Successful immunotherapy induces previously unidentified allergen-specific CD4+T-cell subsets

被引:111
作者
Ryan, John F. [1 ]
Hovde, Rachel [1 ]
Glanville, Jacob [1 ]
Lyu, Shu-Chen [1 ]
Ji, Xuhuai [1 ]
Gupta, Sheena [1 ]
Tibshirani, Robert J. [2 ,3 ]
Jay, David C. [1 ]
Boyd, Scott D. [1 ,4 ]
Chinthrajah, R. Sharon [1 ]
Davis, Mark M. [1 ,5 ,6 ]
Galli, Stephen J. [1 ,4 ,5 ]
Maecker, Holden T. [1 ,5 ]
Nadeau, Kari C. [1 ]
机构
[1] Stanford Univ, Sean N Parker Ctr Allergy & Asthma Res, Pulm & Crit Care Med, Inst Immun Transplantat & Infect Dis, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Stat, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Microbiol & Immunol, Sch Med, Stanford, CA 94305 USA
[6] Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
immunotherapy; T cells; gene expression; tolerance; anergy; CD4(+) T-CELLS; PEANUT ORAL IMMUNOTHERAPY; MOLECULAR-MECHANISMS; IMMUNE TOLERANCE; TGF-BETA; DIFFERENTIATION; DESENSITIZATION; ACTIVATION; EXPRESSION; INDUCTION;
D O I
10.1073/pnas.1520180113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Allergen immunotherapy can desensitize even subjects with potentially lethal allergies, but the changes induced in T cells that underpin successful immunotherapy remain poorly understood. In a cohort of peanut-allergic participants, we used allergen-specific T-cell sorting and single-cell gene expression to trace the transcriptional "road-map" of individual CD4+ T cells throughout immunotherapy. We found that successful immunotherapy induces allergen-specific CD4+ T cells to expand and shift toward an "anergic" Th2 T-cell phenotype largely absent in both pretreatment participants and healthy controls. These findings show that sustained success, even after immunotherapy is withdrawn, is associated with the induction, expansion, and maintenance of immunotherapy-specific memory and naive T-cell phenotypes as early as 3 mo into immunotherapy. These results suggest an approach for immune monitoring participants undergoing immunotherapy to predict the success of future treatment and could have implications for immunotherapy targets in other diseases like cancer, autoimmune disease, and transplantation.
引用
收藏
页码:E1286 / E1295
页数:10
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