [reviewed in (165)]. Further studies are currently underway to more precisely assess the impact of MSC co-transplantation on aGVHD ( ).

Strategies Aimed at Modulating Target Tissue Environment

Beyond targeting Teff and promoting immune tolerance, approaches aimed at controlling target tissue environment to make it less pro-inflammatory and/or aimed at strengthening its mechanisms of resilience, repair and regeneration (“tissue tolerance”) may be considered as complementary strategies to be exploited to mitigate aGVHD clinical severity.

Among others, molecules aimed at reducing danger signal production (e.g. recombinant urate-oxidase, alpha-1-antitrypsin) are currently under investigation (167, 189, 190).

Tissue-protective/regenerative approaches that promote the healing of aGVHD-related tissue damages have also emerged as promising complementary strategies to standard aGVHD immuno-prophylaxis. As mentioned above, KGF, R-Spo1, IL-22, and GLP-2 were reported to be protective during GI aGVHD (97–101). To the best of our knowledge, among all these molecules, only KGF has been tested to date in clinical trials for aGVHD prevention. Two phase 1/2 randomized, double-blind, placebo-controlled studies tested peri-transplant palifermin (KGF) administration in combination with standard prophylaxis (168, 169). Both of them failed to demonstrate benefit in terms of reduction of severe grades III–IV aGVHD. Clinical trials on IL-22 IgG2-Fc (NCT02406651) and GLP-2 (Teduglutide, NCT04290429) for the treatment of GI aGVHD are underway, and it is plausible that these drugs will soon be tested for aGVHD prophylaxis.

The accumulation of evidence on the involvement of the commensal microbiota in intestinal tissue homeostasis and immune tolerance post-alloHCT has also recently opened up the concept of manipulating the gut microbiota as an innovative approach to prevent aGVHD. Several strategies under study include careful risk-balanced use of broad-spectrum antibiotics, dietary or pharmaceutical interventions to limit growth of noxious bacterial taxa [i.e. eviction of lactose (191) or enteral immunoglobulin administration (192)] and direct transfer of living microbial species using fecal material transplantation (FMT) (170, 171) or selective transfer of microbial consortia (probiotics) (172, 193, 194). Some of them have already reached clinical trials (see ). As such, FMT appears to be a promising approach to improve microbiota diversity in alloHCT patients and to limit aGVHD (170, 171). However, considering the highly immunocompromised status of alloHCT patients, safety of FMT should be carefully established in this specific population, particularly regarding risk of bacterial translocation, septicemia and norovirus infection (195, 196). The modulation of the microbiome–metabolome axis with prebiotic/postbiotic interventions is also under investigation. Among others, the microbiota-derived SCFA butyrate appears as an important metabolite for intestinal homeostasis and immune tolerance after alloHCT. Interestingly, one approach for stimulating microbial SCFA production could be via dietary supplementation with non-digestible carbohydrates that can be metabolized by selected commensal gut bacteria. Such strategy is currently being explored in clinical trials in alloHCT patients ( ). Among them, a phase II clinical trial is testing the safety and early efficacy for GVHD prevention of an oral dietary supplement containing potato-based starch [which was reported to increase microbial butyrate production in healthy volunteers (197)] (NTC02763033). Besides SCFAs, roles of other microbial metabolites (such as indole derivatives, peptides derived from bile acids, aryl hydrocarbon receptor ligands, polyamine, plasmalogens) would also be interesting to explore in the future.

Conclusion and Perspective

AGVHD is a severe complication after allogeneic stem cell transplantation. It results from a highly deregulated immune process, involving a complex network of multiple molecular and cellular mediators and effectors causing end-organ damages mainly to the skin, GI tract and/or liver. Despite prophylactic measures, aGVHD still develops in about 20–50% of transplanted patients, making it an unmet medical need in alloHCT survivorship research. Improved understanding of the pathology of aGVHD has led to the development of novel strategies to optimize its prevention, with some of them appearing particularly promising based on early data from clinical trials. However, these and other new strategies that will be developed in the future will have to be tested in prospective phase 3 trials before they can become standard. Standardization of aGVHD definition criteria and severity grading system using the validated MAGIC criteria will be vitally important to guarantee the quality, reproducibility and interpretation of these future clinical studies.

Theoretically, it would be logical to think that the combination of multiple approaches targeting several aGVHD immunopathological pathways would ultimately provide a complete suppression of aGVHD. However, the complete abrogation of donor-derived immunity after alloHCT is clinically irrelevant, as this would seriously compromise the engraftment, anti-infectious immune reconstitution as well as the beneficial GVT effects. The ideal step in the future would rather be to provide a personalized risk-stratified aGVHD prophylaxis regimen for each patient, reserving intensive immunosuppressive regimens for patients at high risk for aGVHD and avoiding excessive immunosuppression for those at a low risk for aGVHD. To make this approach feasible, the development of future algorithms to improve the accuracy of aGVHD risk prediction will be an essential prerequisite. Algorithms may be based on HLA disparities and other factors, including predictive biomarkers, clinical predictive factors and genetic variants associated with increased risk of aGVHD. Recipient and/or donor single nucleotide polymorphisms (SNPs) for chemokines, cytokines, costimulatory molecules, and micro-RNAs (miRNAs) would also likely allow transplant physicians to identify specific immune profiles predictors of aGVHD in the future. However, these analyses are not yet accessible for a routine assessment in daily clinical practice.

Unlike immunosuppressive strategies, approaches aimed at modulating the interactions between the host and gut microbiota and/or promoting the regenerative properties of the target tissue of aGVHD would likely not increase the risk of non-engraftment or relapse after alloHCT and would therefore appear to be interesting complementary approaches to combine with classical GVHD immunosuppressive prophylaxis. At present, little is known about the precise mechanisms of host–microbiota cross-talk and about tissue-specific tolerance to diseases, but it is a topic of growing interest and intense research.

Author Contributions

BV and LC are co-first authors. TK and SS are co-last authors. All authors contributed to the article and approved the submitted version.

Funding

The review was supported by funds from the FBC (ref 2017-037), the FNRS (ref 7.4607.19), King Baudouin Foundation (ref J1813410), the Anti-Cancer Center and the Leon Fredericq Foundation from the University of Liege. and were adapted and republished from the Belgian Journal of Hematology (Belg J Hematol 2020;11(4):159–173) (35).

Conflict of Interest

HS has received travel grants and/or speaker honoraria from Incyte, Janssen, Jazz Pharmaceuticals, Novartis, Takeda, Celgene and Abbvie. She also received research funding from Novartis for an investigator-initiated study. FB has received travel grants and/or speaker honoraria from Celgene, AbbVie, Novartis, Pfizer and Sanofi. CG has received travel grants and/or speaker honoraria from Amgen, Incyte, Janssen, Astellas, Novartis, Celgene. TK has received travel grants and/or speaker honoraria (never on personal account) from Celgene, BMS, Roche, Merck, Novartis, Pfizer and Sanofi. SS has received travel grants and/or speaker honoraria from Novartis, Fresenuis-Kabi, Gilead, Sanofi, Jazz Pharmaceuticals, Merck, BMS and Celgene. She also received a grant from Gilead for a basic research project.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.