Graft Versus Host Disease After Intestinal Transplantation: A Single-center Experience.

BACKGROUND: Graft versus host disease (GVHD) is an uncommon but highly morbid complication of intestinal transplantation (ITx). In this study, we reviewed our 17-y experience with GVHD focusing on factors predicting GVHD occurrence and survival.
METHODS: Retrospective review of 271 patients who received 1 or more ITx since program inception in 2003 with survival analysis using Cox proportional hazard modeling.
RESULTS: Of 271 patients, 28 developed GHVD 34 (18-66) d after ITx presenting with rash or rash with fever in 26, rectosigmoid disease in 1, and hemolysis in 1; other sites, mainly rectosigmoid colon, were involved in 13. Initial skin biopsy demonstrated classic findings in 6, compatible findings in 14, and no abnormalities in 2. Additional sites of GVHD later emerged in 14. Of the 28 patients, 16 died largely from sepsis, the only independent hazard for death (hazard ratio [HR], 37.4181; P = 0.0008). Significant (P < 0.0500) independent hazards for occurrence of GVHD in adults were pre-ITx functional intestinal failure (IF) (HR, 15.2448) and non-IF diagnosis (HR, 20.9952) and early post-ITx sirolimus therapy (HR, 0.0956); independent hazards in children were non-IF diagnosis (HR, 4.3990), retransplantation (HR, 4.6401), donor:recipient age ratio (HR, 7.3190), and graft colon omission (HR, 0.1886). Variant transplant operation was not an independent GVHD hazard.
CONCLUSIONS: Initial diagnosis of GVHD after ITx remains largely clinical, supported but not often confirmed by skin biopsy. Although GVHD risk is mainly recipient-driven, changes in donor selection and immunosuppression practice may reduce incidence and improve survival.

INTRODUCTION

Graft versus host disease (GVHD) is an uncommon complication of solid organ transplantation (SOT) with an incidence ranging between <1% and 10%[1-4] that contrasts with the 40%–50% incidence after hematopoietic stem cell transplantation (HSCT).[5-7] Incidence of GVHD after intestinal transplantation (ITx) lies at the upper end of the SOT range, attributed to a large number of alloreactive T cells within an intestinal graft. Consequently, interest in GVHD after ITx remains high, especially in the context of mortality that ranges between 40% and 77%.[2,8-12]

Recent descriptions of GVHD after ITx by several centers have demonstrated a typical presentation with rash mainly appearing 2 wk to 2 mo postoperatively but occasionally delayed for no apparent reason.[2,3,8-13] Diagnosis is largely clinical, as routine rash histopathology commonly fails unambiguously to distinguish GVHD from drug reaction or viral infection.[8,14,15] Techniques to confirm suspicion of donor T cells in a tissue are not routinely available, and magnitude of peripheral blood T-cell chimerism in ITx recipients with and without clinical evidence of GVHD overlaps.[10,16] Response to intensified immunosuppressive drug therapy is often poor, implying that donor alloreactive cells are relatively resistant to standard immunosuppression compared with recipient alloreactive cells. Both inefficacy and toxicity of established treatments contribute to the relatively high mortality.

Recently, we have demonstrated that donor-derived clones in native colon mucosa of selected ITx recipients with typical features of GVHD have a CD69+ resident memory T-cell phenotype.[17] Complimentary to this work, we herein report our clinical GVHD experience after ITx with a heightened focus on risks for occurrence compared with ITx recipients not developing GVHD.

MATERIALS AND METHODS

Charts of all patients who underwent ITx at this center from inception of the program in 2003 until June 30, 2019, were reviewed.

Indications for ITx and Variant Operations

Isolated ITx (IITx) was performed for irreversible intestinal failure (IF) with early but progressing intestinal failure–associated liver disease (IFALD), progressive central vein loss, and nonmetastasizing neoplasms compromising the midgut.[18] En bloc liver-intestine-pancreas transplant was performed for advanced IFALD with portal hypertension primarily in pediatric patients,[19] whereas noncomposite liver and intestinal transplantation (LITx) was performed for the same indication in adults.[20] Multivisceral transplant (MVTx) including stomach, small intestine, liver, and pancreas plus splenectomy was performed for advanced IFALD with both unsalvageable foregut and midgut and for extensive portal–mesenteric vein thrombosis.[20] Modified multivisceral transplant (MMVTx) that excludes a liver graft was performed for similar indications as IITx but with unsalvageable foregut.

Clinical Transplant Practice

Practices maintained throughout the study period are summarized in Table 1, whereas changes over time potentially relevant to GVHD and other immunological events are summarized in Table 2.[18,21,22] Rabbit antithymocyte globulin (r-ATG) was administered to donors during organ procurement except when not logistically feasible or precluded by hemodynamic instability. Early post-ITx exposure to either sirolimus (SIR) or mycophenolate mofetil was defined as a minimum of 14 d of treatment either immediately before onset of GVHD or, for those not developing GVHD, within the first month after ITx including postoperative d 30.

TABLE 1.

ITx management practices throughout the study period 2003–2020

Induction immunosuppression
	Methylprednisolone, 50 mg/kg (maximum 1600 mg) during first post-ITx week tapered daily
	Then, prednisolone/prednisone 1 mg/kg (maximum 20 mg) daily tapered to 0.1 mg/kg (maximum 5 mg) daily by 6 mo after ITx
Maintenance immunosuppression
	Prednisone/prednisolone 0.1 mg/kg (maximum 5 mg) daily indefinitely
	Tacrolimus
		Target trough level 25 ng/mL during first post-ITx month
		Target trough level 7–12 ng/mL by eighth post-ITx month, low-end if secondary immunosuppression and high-end if no secondary immunosuppression
Secondary immunosuppression options
	Sirolimus
		Target trough level 3–5 ng/mL
		Preferred for superior bioavailability
		Discontinued if frequent infections
		Replaced with MMF if renal, pulmonary, or mucosal toxicity
	MMF
		Target trough level 2–4 μg/mL
		Preferred if established renal insufficiency
		Discontinued if frequent infections
		Replaced or discontinued if hypersensitivity including mucosal ulceration
Nutrition
	Elemental—semielemental diet, starting 1 wk post-ITx and continued 6–12 mo post-ITx
	Dietary fat restriction for 1 mo post-ITx
	Oral intake starting 2–4 wk post-ITx
	Liquid diet by tube if feeding disorder
	Taper parenteral nutrition to maintain age- and size-appropriate body weight
Graft stoma construction
	Ileostomy
		Preferred
		Closure 3–5 mo post-ITx if no interval rejection
	End colostomy
		If pre-ITx colectomy
		Endorectal pull-through individualized

ITx, intestinal transplant; MMF, mycophenolate mofetil.

TABLE 2.

Modifications in ITx practices during the study period 2003–2020

Year
2008
	Pre-ITx recipient screening for preformed anti-HLA antibodies by single-antigen assay.
	Virtual cross-matching for identification of preformed, donor-specific anti-HLA antibodies.
	Substitution of induction immune suppression using basiliximab (postoperative d 0 and 4, 10–20 mg/dose), formerly for all ITx recipients, with rabbit antithymocyte globulin for sensitized ITx recipients defined by panel reactive anti-HLA antibody level >20% or positive crossmatch (postoperative d 0–4, 1.5 mg/kg/d).
2009
	Standardized inclusion of graft ileocecal valve and graft ascending/transverse colon.
	Loop in preference to Santulli ileostomy.
2012
	High-dose intravenous immunoglobulin, rituximab (anti-CD20 monoclonal antibody), and plasmapheresis immediately before and after ITx in HLA antibody-sensitized recipients.
	Monitoring for donor-specific anti-HLA antibodies arising de novo after ITx and treatment with intravenous immunoglobulin when present.

ITx, intestinal transplant.

Graft Monitoring

Protocol surveillance endoscopy and biopsy of the graft via ileostomy or colostomy commenced 1 wk after transplant reduced gradually over time to once yearly panendoscopy after stoma closure. Native colon was inconsistently assessed during protocol surveillance but routinely after suspicion of GVHD elsewhere. Biopsy findings were classified as graft rejection, infection, posttransplant lymphoproliferative disorder, GVHD, and miscellaneous pathologies based on standard criteria.[23,24] Humoral rejection was not routinely evaluated.

Evaluation and Treatment of GVHD

Appearance of a symmetrical, erythematous maculopapular rash most typically on the hands and feet, hairline, chest, and abdomen corresponding to acute disease[8,25] prompted a skin biopsy evaluated by a dermatopathologist. Skin biopsies were classified as (1) GVHD-classic, (2) GVHD-consistent, or (3) normal based on pathology reports; GVHD grade in classic disease was recorded when specified. Features required for diagnosis of classic GVHD included vacuolar interface degeneration, full-thickness keratinocyte necrosis, or satellite cell necrosis,[14,26-28] whereas less specific but GVHD-compatible features included spongiosis, eosinophilia, less extensive keratinocyte necrosis, and perivascular and perieccrine inflammation.[29] Skin biopsies, endoscopy, and other investigations were repeated as necessary to evaluate disease progression and flare. GVHD therapy was not protocolized and varied with individual practitioners and as new therapies became available.

Peripheral blood chimerism was determined if GVHD was suspected clinically and typically rechecked with persistent or worsening disease. Methodology was based on polymorphisms in short tandem repeats with lower limit of detection at 1%. For most of the study, assays detected total peripheral blood chimerism and since 2017, CD3 (T cell)-specific chimerism. Intermediate-resolution HLA typing was obtained by rSSO-XR assay (One Lambda, West Hills, CA) using genomic DNA. A degree of HLA matching was determined using serologic equivalents and HLA class I cross-reactive groups (Tables S1 and S2, SDC, http://links.lww.com/TXD/A344).[30,31]

Analysis

To facilitate most analyses, pre-ITx diagnoses were classified into 3 groups: (1) anatomic IF, that is, short bowel syndrome; (2) functional IF subdivided into intestinal pseudoobstruction (“dysmotility”) including total to near-total aganglionosis and intractable diarrhea associated with congenital mucosal disease; and (3) non-IF, consisting of intraabdominal and pelvic tumors, most commonly desmoids associated with familial adenomatous polyposis, and portal–mesenteric thrombosis generally due either to a primary hypercoagulable disorder or secondary to advanced liver disease including complications of previous isolated liver transplantation. Chemotherapy for tumors before ITx could not be determined in most cases. Underlying genetic disorders were either confirmed by diagnostic testing or presumed on the basis of typical clinical features. Patients aged ≥18 were classified as adult and those <18 y as pediatric.

Comparisons of continuous variables were made using the Wilcoxon and Mann-Whitney tests, and proportions were compared using the Fisher and Fisher-Freeman-Halton tests; central tendencies were expressed as medians with interquartile range (first quartile–third quartile). Cox proportional hazards regression was used in outcome modeling as indicated; June 30, 2020, was the censor date. Significance was taken as P < 0.0500. Statistical calculations were performed using MedCalc Statistical Software (Ostend, Belgium). This retrospective review was conducted under the authorization of the Institutional Review Board of Georgetown University (ID #2004-008).

RESULTS

Clinical Presentation of GVHD

Twenty-eight patients (14 adults, 16 male individuals), median age at ITx = 16.0 (1.7–41.8) y, were diagnosed with GVHD from among the 271 patients receiving 278 ITx through June 30, 2019, giving a GVHD incidence of 10%. Underlying diseases leading to ITx were anatomic IF in 6, functional IF in 11 (dysmotility in 6 and mucosal disease in 5), and non-IF in 11 (abdominal tumor in 6, primary or secondary portal–mesenteric thrombosis in 5). Incidence of GVHD did not differ between secretory diarrhea and dysmotility within the functional IF group (P = 0.1484) or between tumor and thrombosis diagnoses within the non-IF group (P = 1.0000). Known or presumed genetic diagnoses in 13 of the 28 patients included familial adenomatous polyposis in 4, microvillus inclusion disease in 2, and 1 each of multiple intestinal atresia with severe combined immunodeficiency syndrome, Kabuki syndrome, megacystis microcolon intestinal hypoperistalsis syndrome, total intestinal aganglionosis, trichohepatoenteric syndrome, tufting enteropathy, and prothrombin gene mutation. Types of ITx performed included IITx in 10, LITx in 5, MVTx in 11, and MMVTx in 2.

First symptoms and signs of GVHD appeared 34 (18–66) d after ITx in 2 clusters, an early period with a median interval after ITx of 30 (17–55) d in 25 patients and a late period in the remaining 3, median interval after ITx being 353 (309–381) d (early versus late, P = 0.0053). Irrespective of time of onset, all cases had an acute phenotype. Figure 1 summarizes evolving patterns and distributions of disease activity. The first indication of GVHD was a rash in 24 of the 28 patients. Fever (median 38.8 [38.1–40.1] °C) appeared within 24 h of rash in 14 of the 24 patients and preceded the rash by 96 h in 2 additional patients. As indicated in Figure 1, of the 26 patients whose presentation of GVHD was as a rash or fever soon followed by rash, contemporaneous evaluation revealed active disease at other sites in 13, the most common being native rectosigmoid colon. Of these 26 patients, 22 had a skin biopsy available for review that was obtained 6 (2–14) d after onset of rash or fever. Disease was classified as GVHD-classic in 6 patients (grade II in 4, grade I in 1, and unspecified in 1), GVHD-compatible in 14 patients, and normal in 2. In patients with GVHD-compatible biopsies, the most common alternative histopathological diagnosis was drug reaction that was discarded or rejected because of worsening of rash despite medication change or detection of GVHD elsewhere.

FIGURE 1.

Sequence of organ involvement in GVHD after intestinal transplantation in 28 patients. *Clinical—not proven by biopsy in 1. ^Direct antiglobulin negative but remission under steroids and rabbit antithymocyte globulin in 1. #Clinical—not proven by biopsy. ^^Delayed until 96 h after fever in both patients. **Incidental finding. GVHD, graft vs host disease.

Absolute lymphopenia was common at diagnosis in the 25 patients with early onset GVHD, typically more severe after r-ATG compared with basiliximab induction (median 600 [400-760] per μL versus 900 [670-1300] per μL, P = 0.0466). In contrast, simultaneous median absolute neutrophil count was 7600 (2730–11 700) per μL and did not vary with induction method (P = 0.4663). Total peripheral blood chimerism determined 4 (0–10) d after first symptoms or signs in 19 of the 28 patients demonstrated a median donor percentage of 0% (0–2.8), the 2 highest values equaling 25% and 50%. Peripheral blood CD3 cell chimerism at GVHD onset in 3 of the most recently transplanted patients with multisite disease equaled 6.0% (4.5–13.8), which equivocally exceeded simultaneous total peripheral blood chimerism of 0.0% (0.0–1.3) in these 3 (P = 0.0625).

Treatment and Late Disease Activity

Treatment of GVHD was as outlined in Figure 2. Initial therapy included corticosteroids, mostly intravenous, except for 1 patient whose immunosuppression was curtailed in an unsuccessful attempt to stimulate rejection of donor alloreactive cells. Additional agents, mostly r-ATG, supplemented corticosteroids at diagnosis mainly based on severity of clinical presentation and in 1 patient, 50% donor total peripheral blood chimerism referred to above. Mycophenolate mofetil or SIR was maintained in 21 patients, in 19 for 98 (38–174) d after GVHD diagnosis, similarly distributed between patients receiving corticosteroids alone or in combination with other therapies.

FIGURE 2.

Sequential treatment of graft vs host disease after intestinal transplantation in 28 patients. E-ATG, antithymocyte globulin (equine); ECP, extracorporeal photopheresis. GVHD, graft vs host disease; IV, intravenous; r-ATG, antithymocyte globulin (rabbit).

Responses to treatment included sustained complete GVHD remission, a transient complete response followed by relapse at the initial or new site(s), or partial or no response. Partial and nonresponders received additional therapy that included more corticosteroids plus other treatments shown in Figure 2. Cutaneous disease commonly recurred or worsened as initially normal or GVHD-compatible skin biopsies progressed to GVHD grade I in 1 patient, grade II in 6 patients, grade III in 2 patients, and grade IV in 1 patient. Furthermore, 14 patients demonstrated new sites of disease at a median of 73 (36–190) d after GVHD onset including skin disease in 2 patients initially without this finding. GVHD remained purely cutaneous in 5 of the 28; features of this mild phenotype group are summarized in Table 3.

TABLE 3.

Patients with cutaneous GVHD alone

Patienta	Skin biopsy	Fever at presentation	Initial chimerismb (%)	Treatment	GVHD recovery
1	Initial: classicc grade II	Yes	0	• Topical tacrolimus and steroids• Methylprednisolone IVd	Yes
2	Initial: compatibleeLater: classic grade II	No	2	• Topical steroids• ECP	Yes
3	Initial: compatible	Yes	0	• Methylprednisolone IV	Yes
4	Initial: compatible	Yes	0	• Topical tacrolimus• Methylprednisolone IV and rabbit antithymocyte globulin	Yes
5	No biopsy	No	0	• Topical steroids	Yes

In chronological order of transplant date.

Total peripheral blood.

Classic GVHD histopathology defined as vacuolar interface degeneration, full-thickness keratinocyte necrosis, or satellite cell necrosis.

Methylprednisolone started before chimerism testing.

GVHD-compatible features included spongiosis, eosinophilia, less extensive keratinocyte necrosis, and perivascular and perieccrine inflammation.

ECP, extracorporeal photopheresis; GVHD, graft vs host disease; IV, intravenous.

Outcome of GVHD

Of the 28 patients with GVHD, 12 (43%) were alive on June 30, 2020, 3.0 (2.1–4.8) y after ITx. Of the 16 patients who died, GVHD was ongoing in 10 at death 10.4 (7.6–11.6) mo after disease onset, while the remaining 6 patients died after GVHD remission 27.9 (8.6–35.0) mo after disease onset (P = 0.0824). Of those dying with active GVHD, sepsis was the primary cause of death or important contributor to death in all 9 patients in whom details about death were known. The most common fatal pathogen was aspergillus (5 patients); others included cytomegalovirus, toxoplasma, and Enterobacter cloacae. The 6 deaths among the 18 patients who had recovered from GVHD resulted from infections that included adenovirus, Candida glabrata, and aspergillus. In total, 8 patients experienced aspergillus infection, of whom 3 had received intermittent prophylaxis with micafungin (death in 2). All 7 patients who developed an Epstein-Barr virus-driven posttransplant lymphoproliferative disorder recovered with treatment. Grade I (mild) graft rejection occurred in 1 patient 17 d before recognition of GVHD that resolved despite relapsing skin and lung involvement. Grade III (severe) rejection developed 15.0 (4.5–23.2) mo after onset of GVHD in 6 patients of whom 5 had experienced GVHD recovery. The sole patient with ongoing GVHD had persistent ulcerative rectosigmoid colon disease when rejection was identified in graft ileum and colon 3 wk before death.

Characteristics of the 12 patients surviving and 16 patients dying after GVHD are summarized in Table 4. As shown in Table 4, nonsurvivors demonstrated greater peripheral blood chimerism, clinical indications of more severe and refractory disease including emergence of new sites of involvement, and more numerous and severe complications. Reflecting employment for worsening and refractory disease, no individual therapy was associated with favorable outcome. Univariable Cox modeling (Table 5) also indicated an increased hazard for death with an underlying genetic disease, equivocal death hazard from splenectomy-inclusive ITx, and reduced death hazard with IITx. Nevertheless, the multivariable Cox model also shown in Table 5 demonstrated that only sepsis was independently associated with fatal GVHD outcome. There was no association between survival and initial skin biopsy findings (GVHD-classic versus compatible, P = 0.9351, and normal versus GVHD-compatible, P = 0.2679).

TABLE 4.

Factors associated with survival and death after GVHD in 28 patients following intestinal transplantation

Explanatory variable			P a
Pretransplant recipient factors
Primary disease type	Short bowel syndrome—survived	50.0%, n = 3/6	0.8948
	Functional intestinal failure—survivedb	36.4%, n = 4/11
	Nonintestinal failurec—survived	45.5%, n = 5/11
Gender	Male—survived	43.8%, n = 7/16	1.0000
	Female—survived	41.7%, n = 5/12
Genetic diagnosis presentd	Survived	25.0%, n = 3/12	0.0671
	Died	62.5%, n = 10/16
Perioperative factors
Age group at transplant	Adult—survived	42.9%, n = 6/14	1.0000
	Pediatric—survived	42.9%, n = 6/14
Age at transplant, median (interquartile range)	Survived, n = 12	17.0 (5.4–32.8) y	0.9630
	Died, n = 16	20.0 (2.2–36.7) y
Donor age at transplant, median (interquartile range)	Survived, n = 12	11.5 (1.6–17.5) y	0.7983
	Died, n = 16	8.0 (2.6–16.5) y
Donor to recipient age ratio, median (interquartile range)	Survived, n = 12	0.45 (0.20–0.90)	0.3156
	Died, n = 16	0.70 (0.35–1.1)
Repeat intestinal transplant	Survived	25.0%, n = 3/12	1.0000
	Died	18.8%, n = 3/16
Transplant type	Small intestine—survived	70.0%, n = 7/10	0.0631
	Liver and small intestine—survived	40.0%, n = 2/5
	Multivisceral and modified multiviscerale—survived	23.1%, n = 3/13
Liver graft included	Survived	41.7%, n = 5/12	0.2495
	Died	68.8%, n = 11/16
Splenectomy with transplantf	Survived	25.0%, n = 3/12	0.0671
	Died	62.5%, n = 10/16
Colon graft included	Survived	100%, n = 12/12	0.2381
	Died	81.2%, n = 13/16
Number of DR locus mismatches, median (interquartile range)	Survived, n = 12	2.0 (2.0–2.0)	0.3250
	Died, n = 13	2.0 (1.8–2.0)
Immunological factors
Immunosuppression induction with rabbit antithymocyte globuling	Survived	33.3%, n = 4/12	0.6908
	Died	25.0%, n = 4/16
Early secondary immunosuppression after transplanth	Received sirolimus and survived	33.3%, n = 1/3	0.8261
	Received mycophenolate mofetil and survived	25.0%, n = 1/4
	Received neither and survived	47.6%, n = 10/21
Graft rejection before onset GVHD	Survived	8.3%, n = 1/12	0.4286
	Died	0%, n = 0/16
Clinical features of GVHD
Time of onset after transplant, median (interquartile range)	Survived, n = 12	32 (12–42) d	0.2094
	Died, n = 16	48 (22–72) d
Fever present at onset	Survived	41.7%, n = 5/12	0.2495
	Died	68.8%, n = 11/16
Classic skin biopsy at onseti	Survived	22.2%, n = 2/9	0.5372
	Died	30.8%, n = 4/13
Highest biopsy grade of skin disease	Grade I—survived	0%, n = 0/1	0.9999
	Grade II—survived	30.8%, n = 4/13
	Grade III—survived	0%, n = 0/2
Absolute lymphocyte count at presentation, median (interquartile range)	Survived, n = 12	850 (650–1200)/μL	0.3888
	Died, n = 16	750 (350–1200)/μL
Absolute neutrophil count at presentation, median (interquartile range)	Survived, n = 12	7850 (2900–10 850)/μL	0.7103
	Died, n = 16	4650 (2700–10 100)/μL
Total donor peripheral blood chimerism, median (interquartile range)	Survived, n = 11	0.0 (0.0–0.0)%	0.0050
	Died, n = 14	2.5 (0.0–5.3)%
Number of disease sites at presentation, median (interquartile range)	Survived, n = 12	1.0 (1.0–2.0)	0.8540
	Died, n = 16	1.0 (1.0–2.0)
More than 1 disease site at presentation	Survived	33.3%, n = 4/12	1.0000
	Died	37.5%, n= 6/16
Number of GVHD sites emerging after treatment, median (interquartile range)	Survived, n = 12	0 (0.0–0.0)	0.0014
	Died, n = 16	1.5 (0.5–3.0)
Any GVHD site emerging after treatment	Survived	16.7%, n = 2/12	0.0063
	Died	75.0%, n = 12/16
Time of late site emergence after GVHD onset, median (interquartile range)	Survived, n = 2	153 d	0.2733
	Died, n = 12	58 (35–174) d
Total number of involved sites, median (interquartile range)	Survived, n = 12	2.0 (1.0–2.0)	0.0017
	Died, n = 16	3.0 (2.0–4.5)
Treatment of GVHD
Initial steroid response	Survived	100%, n = 11/11	1.0000
	Died	93.3%, n = 14/15
Steroid resistancej	Survived	50.0%, n = 6/12	0.0031
	Died	100%, n = 15/15
Anti-interleukin 2 receptor antibody	Survived	0%, n = 0/12	1.0000
	Died	6.2%, n = 1/16
Antitumor necrosis factor antibody	Survived	0%, n = 0/12	0.2381
	Died	18.8%, n = 3/16
Antithymocyte globulink	Survived	33.3%, n = 4/12	0.2761
	Died	56.2%, n = 9/16
Sirolimus or mycophenolate mofetill	Survived	83.3%, n = 10/12	0.6618
	Died	68.8%, n = 11/16
Extracorporeal photopheresis	Survived	0%, n = 0/12	0.0103
	Died	43.8%, n = 7/16
Ruxolitinib	Survived	0%, n = 0/12	0.4921
	Died	12.5%, n = 2/16
Elapsed time from onset GVHD to end of studym	Survived, n = 12	3.0 (2.1–4.8) y	0.0853
	Died, n = 16	6.1 (3.0–8.6) y
Complications of GVHD and treatment
Insulin therapy during treatment	Survived	33.3%, n = 4/12	0.1283
	Died	66.7%, n = 10/15
Renal replacement therapy	Survived	0%, n = 0/12	0.0031
	Died	53.3%, n = 8/15
Aspergillus infection	Survived	8.3%, n = 1/12	0.0433
	Died	46.7%, n = 7/15
Cytomegalovirus infection	Survived	8.3%, n = 1/12	0.6051
	Died	20.0%, n = 3/15
Epstein-Barr virus infection	Survived	25.0%, n = 3/12	0.6828
	Died	40.0%, n = 6/15
Pseudomonas infection	Survived	0%, n = 0/12	0.1060
	Died	26.7%, n = 4/15
Sepsis of all causes	Survived	8.3%, n = 1/12	<0.0001
	Died	93.3%, n = 14/15
New tumor developing during treatment	Survived	16.7%, n = 2/12	0.2232
	Died	43.8%, n = 7/16
Eventual remission of GVHD	Survived	100%, n = 12/12	0.0009
	Died	37.5%, n = 6/16
Graft rejection after GVHD	Survived	8.3%, n = 1/12	0.1965
	Died	31.2%, n = 5/16

Fisher exact test, Fisher-Freeman-Halton test, or Mann-Whitney test as appropriate.

Functional intestinal failure equivalent to congenital mucosal disease and dysmotility.

Nonintestinal failure equivalent to abdominal tumors and portomesenteric thrombosis, primary and secondary.

Proven by testing or assumed because of known inheritance patterns.

Multivisceral and modified multivisceral transplants in combination equivalent to splenectomy.

Splenectomy with transplant in comparison with spleen-preserving transplants: small intestine and liver-small intestine.

Rabbit antithymocyte globulin in place of basiliximab.

Sirolimus or mycophenolate mofetil given for at least 2 wk before onset of GVHD or for at least 2 wk after transplant including postoperative d 30 when GVHD absent.

Classic histopathology defined as vacuolar interface degeneration, full-thickness keratinocyte necrosis, or satellite cell necrosis.

Lack of initial response or recurrence of disease after initial response.

Rabbit antithymocyte globulin in 10 and equine antithymocyte globulin in 3.

Sirolimus in 11, mycophenolate mofetil in 8, combination of sirolimus and mycophenolate mofetil in 2.

End of study: June 30, 2020. P values in bold font denote significance at < 0.0500.

GVHD, graft vs host disease.

TABLE 5.

Univariable and multivariable Cox proportional hazards modeling of factors associated with death following GVHD after intestinal transplantation

Explanatory variable	Univariable hazard ratio (95% confidence interval)	P	Multivariable hazard ratio (95% confidence interval)	P
Pretransplant recipient factors
Genetic diagnosis presenta	2.8821 (1.0324–8.0462)	0.0433
Perioperative factors
Transplant type
Isolated intestinal transplant relative to splenectomy-associated transplantb	0.2303 (0.0628–0.8442)	0.0267
Splenectomy-associated transplantb	2.7377 (0.9916–7.5584)	0.0519
Clinical features of GVHD
Donor total lymphocyte chimerism	1.0434 (1.0030–1.0854)	0.0349
Number of GVHD sites emerging after treatment	1.3646 (1.0971–1.6972)	0.0052
No GVHD site emerging after treatment	0.1319 (0.0357–0.4870)	0.0024
Total number of involved sites	1.4275 (1.1248–1.8116)	0.0034
Complications of GVHD
Renal replacement therapy during treatment	8.9834 (2.7885–28.9413)	0.0002
Aspergillus infection during and after treatment	4.2105 (1.3687–12.9525)	0.0122
Sepsis of all types during treatment	41.5925 (5.1243–337.5959)	0.0005	37.4181 (4.5517, 307.6056)	0.0008
Nonremission of GVHD	15.9832 (3.4046–75.0349)	0.0004

Proven by testing or assumed because of known inheritance patterns.

Splenectomy-associated transplant equivalent to multivisceral and modified multivisceral transplant in combination. Modified multivisceral transplant excludes simultaneous en bloc liver transplant. P values in bold font denote significance at <0.0500.

GVHD, graft vs host disease.

Risk Factors for Occurrence of GVHD

A comparison of the 28 patients with GVHD with 206 ITx recipients without GVHD who survived at least 1 y after ITx is summarized in Table 6. As shown in Table 6, patients developing GVHD more frequently had functional IF, non-IF, and genetic diagnoses; 1 or more previous transplants; more mismatching at the HLA-DR locus; and received colon- and splenectomy-inclusive ITx. Conversely, those developing GVHD less commonly received early secondary immunosuppression with SIR or experienced graft rejection. Contrasting with HLA-DR, those developing and not developing GVHD had similar numbers of mismatches at other HLA loci, including A, B, C, DQ, DRB, Bw4, Bw6, and A and B cross-reactive groups; they also did not differ in frequency of donor HLA homozygosity. Of the 6 patients developing GVHD with a history of previous transplant, 3 received a MVTx, 2 received a LITx, and 1 received an IITx; all 6 received a colon graft. The 22 patients developing GVHD after primary ITx did not differ from retransplanted patients in distribution of variant ITx operations (P = 0.3404) or graft colon inclusion (P = 1.0).

TABLE 6.

Factors associated with occurrence of GVHD in 28 of 234 patients after intestinal transplantation

		GVHD present	GVHD absenta	P b
Demographic variables
Percentage male		57.1%, n = 16/28	57.8%, n = 119/206	1.0000
Percent adult		50.0%, n = 14/28	49.0%, n = 101/206	1.0000
Primary diseases typec	Short bowel syndrome	21.4%, n = 6/28	77.2%, n = 159/206	<0.0001
	Dysmotility	21.4%, n = 6/28	15.0%, n = 31/206
	Congenital mucosal disease	17.9%, n = 5/28	4.4%, n = 9/206
	Abdominal tumor	21.4%, n = 6/28	1.9%, n = 4/206
	Portomesenteric thrombosis, primary and secondary	17.9%, n = 5/28	1.5%, n = 3/206
Genetic diagnosis presentd		46.4%, n = 13/28	20.9%, n = 43/206	0.0077
NOD mutation present		15%, n = 3/20	23.1%, n = 42/182	0.5743
Perioperative factors
Hospitalized at transplant		11.5%, n = 3/26	14.4%, n = 24/167	1.0000
Age at transplant (y), median (interquartile range)		18.2 (2.8–33.5) y, n = 28	15.0 (1.7–42.9) y, n = 206	0.6989
Donor to recipient age ratio, median (interquartile range)		0.53 (0.29–1.0), n = 28	0.40 (0.24–0.65), n = 206	0.0534
Donor to recipient weight ratio, median (interquartile range)		0.87 (0.61 to 1.05)	0.76 (0.63–0.91)	0.2154
Transplant type	Small intestine	35.7%, n = 10/28	59.7%, n = 123/206	<0.0001
	Liver - intestine	17.9%, n = 5/28	28.6%, n = 59/206
	Multivisceral and modified multiviscerale	46.4%, n = 13/28	11.7%, n = 24/206
Liver graft included		57.1%, n = 16/28	38.3%, n = 79/206	0.0665
Colon graft included		89.3%, n = 25/28	55.8%, n = 115/206	0.0004
Splenectomy with transplantf		46.4%, n = 13/28	11.7%, n = 24/206	<0.0001
Previous transplant—any type		21.4%, n = 6/28	8.7%, n = 18/206	0.0490
Total class I mismatches, median (interquartile range)		5.0 (5.0–5.2), n = 25	5.0 (5.0–6.0), n = 170	0.4405
Number of DR locus mismatches, median (interquartile range)		2.0 (2.0–2.0), n = 25	2.0 (1.0–2.0), n = 193	0.0268
Total class II mismatches, median (interquartile range)		4.0 (4.0–5.0), n = 23	4.0 (3.0–5.0), n = 178	0.1382
Immunological factors
Panel reactive antibodies at transplant, median  (interquartile range)		0.0 (0.0–20.8) %, n = 27	0.0 (0.0–19.8) %, n = 201	0.4960
Pretreatment of donor with rabbit antithymocyte globulin		75.0%, n = 18/24	71.4%, n = 125/175	0.8126
Induction immunosuppression
	Basiliximab	71.4%, n = 20/28	69.4%, n = 143/206	0.8001
	Rabbit antithymocyte globulin	28.6%, n = 8/28	30.6%, n = 63/206
Early secondary immunosuppression after transplantg				0.0058
	Sirolimus	10.7%, n = 3/28	39.5%, n = 62/157
	Mycophenolate mofetil	14.3%, n = 4/28	12.7%, n = 20/157
	None	75.0%, n = 21/28	47.8%, n = 75/157
Absolute neutrophil count at 37 d after transplant, median  (interquartile range)		5450/μL (2700–10 850/μL), n = 28	5000/μL (3200–7300/μL), n = 130	0.6260
Absolute lymphocyte count at 37 d after transplant, median  (interquartile range)		800/μL (550–1200/μL), n = 28	1100/μL (400–2300/μL), n = 130	0.1962
Rejection within 90 d after intestinal transplant (if no GVHD)  or before GVHD		3.6%, n = 1/28	18.9%, n = 39/206	0.0572
Overall incidence of graft rejection		25.0%, n = 7/28	51.0%, n = 105/206	0.0144
Transplant outcomes
5-y graft survivalh		36.4%, n= 4/11	71.1%, n = 121/157	0.0067
5-y patient survivalh		36.4%, n = 4/11	81.8%, n = 130/159	0.0019

One-year patient survival required for inclusion in the GVHD absent cohort.

Fisher exact test, Fisher-Freeman-Halton test, or Mann-Whitney test as appropriate.

Categories consolidated into 3 composite groups for analysis including short bowel syndrome (anatomic intestinal failure), functional intestinal failure equivalent to congenital mucosal disease and dysmotility, and nonintestinal failure equivalent to abdominal tumors and portomesenteric thrombosis, primary and secondary.

Proven by testing or assumed because of known inheritance patterns.

Multivisceral and modified multivisceral transplants in combination equivalent to splenectomy. Modified multivisceral transplant excludes simultaneous en bloc liver transplant.

Splenectomy with transplant in comparison with spleen-preserving transplants: small intestine and liver-small intestine.

Sirolimus or mycophenolate mofetil given for at least 2 wk before onset of GVHD or for at least 2 wk after transplant including postoperative d 30 when GVHD absent. Ten patients receiving both drugs in this timeframe excluded from analysis.

Patients transplanted before June 30, 2015. P values in bold font denote significance at <0.0500.

GVHD, graft vs host disease; NOD, nucleotide-binding oligomerization domain.

Results of univariable and multivariable Cox modeling of factors associated with development of GVHD are summarized in Table 7; explanatory variables associated with an increased hazard of GVHD mostly paralleled greater cumulative incidences shown in Table 6. As shown in Table 7, multivariable modeling emphasized the overriding importance of original disease (non-IF, Wald’s chi-square 18.5428; functional IF, Wald’s chi-square 4.9578) and greater donor to recipient age ratio (DRAR; Wald’s chi-square 5.7501) to increased GVHD risk and of early exposure to SIR (Wald’s chi-square 5.2650) to reduced GVHD risk. Type of ITx operation was not associated with GVHD risk independent of original disease in multivariable modeling; illustrative of this finding, splenectomy-inclusive ITx was performed in 7.9% (13/165) of patients with anatomic IF, 19.6% (10/51) of patients with functional IF, and 77.8% (14/18) of patients without IF (P < 0.0001).

TABLE 7.

Univariable and multivariable Cox proportional hazard regression modeling of risks for occurrence of graft vs host disease after intestinal transplantation in patients of all ages

Explanatory variable	Univariable hazard ratio (95% confidence interval)	P	Multivariable hazard ratio (95% confidence interval)	P
Primary disease
Nonintestinal failurea relative to anatomic intestinal failure	22.0157 (8.1254–59.6515)	<0.0001	11.3181 (3.7509–34.1520)	<0.0001
Functional intestinal failureb relative to anatomic intestinal failure	7.1053 (2.6243–19.2376)	0.0001	3.9210 (1.1777–13.0542)	0.0260
Genetic diagnosisc	3.3190 (1.5773–6.9837)	0.0016
Retransplant	3.1715 (1.2798–7.8598)	0.0127
Donor to recipient age ratio	2.4316 (1.1490–5.1457)	0.0202	4.2798 (1.3041–14.0451)	0.0165
Number of DR locus mismatches	2.9843 (1.0538–8.4519)	0.0395
Transplant type
Splenectomy-associated transplantd	5.1395 (2.4448–10.8043)	<0.0001
Colon graft omission	0.1272 (0.0379–0.4265)	0.0008
Early secondary immunosuppression with sirolimuse	0.1775 (0.0529–0.5963)	0.0052	0.1750 (0.0395–0.7756)	0.0218

Nonintestinal failure consists of tumor and portomesenteric thrombosis.

Functional intestinal failure consists of congenital mucosal disease and dysmotility.

Proven by testing or assumed because of known inheritance patterns.

Splenectomy-associated transplant equivalent to multivisceral and modified multivisceral transplant in combination. Modified multivisceral transplant excludes simultaneous en bloc liver transplant.

Minimum of 14 d of treatment either immediately before onset of graft vs host disease or within first month after transplant including postoperative d 30 in those not developing graft vs host disease. Ten patients receiving both drugs in this timeframe excluded from analysis.

P values in bold font denote significance at <0.0500.

Comparison of multivariable Cox modeling of the whole GVHD group (Table 7) with adult (Table 8) and pediatric (Table 9) subgroups indicated age-associated divergence in independent GVHD hazards. Thus, the whole group association of functional IF with increased GVHD risk and of early SIR therapy with reduced GVHD risk originated from strength of these associations in the adult subgroup, whereas whole group association of DRAR with GVHD originated from this association in infants and children. Only pediatric patients incurred independently increased risks for GVHD from inclusion of a colon graft and retransplantation. A high DRAR was the most important covariate associated with GVHD in pediatric patients (Wald’s chi-square 14.4284); median DRAR in those with GVHD was 1.0 (0.43–1.2) compared with 0.33 (0.21–0.63) in those without(P = 0.0065.) Receiver operating characteristic curve analysis indicated that a DRAR equal to 0.9 was 64.3% sensitive and 90.5% specific for GVHD (P = 0.021). In contrast, the interquartile range of DRAR in the entire adult population (0.30–0.68) was comparatively narrow (pediatric to adult variance ratio = 2.0376, P < 0.001), and the median DRAR of 0.46 did not differ between adult patients who did and did not develop GVHD (P = 0.6101).

TABLE 8.

Univariable and multivariable Cox proportional hazard regression modeling of hazards for occurrence of graft vs host disease after intestinal transplantation in adults

Explanatory variable	Univariable hazard ratio (95% confidence interval)	P	Multivariable hazard ratio (95% confidence interval)	P
Primary disease
Nonintestinal failureb relative to anatomic intestinal failure	26.2683 (5.5751–123.7689)	<0.0001	20.9952 (4.4248–99.6202)	0.0001
Functional intestinal failurec relative to anatomic intestinal failure	8.5846 (1.5648–47.0964)	0.0133	15.2448 (2.7266–85.2365	0.0019
Genetic diagnosisd	2.8615 (0.9909–8.2637)	0.0520
Transplant type
Splenectomy-associated transplante	4.5962 (1.6088–13.1309)	0.0044
Liver graft inclusion	3.9134 (1.3079–11.7097)	0.0147
Early secondary immunosuppression with sirolimusf	0.1074 (0.0137–0.8406)	0.0335	0.0956 (0.0116–0.7900)	0.0293

Adults equivalent to age 18 y and above at transplant.

Nonintestinal failure consists of tumor and portomesenteric thrombosis.

Functional intestinal failure consists of congenital mucosal disease and dysmotility.

Proven by testing or assumed because of known inheritance patterns.

Splenectomy-associated transplant equivalent to multivisceral and modified multivisceral transplant in combination. Modified multivisceral transplant excludes simultaneous en bloc liver transplant.

Minimum of 14 d of treatment either immediately before onset of graft vs host disease or within first month after transplant including postoperative d 30 in those not developing graft vs host disease. Eight patients receiving both drugs in this timeframe excluded from analysis.

P values in bold font denote significance at <0.0500.

TABLE 9.

Univariable and multivariable Cox proportional hazard regression modeling of risks for occurrence of graft vs host disease after intestinal transplantation in pediatric patients

Explanatory variable	Univariable hazard ratio (95% confidence interval)	P	Multivariable hazard ratio (95% confidence interval)	P
Primary disease
Nonintestinal failureb relative to anatomic intestinal failure	22.7173 (4.9699–103.8405)	0.0001	4.3990 (1.1000–17.5924)	0.0362
Functional intestinal failurec relative to anatomic intestinal failure	6.4578 (1.8868–22.1022)	0.0030
Genetic diagnosisd	3.7073 (1.2951–10.6124)	0.0146
Retransplant	5.0418 (1.6860–15.0770)	0.0038	4.6401 (1.3974–15.4082)	0.0122
Donor to recipient age ratio	3.5809 (1.6615–7.7179)	0.0011	7.3190 (2.6206–20.4410)	0.0001
Transplant type
Splenectomy-associated transplante	5.3718 (1.8604–15.5105)	0.0019
Colon graft omission	0.2610 (0.0712–0.9570)	0.0427	0.1886 (0.0416–0.8555)	0.0306

Pediatric patients correspond to age <18 y at transplant.

Nonintestinal failure equivalent to tumor and portomesenteric thrombosis.

Functional intestinal failure equivalent to congenital mucosal disease and dysmotility.

Proven by testing or assumed because of known inheritance patterns.

Splenectomy-associated transplant equivalent to multivisceral and modified multivisceral transplant in combination. Modified multivisceral transplant excludes simultaneous en bloc liver transplant.

P values in bold font denote significance at <0.0500.

DISCUSSION

Many findings in this review of GVHD after ITx are consistent with those of previous investigations including typical presentation with rash and fever within 2 mo after ITx[8,11] and similar incidence in adult and pediatric patients.[3,32] However, prevalence of extracutaneous GVHD approximated 80% in this series, contrasting with previous estimates that have ranged between about 30% and 50%.[9,10,13,32] High incidence of GVHD involvement at extracutaneous sites, especially colon, facilitated diagnosis in individual patients. Furthermore, multiple site involvement was a hazard for reduced survival, being associated with refractoriness to successive immunosuppressive therapies[9,33] that set the stage for fatal opportunistic infection.[8-10] Notable among these infections was invasive aspergillosis that has also figured prominently in negative outcomes after HSCT.[34,35]

This study identified several factors related to the balance between donor and recipient immune function critical to development of GVHD after SOT.[3,36,37] Most prominently, GVHD after ITx tended to occur when the original disease was associated with abnormal immune function, either subtle, examples including intestinal pseudoobstruction[38] and trichohepatoenteric syndrome,[39] or severe, particularly multiple intestinal atresia syndrome.[13,40] GVHD was remarkably uncommon with a background of stand-alone short bowel. GVHD hazard was also increased by use of grafts from pediatric donors similar in age to recipients in comparison with younger donors presumably less immunocompetent.[37,41] The strong connection of DRAR to GVHD risk implies that age-related physiological disparity in immune function, like absolute recipient immunodeficiency, is highly relevant to GVHD risk. This phenomenon was not observed in adults, presumably due to greater consistency in age difference between donors and recipients in the adult cohort. However, it is notable that transplantation of liver grafts into adults from donors >20 y younger, and presumably more immunocompetent, also increases GVHD risk,[42] the mirror image of the relationship prevailing in our pediatric patients.

In some ITx recipients, potential recipient immune deficiencies favoring GVHD appeared to be acquired rather than inborn such as that associated with retransplantation,[12] although we have no explanation for restriction of this risk to pediatric patients in this study. Transience of recipient immune incompetence was also implied by occurrence of severe graft rejection in some patients generally after GVHD recovery. Like others,[9,13] we found a strong association between recipient splenectomy necessitated by MVTx and MMVTx and GVHD risk, presumably by weakening recipient defense against donor-derived alloreactive T-cell clones. However, because our practice reserves MVTx and MMVTx primarily for non-IF failure and functional IF diagnoses, multivariable regression modeling rejected splenectomy as an independent hazard for GVHD. Because of this bias, an independent effect of splenectomy on GVHD risk may not have been detected. GVHD risk was independently increased by colon graft inclusion that was anticipated by an early experimental ITx model.[43] The relatively greater colon lymphocyte mass in infants and children compared with older persons[44] may explain confinement of this risk to pediatric patients and emphasizes the need to weigh risks of graft colon inclusion against the clear benefits,[45] particularly in younger ITx candidates.

Attempts to reduce GVHD risk by weakening donor-derived immune function with r-ATG during ITx organ procurement is a long-established practice. In this study, r-ATG failed in this objective, possibly due to insufficient time to achieve meaningful donor lymphocyte depletion[46] or to intrinsic resistance of key donor memory T cells to r-ATG.[47] Failure of induction immunosuppression with r-ATG to reduce GVHD incidence compared with basiliximab may be another expression of that resistance. We are reassessing r-ATG in donor procurement to ascertain if a subset of patients can be identified for whom donor r-ATG might yet prove beneficial. In contrast with r-ATG, SIR given during the first month after ITx reduced GVHD risk in adults. Given the efficacy of SIR in reducing ITx rejection risk,[48] its prophylactic value against GVHD provides an additional rationale for early employment after ITx when risks of both acute rejection and GVHD are at their highest. There is evidence that mismatch at the HLA-DR locus is related to graft rejection,[49,50] whereas in this study, the HLA-DR locus was associated with GVHD. Although magnitude of GVHD risk from HLA-DR mismatch was small, this commonality further emphasizes the dynamic, 2-way immune balance that prevails after ITx.[37]

Limitations of this study include primary reliance on routine clinical assessment including standard histopathology to diagnose GVHD without proof of local tissue chimerism or peripheral blood T-cell chimerism data in most cases, although magnitude of T-cell chimerism in those with and without GVHD overlaps.[10,37] Conversely, there was no accounting of suspected GVHD cases ultimately rejected on clinical or immunological grounds to compare with affirmative GVHD diagnoses. Furthermore, the uncontrolled nature of treatment undermined identification and optimal employment of potentially useful interventions. Clinical management practices inevitably evolved during the almost 17-y study period, potentially altering GVHD expression.

CONCLUSIONS AND LESSONS LEARNED

GVHD risk after ITx was related more to original disease than to ITx variant operation in patients of all ages. Pretreatment of donors with r-ATG before graft recovery did not reduce GVHD risk. In pediatric but not adult patients, use of grafts from donors significantly younger than intended recipients reduced GVHD risk, whereas including colon with the ITx and repeat transplantation increased GVHD risk. In adult but not pediatric patients, use of SIR soon after ITx reduced GVHD risk, reason for the differential effect based on age being unclear.

Established therapies for GVHD in SOT are based on practices in HSCT. Corticosteroids constitute first-line therapy, and with steroid refractoriness, other immunosuppressives with inconsistent efficacy are used that further predispose to infection.[5] Before recent regulatory agency approval of the Janus kinase signal transduction inhibitor ruxolitinib for corticosteroid-refractory GVHD after HSCT,[6] 2 patients in this study received ruxolitinib off-label in a final but unsuccessful effort to control GVHD unresponsive to numerous therapies including r-ATG.[51] In both cases, delayed employment likely contributed to ruxolitinib failure in the setting of advanced disease and patient debility. We now use ruxolitinib as second-line therapy for GVHD once corticosteroid refractoriness has been established on the presumption that earlier use in the GVHD course shall increase probability of extended remission with reduced risk of morbid and fatal complications.