Literature DB >> 33708195

CpG Adjuvant in Allergen-Specific Immunotherapy: Finding the Sweet Spot for the Induction of Immune Tolerance.

Guillem Montamat1,2, Cathy Leonard1, Aurélie Poli1, Ludger Klimek3, Markus Ollert1,4.   

Abstract

Prevalence and incidence of IgE-mediated allergic diseases have increased over the past years in developed and developing countries. Allergen-specific immunotherapy (AIT) is currently the only curative treatment available for allergic diseases that has long-term efficacy. Although AIT has been proven successful as an immunomodulatory therapy since its beginnings, it still faces several unmet needs and challenges today. For instance, some patients can experience severe side effects, others are non-responders, and prolonged treatment schedules can lead to lack of patient adherence and therapy discontinuation. A common strategy to improve AIT relies on the use of adjuvants and immune modulators to boost its effects and improve its safety. Among the adjuvants tested for their clinical efficacy, CpG oligodeoxynucleotide (CpG-ODN) was investigated with limited success and without reaching phase III trials for clinical allergy treatment. However, recently discovered immune tolerance-promoting properties of CpG-ODN place this adjuvant again in a prominent position as an immune modulator for the treatment of allergic diseases. Indeed, it has been shown that the CpG-ODN dose and concentration are crucial in promoting immune regulation through the recruitment of pDCs. While low doses induce an inflammatory response, high doses of CpG-ODN trigger a tolerogenic response that can reverse a pre-established allergic milieu. Consistently, CpG-ODN has also been found to stimulate IL-10 producing B cells, so-called B regulatory cells (Bregs). Accordingly, CpG-ODN has shown its capacity to prevent and revert allergic reactions in several animal models showing its potential as both preventive and active treatment for IgE-mediated allergy. In this review, we describe how CpG-ODN-based therapies for allergic diseases, despite having shown limited success in the past, can still be exploited further as an adjuvant or immune modulator in the context of AIT and deserves additional attention. Here, we discuss the past and current knowledge, which highlights CpG-ODN as a potential adjuvant to be reevaluated for the enhancement of AIT when used in appropriate conditions and formulations.
Copyright © 2021 Montamat, Leonard, Poli, Klimek and Ollert.

Entities:  

Keywords:  CpG-oligonucleotides; allergen-specific immunotherapy; allergy; immune tolerance; tolerance induction

Mesh:

Substances:

Year:  2021        PMID: 33708195      PMCID: PMC7940844          DOI: 10.3389/fimmu.2021.590054

Source DB:  PubMed          Journal:  Front Immunol        ISSN: 1664-3224            Impact factor:   7.561


  216 in total

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2.  The circadian clock controls toll-like receptor 9-mediated innate and adaptive immunity.

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3.  The adaptor molecule MyD88 activates PI-3 kinase signaling in CD4+ T cells and enables CpG oligodeoxynucleotide-mediated costimulation.

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4.  The novel synthetic immune response modifier R-848 (Resiquimod) shifts human allergen-specific CD4+ TH2 lymphocytes into IFN-gamma-producing cells.

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Journal:  J Allergy Clin Immunol       Date:  2003-02       Impact factor: 10.793

5.  Cutting edge: CpG oligonucleotides induce splenic CD19+ dendritic cells to acquire potent indoleamine 2,3-dioxygenase-dependent T cell regulatory functions via IFN Type 1 signaling.

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6.  Short- and long-term changes in gene expression mediated by the activation of TLR9.

Authors:  Sven Klaschik; Debra Tross; Hidekazu Shirota; Dennis M Klinman
Journal:  Mol Immunol       Date:  2009-12-14       Impact factor: 4.407

7.  CpG motifs of bacterial DNA exacerbate colitis of dextran sulfate sodium-treated mice.

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Journal:  Eur J Immunol       Date:  2002-07       Impact factor: 5.532

8.  Immunomodulatory effects of viral TLR ligands on experimental asthma depend on the additive effects of IL-12 and IL-10.

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Journal:  J Immunol       Date:  2007-06-15       Impact factor: 5.422

9.  Co-delivery of allergen epitope fragments and R848 inhibits food allergy by inducing tolerogenic dendritic cells and regulatory T cells.

Authors:  Jingyi Hong; Xiaojun Xiao; Qichan Gao; Shanshan Li; Bei Jiang; Xizhuo Sun; Pixin Ran; Pingchang Yang
Journal:  Int J Nanomedicine       Date:  2019-08-30

10.  Dendritic Cells Expressing MyD88 Molecule Are Necessary and Sufficient for CpG-Mediated Inhibition of IgE Production In Vivo.

Authors:  Ricardo W Alberca Custodio; Luciana Mirotti; Eliane Gomes; Fernanda P B Nunes; Raquel S Vieira; Luís Graça; Rafael R Almeida; Niels O S Câmara; Momtchilo Russo
Journal:  Cells       Date:  2019-09-28       Impact factor: 6.600

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  4 in total

1.  Identification of Robust Biomarkers for Early Predicting Efficacy of Subcutaneous Immunotherapy in Children With House Dust Mite-Induced Allergic Rhinitis by Multiple Cytokine Profiling.

Authors:  Shaobing Xie; Ruohao Fan; Qingping Tang; Xiao Cai; Hua Zhang; Fengjun Wang; Shumin Xie; Kelei Gao; Junyi Zhang; Zhihai Xie; Weihong Jiang
Journal:  Front Immunol       Date:  2022-01-12       Impact factor: 7.561

2.  Free Feeding of CpG-Oligodeoxynucleotide Particles Prophylactically Attenuates Allergic Airway Inflammation and Hyperresponsiveness in Mice.

Authors:  Takuma Okajima; Suguru Shigemori; Fu Namai; Tasuku Ogita; Takashi Sato; Takeshi Shimosato
Journal:  Front Immunol       Date:  2021-11-19       Impact factor: 7.561

Review 3.  The role of LPS and CpG in the farm effect against allergies, and beyond.

Authors:  Vivian I V Gerretsen; Martijn J Schuijs
Journal:  Allergol Select       Date:  2022-03-29

Review 4.  Inhalative Nanoparticulate CpG Immunotherapy in Severe Equine Asthma: An Innovative Therapeutic Concept and Potential Animal Model for Human Asthma Treatment.

Authors:  John Klier; Sebastian Fuchs; Gerhard Winter; Heidrun Gehlen
Journal:  Animals (Basel)       Date:  2022-08-16       Impact factor: 3.231

  4 in total

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