CD4+ NKT cells, but not conventional CD4+ T cells, are required to generate efferent CD8+ T regulatory cells following antigen inoculation in an immune-privileged site - PubMed (original) (raw)
Comparative Study
. 2003 Aug 1;171(3):1266-71.
doi: 10.4049/jimmunol.171.3.1266.
Affiliations
- PMID: 12874214
- DOI: 10.4049/jimmunol.171.3.1266
Comparative Study
CD4+ NKT cells, but not conventional CD4+ T cells, are required to generate efferent CD8+ T regulatory cells following antigen inoculation in an immune-privileged site
Takahiko Nakamura et al. J Immunol. 2003.
Abstract
Following inoculation of Ag into the anterior chamber (a.c.), systemic tolerance develops that is mediated in part by Ag-specific efferent CD8(+) T regulatory (Tr) cells. This model of tolerance is called a.c.-associated immune deviation. The generation of the efferent CD8(+) Tr cell in a.c.-associated immune deviation is dependent on IL-10-producing, CD1d-restricted, invariant Valpha14(+) NKT (iNKT) cells. The iNKT cell subpopulations are either CD4(+) or CD4(-)CD8(-) double negative. This report identifies the subpopulation of iNKT cells that is important for induction of the efferent Tr cell. Because MHC class II(-/-) (class II(-/-)) mice generate efferent Tr cells following a.c. inoculation, we conclude that conventional CD4(+) T cells are not needed for the development of efferent CD8(+) T cells. Furthermore, Ab depletion of CD4(+) cells in both wild-type mice (remove both conventional and CD4(+) NKT cells) and class II(-/-) mice (remove CD4(+) NKT cells) abrogated the generation of Tr cells. We conclude that CD4(+) NKT cells, but not the class II molecule or conventional CD4(+) T cells, are required for generation of efferent CD8(+) Tr cells following Ag introduction into the eye. Understanding the mechanisms that lead to the generation of efferent CD8(+) Tr cells may lead to novel immunotherapy for immune inflammatory diseases.
Similar articles
- NKT cell-derived RANTES recruits APCs and CD8+ T cells to the spleen during the generation of regulatory T cells in tolerance.
Faunce DE, Stein-Streilein J. Faunce DE, et al. J Immunol. 2002 Jul 1;169(1):31-8. doi: 10.4049/jimmunol.169.1.31. J Immunol. 2002. PMID: 12077225 - NKT cells enhance CD4+ and CD8+ T cell responses to soluble antigen in vivo through direct interaction with dendritic cells.
Hermans IF, Silk JD, Gileadi U, Salio M, Mathew B, Ritter G, Schmidt R, Harris AL, Old L, Cerundolo V. Hermans IF, et al. J Immunol. 2003 Nov 15;171(10):5140-7. doi: 10.4049/jimmunol.171.10.5140. J Immunol. 2003. PMID: 14607913 - Mechanisms of peripheral tolerance following intracameral inoculation are independent of IL-13 or STAT6.
Nakamura T, Terajewicz A, Stein-Streilein J. Nakamura T, et al. J Immunol. 2005 Aug 15;175(4):2643-6. doi: 10.4049/jimmunol.175.4.2643. J Immunol. 2005. PMID: 16081840 - The enigma of CD4-lineage specification.
Xiong Y, Bosselut R. Xiong Y, et al. Eur J Immunol. 2011 Mar;41(3):568-74. doi: 10.1002/eji.201041098. Epub 2011 Feb 10. Eur J Immunol. 2011. PMID: 21341258 Free PMC article. Review. - iNKT cells in allergic disease.
Meyer EH, DeKruyff RH, Umetsu DT. Meyer EH, et al. Curr Top Microbiol Immunol. 2007;314:269-91. doi: 10.1007/978-3-540-69511-0_11. Curr Top Microbiol Immunol. 2007. PMID: 17593665 Review.
Cited by
- Probiotic treatment with viable α-galactosylceramide-producing Bacteroides fragilis reduces diabetes incidence in female nonobese diabetic mice.
Hansen CHF, Jozipovic D, Zachariassen LF, Nielsen DS, Hansen AK, Buschard K. Hansen CHF, et al. J Diabetes. 2024 Aug;16(8):e13593. doi: 10.1111/1753-0407.13593. J Diabetes. 2024. PMID: 39136533 Free PMC article. - Sex, T Cells, and the Microbiome in Natural ABO Antibody Production in Mice.
Adam I, Motyka B, Tao K, Jeyakanthan M, Alegre ML, Cowan PJ, West LJ. Adam I, et al. Transplantation. 2023 Nov 1;107(11):2353-2363. doi: 10.1097/TP.0000000000004658. Epub 2023 Jun 8. Transplantation. 2023. PMID: 37871273 Free PMC article. - The iNKT Cell-Macrophage Axis in Homeostasis and Disease.
Cruz MS, Loureiro JP, Oliveira MJ, Macedo MF. Cruz MS, et al. Int J Mol Sci. 2022 Jan 31;23(3):1640. doi: 10.3390/ijms23031640. Int J Mol Sci. 2022. PMID: 35163561 Free PMC article. Review. - The Research Progress in Immunotherapy of Tuberculosis.
Mi J, Liang Y, Liang J, Gong W, Wang S, Zhang J, Li Z, Wu X. Mi J, et al. Front Cell Infect Microbiol. 2021 Nov 15;11:763591. doi: 10.3389/fcimb.2021.763591. eCollection 2021. Front Cell Infect Microbiol. 2021. PMID: 34869066 Free PMC article. Review. - Cellular and Molecular Mechanisms of Anterior Chamber-Associated Immune Deviation (ACAID): What We Have Learned from Knockout Mice.
Vendomèle J, Khebizi Q, Fisson S. Vendomèle J, et al. Front Immunol. 2017 Nov 30;8:1686. doi: 10.3389/fimmu.2017.01686. eCollection 2017. Front Immunol. 2017. PMID: 29250068 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials