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CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice
Group 1 CD1 (CD1a, CD1b, and CD1c)–restricted T cells recognize mycobacterial lipid antigens and are found at higher frequencies in Mycobacterium tuberculosis (Mtb)–infected individuals. However, their role and dynamics during infection remain unknown because of the lack of a suitable small animal m...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768849/ https://www.ncbi.nlm.nih.gov/pubmed/19808251 http://dx.doi.org/10.1084/jem.20090898 |
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author | Felio, Kyrie Nguyen, Hanh Dascher, Christopher C. Choi, Hak-Jong Li, Sha Zimmer, Michael I. Colmone, Angela Moody, D. Branch Brenner, Michael B. Wang, Chyung-Ru |
author_facet | Felio, Kyrie Nguyen, Hanh Dascher, Christopher C. Choi, Hak-Jong Li, Sha Zimmer, Michael I. Colmone, Angela Moody, D. Branch Brenner, Michael B. Wang, Chyung-Ru |
author_sort | Felio, Kyrie |
collection | PubMed |
description | Group 1 CD1 (CD1a, CD1b, and CD1c)–restricted T cells recognize mycobacterial lipid antigens and are found at higher frequencies in Mycobacterium tuberculosis (Mtb)–infected individuals. However, their role and dynamics during infection remain unknown because of the lack of a suitable small animal model. We have generated human group 1 CD1 transgenic (hCD1Tg) mice that express all three human group 1 CD1 isoforms and support the development of group 1 CD1–restricted T cells with diverse T cell receptor usage. Both mycobacterial infection and immunization with Mtb lipids elicit group 1 CD1–restricted Mtb lipid–specific T cell responses in hCD1Tg mice. In contrast to CD1d-restricted NKT cells, which rapidly respond to initial stimulation but exhibit anergy upon reexposure, group 1 CD1–restricted T cells exhibit delayed primary responses and more rapid secondary responses, similar to conventional T cells. Collectively, our data demonstrate that group 1 CD1–restricted T cells participate in adaptive immune responses upon mycobacterial infection and could serve as targets for the development of novel Mtb vaccines. |
format | Text |
id | pubmed-2768849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27688492010-04-26 CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice Felio, Kyrie Nguyen, Hanh Dascher, Christopher C. Choi, Hak-Jong Li, Sha Zimmer, Michael I. Colmone, Angela Moody, D. Branch Brenner, Michael B. Wang, Chyung-Ru J Exp Med Article Group 1 CD1 (CD1a, CD1b, and CD1c)–restricted T cells recognize mycobacterial lipid antigens and are found at higher frequencies in Mycobacterium tuberculosis (Mtb)–infected individuals. However, their role and dynamics during infection remain unknown because of the lack of a suitable small animal model. We have generated human group 1 CD1 transgenic (hCD1Tg) mice that express all three human group 1 CD1 isoforms and support the development of group 1 CD1–restricted T cells with diverse T cell receptor usage. Both mycobacterial infection and immunization with Mtb lipids elicit group 1 CD1–restricted Mtb lipid–specific T cell responses in hCD1Tg mice. In contrast to CD1d-restricted NKT cells, which rapidly respond to initial stimulation but exhibit anergy upon reexposure, group 1 CD1–restricted T cells exhibit delayed primary responses and more rapid secondary responses, similar to conventional T cells. Collectively, our data demonstrate that group 1 CD1–restricted T cells participate in adaptive immune responses upon mycobacterial infection and could serve as targets for the development of novel Mtb vaccines. The Rockefeller University Press 2009-10-26 /pmc/articles/PMC2768849/ /pubmed/19808251 http://dx.doi.org/10.1084/jem.20090898 Text en © 2009 Felio et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article Felio, Kyrie Nguyen, Hanh Dascher, Christopher C. Choi, Hak-Jong Li, Sha Zimmer, Michael I. Colmone, Angela Moody, D. Branch Brenner, Michael B. Wang, Chyung-Ru CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice |
title | CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice |
title_full | CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice |
title_fullStr | CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice |
title_full_unstemmed | CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice |
title_short | CD1-restricted adaptive immune responses to Mycobacteria in human group 1 CD1 transgenic mice |
title_sort | cd1-restricted adaptive immune responses to mycobacteria in human group 1 cd1 transgenic mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768849/ https://www.ncbi.nlm.nih.gov/pubmed/19808251 http://dx.doi.org/10.1084/jem.20090898 |
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