T-cell activation in the curious world of the intestinal intraepithelial lymphocyte
- PMID: 15531773
- DOI: 10.1385/IR:30:3:327
T-cell activation in the curious world of the intestinal intraepithelial lymphocyte
Abstract
In conventional terms, when T cells encounter appropriate stimuli, they are induced to undergo molecular and physical changes that confer upon them a state of activation. Once initiated, activation generally results in a state of full T-cell responsiveness in an all-or-none manner. Uniquely, however, the intestinal intraepithelial lymphocytes (IELs) bear features that are decidedly different from those of T cells located throughout other immunological compartments in that they exhibit some but not all properties of activated T cells, yet they can be induced to move further into activation provided appropriate costimulatory signals have been received. IEL costimulatory molecules some of which are constitutively expressed, whereas others are upregulated following T-cell receptor (TCR)/CD3 stimulation appear to hold the key to determining the nature and magnitude of the activational process. A system of activation such as this in the intestine would be expected to have great immunological protective value for the host because it would provide an untrammeled process of T-cell activation at a barrier site where the level of antigen exposure is consistently high. Clearly, however, mechanisms must be in place to insure that the IEL activation process is not inadvertently breached. These and other issues central to the operational workings of the intestinal immune system are elaborated in this article, and a model is presented in which IEL activation can be viewed as a layered, three-stage activational process.
Similar articles
-
Proliferative properties of murine intestinal intraepithelial lymphocytes (IEL): IEL expressing TCR alpha beta or TCR tau delta are largely unresponsive to proliferative signals mediated via conventional stimulation of the CD3-TCR complex.Int Immunol. 1991 Jun;3(6):563-9. doi: 10.1093/intimm/3.6.563. Int Immunol. 1991. PMID: 1832293
-
T-cell activation in the intestinal mucosa.Immunol Rev. 2007 Feb;215:189-201. doi: 10.1111/j.1600-065X.2006.00471.x. Immunol Rev. 2007. PMID: 17291289 Free PMC article. Review.
-
Multiple levels of activation of murine CD8(+) intraepithelial lymphocytes defined by OX40 (CD134) expression: effects on cell-mediated cytotoxicity, IFN-gamma, and IL-10 regulation.J Immunol. 2001 Dec 15;167(12):6717-23. doi: 10.4049/jimmunol.167.12.6717. J Immunol. 2001. PMID: 11739485
-
Most murine CD8+ intestinal intraepithelial lymphocytes are partially but not fully activated T cells.J Immunol. 2002 Nov 1;169(9):4717-22. doi: 10.4049/jimmunol.169.9.4717. J Immunol. 2002. PMID: 12391179
-
Costimulation of T cells by OX40, 4-1BB, and CD27.Cytokine Growth Factor Rev. 2003 Jun-Aug;14(3-4):265-73. doi: 10.1016/s1359-6101(03)00025-x. Cytokine Growth Factor Rev. 2003. PMID: 12787564 Review.
Cited by
-
Gut environment-induced intraepithelial autoreactive CD4(+) T cells suppress central nervous system autoimmunity via LAG-3.Nat Commun. 2016 May 20;7:11639. doi: 10.1038/ncomms11639. Nat Commun. 2016. PMID: 27198196 Free PMC article.
-
GLP-1 and GLP-2 Orchestrate Intestine Integrity, Gut Microbiota, and Immune System Crosstalk.Microorganisms. 2022 Oct 19;10(10):2061. doi: 10.3390/microorganisms10102061. Microorganisms. 2022. PMID: 36296337 Free PMC article. Review.
-
Th17 cytokines and the gut mucosal barrier.J Clin Immunol. 2010 Mar;30(2):196-203. doi: 10.1007/s10875-010-9368-7. Epub 2010 Feb 2. J Clin Immunol. 2010. PMID: 20127275 Free PMC article. Review.
-
Normal mouse kidneys contain activated and CD3+CD4- CD8- double-negative T lymphocytes with a distinct TCR repertoire.J Leukoc Biol. 2008 Dec;84(6):1400-9. doi: 10.1189/jlb.0907651. Epub 2008 Sep 2. J Leukoc Biol. 2008. PMID: 18765477 Free PMC article.
-
Robust genital gag-specific CD8+ T-cell responses in mice upon intramuscular immunization with simian adenoviral vectors expressing HIV-1-gag.Eur J Immunol. 2010 Dec;40(12):3426-38. doi: 10.1002/eji.201040440. Epub 2010 Nov 11. Eur J Immunol. 2010. PMID: 21108465 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources