4.6 Article

Remission of peanut allergy is associated with rewiring of allergen-driven T helper 2-related gene networks

期刊

ALLERGY
卷 77, 期 10, 页码 3015-3027

出版社

WILEY
DOI: 10.1111/all.15324

关键词

CD4(+) T cells; food oral immunotherapy; network analysis; remission of allergy; sustained unresponsiveness

资金

  1. Murdoch Children's Research Institute
  2. Perpetual Philanthropy [493]
  3. Food Allergy and Anaphylaxis Network
  4. Financial Markets Foundation for Children
  5. Cass Foundation
  6. National Health and Medical Research Council [1029690, 1129996]
  7. Simon Lee Foundation
  8. Victorian Government's Operational Infrastructure Support Program

向作者/读者索取更多资源

The immunological changes underlying remission following peanut oral immunotherapy are mediated by reprogramming of T helper 2-associated gene networks in the CD4(+) T cell compartment. These findings provide insight into immune mechanisms driving the acquisition of remission following oral immunotherapy, paving the way for the development of improved approaches to induce remission/sustained unresponsiveness in patients with food allergy.
Background The immunological changes underpinning acquisition of remission (also called sustained unresponsiveness) following food immunotherapy remain poorly defined. Limited access to effective therapies and biosamples from treatment responders has prevented progress. Probiotic peanut oral immunotherapy is highly effective at inducing remission, providing an opportunity to investigate immune changes. Methods Using a systems biology approach, we examined gene co-expression network patterns in peanut-specific CD4(+) T cell responses before and after probiotic and peanut oral immunotherapy in subjects enrolled in the PPOIT-001 randomized trial: Responders who attained remission (n = 16), placebo-treated who remained allergic (n = 16). Results Acquisition of remission was associated with rewiring of gene network patterns, which was characterized by integration of T helper 2 and interferon signalling modules, markedly reduced T helper 2 gene connectivity, and shutdown in co-expression activity between T helper 2 effectors and cell cycle regulators. Conclusion The immunological changes underlying remission following peanut oral immunotherapy are mediated by reprogramming of T helper 2-associated gene networks in the CD4(+) T cell compartment. Findings provide insight into immune mechanisms driving the acquisition of remission following oral immunotherapy, paving the way for the development of improved approaches to induce remission/sustained unresponsiveness in patients with food allergy.

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