Compartmentalized gut lymph node drainage dictates adaptive immune responses
Autor: | Daria Esterházy, Paul A. Muller, Tiago B. R. Castro, Luka Mesin, Ainsley Lockhart, Ana Maria Caetano Faria, Mahmoud ElJalby, Maria C. C. Canesso, Daniel Mucida |
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Rok vydání: | 2019 |
Předmět: |
Male
0301 basic medicine Duodenum T-Lymphocytes T cell Adaptive Immunity Biology Article Mice 03 medical and health sciences 0302 clinical medicine Immune system Antigen Cell Movement medicine Animals Microbiome Rats Wistar Mouth Multidisciplinary Cell Polarity FOXP3 Cell Differentiation Dendritic Cells Dendritic cell Acquired immune system Rats 3. Good health Mice Inbred C57BL Intestines 030104 developmental biology medicine.anatomical_structure Lymphatic system 030220 oncology & carcinogenesis CD4 Antigens Immunology Drainage Female Lymph Nodes Stromal Cells |
Zdroj: | Nature |
ISSN: | 1476-4687 0028-0836 |
DOI: | 10.1038/s41586-019-1125-3 |
Popis: | The intestinal immune system has the challenging task of tolerating foreign nutrients and the commensal microbiome, while excluding or eliminating ingested pathogens. Failure of this balance leads to conditions such as inflammatory bowel diseases, food allergies and invasive gastrointestinal infections1. Multiple immune mechanisms are therefore in place to maintain tissue integrity, including balanced generation of effector T (TH) cells and FOXP3+ regulatory T (pTreg) cells, which mediate resistance to pathogens and regulate excessive immune activation, respectively1–4. The gut-draining lymph nodes (gLNs) are key sites for orchestrating adaptive immunity to luminal perturbations5–7. However, it is unclear how they simultaneously support tolerogenic and inflammatory reactions. Here we show that gLNs are immunologically specific to the functional gut segment that they drain. Stromal and dendritic cell gene signatures and polarization of T cells against the same luminal antigen differ between gLNs, with the proximal small intestine-draining gLNs preferentially giving rise to tolerogenic responses and the distal gLNs to pro-inflammatory T cell responses. This segregation permitted the targeting of distal gLNs for vaccination and the maintenance of duodenal pTreg cell induction during colonic infection. Conversely, the compartmentalized dichotomy was perturbed by surgical removal of select distal gLNs and duodenal infection, with effects on both lymphoid organ and tissue immune responses. Our findings reveal that the conflict between tolerogenic and inflammatory intestinal responses is in part resolved by discrete gLN drainage, and encourage antigen targeting to specific gut segments for therapeutic immune modulation. Immune responses in the gut and associated draining lymph nodes differ between tolerogenic and inflammatory depending on their anatomical location. |
Databáze: | OpenAIRE |
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