Bifidobacterium infantis associates with T cell immunity in human infants and is sufficient to enhance antigen-specific T cells in mice

婴儿双歧杆菌与人类婴儿的 T 细胞免疫有关,并足以增强小鼠的抗原特异性 T 细胞

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作者:Donald D Nyangahu, Anna-Ursula Happel, Jerome Wendoh, Agano Kiravu, Yuli Wang, Colin Feng, Courtney Plumlee, Sara Cohen, Bryan P Brown, Danijel Djukovic, Tariq Ganief, Melanie Gasper, Daniel Raftery, Jonathan M Blackburn, Nancy L Allbritton, Clive M Gray, Jisun Paik, Kevin B Urdahl, Heather B Jaspan

Abstract

Bacille Calmette-Guerin (BCG) vaccine can elicit good TH1 responses in neonates. We hypothesized that the pioneer gut microbiota affects vaccine T cell responses. Infants who are HIV exposed but uninfected (iHEU) display an altered immunity to vaccination. BCG-specific immune responses were analyzed at 7 weeks of age in iHEU, and responses were categorized as high or low. Bifidobacterium longum subsp. infantis was enriched in the stools of high responders, while Bacteroides thetaiotaomicron was enriched in low responders at time of BCG vaccination. Neonatal germ-free or SPF mice orally gavaged with live B. infantis exhibited significantly higher BCG-specific T cells compared with pups gavaged with B. thetaiotaomicron. B. infantis and B. thetaiotaomicron differentially affected stool metabolome and colonic transcriptome. Human colonic epithelial cells stimulated with B. infantis induced a unique gene expression profile versus B. thetaiotaomicron. We thus identified a causal role of B. infantis in early-life antigen-specific immunity.

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