Massachusetts Institute of Technology
Commensal-specific immune responses at the intestinal mucosa
Abstract
dc:description.abstractThe intestinal mucosa harbors a dense community of microbes that breaks down polysaccharides indigestible by the host, synthesizes essential vitamins, stimulates maturation of the immune system, and outcompetes the growth of pathogenic species. In return, the host provides commensals with a habitat rich in energy derived from ingested food. The intestinal immune system faces the daunting task of maintaining homeostasis despite the enormous load and diversity of antigens present at this site. Failure to maintain this balance has dramatic consequences and can cause food allergies, inflammatory bowel disease or invasive infections. Peripherally-induced Foxp3⁺-regulatory T cells (pTregs) maintain immune homeostasis at the intestinal mucosa by regulating effector T cell responses against dietary antigens and microbes.
Degree
thesis:*- Name thesis:degree_name
- Doctoral
- Department dc:contributor.department
- Massachusetts Institute of Technology. Department of Biology
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2020
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Bousbaine, Djenet.
- Advisor dc:contributor.advisor
-
- Hidde Ploegh.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- https://hdl.handle.net/1721.1/129900
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/129900