Environmental enteric dysfunction induces regulatory T cells that inhibit local CD4+T cell responses and impair oral vaccine efficacy

被引:38
作者
Bhattacharjee, Amrita [1 ]
Burr, Ansen H. P. [1 ,2 ]
Overacre-Delgoffe, Abigail E. [1 ]
Tometich, Justin T. [1 ]
Yang, Deyi [1 ,3 ]
Huckestein, Brydie R. [2 ]
Linehan, Jonathan L. [4 ,6 ]
Spencer, Sean P. [4 ,7 ]
Hall, Jason A. [4 ,8 ]
Harrison, Oliver J. [4 ,9 ]
da Fonseca, Denise Morais [4 ,10 ]
Norton, Elizabeth B. [5 ]
Belkaid, Yasmine [4 ]
Hand, Timothy W. [1 ,2 ]
机构
[1] Univ Pittsburgh, UPMC Childrens Hosp Pittsburgh, RK Mellon Inst Pediat Res, Pediat Dept, Pittsburgh, PA 15224 USA
[2] Univ Pittsburgh, Sch Med, Dept Immunol, Program Microbiol & Immunol, Pittsburgh, PA 15261 USA
[3] Cent South Univ, Xiangya Sch Med, Changsha, Peoples R China
[4] NIAID, Metaorganism Immun Sect, Lab Immune Syst Biol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[5] Tulane Univ, Sch Med, Dept Microbiol & Immunol, 1430 Tulane Ave, New Orleans, LA 70112 USA
[6] Genentech Inc, San Francisco, CA 94080 USA
[7] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Palo Alto, CA 94304 USA
[8] ArsenalBio Inc, San Francisco, CA USA
[9] Benaroya Res Inst, Seattle, WA USA
[10] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会; 美国国家卫生研究院; 美国安德鲁·梅隆基金会;
关键词
INVASIVE ESCHERICHIA-COLI; IMMUNE-RESPONSES; MUCOSAL IMMUNITY; RETINOIC ACID; TH17; CELLS; GUT; MICROBIOTA; IGA; COLONIZATION; ENTEROPATHY;
D O I
10.1016/j.immuni.2021.07.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Environmental enteric dysfunction (EED) is a gastrointestinal inflammatory disease caused by malnutrition and chronic infection. EED is associated with stunting in children and reduced efficacy of oral vaccines. To study the mechanisms of oral vaccine failure during EED, we developed a microbiota- and diet-dependent mouse EED model. Analysis of E. coli-labile toxin vaccine-specific CD4(+) T cells in these mice revealed impaired CD4(+) T cell responses in the small intestine and but not the lymph nodes. EED mice exhibited increased frequencies of small intestine-resident ROR gamma T(+)FOXP3(+) regulatory T (Treg) cells. Targeted deletion of ROR gamma T from Treg cells restored small intestinal vaccine-specific CD4 T cell responses and vaccine-mediated protection upon challenge. However, ablation of ROR gamma T(+)FOXP3(+) Treg cells made mice more susceptible to EED-induced stunting. Our findings provide insight into the poor efficacy of oral vaccines in EED and highlight how ROR gamma T(+)FOXP3(+) Treg cells can regulate intestinal immunity while leaving systemic responses intact.
引用
收藏
页码:1745 / +
页数:20
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