Evidence for selective accumulation of intrathyroidal T lymphocytes in human autoimmune thyroid disease based on T cell receptor V gene usage
- PMID: 1530851
- PMCID: PMC442831
- DOI: 10.1172/JCI115556
Evidence for selective accumulation of intrathyroidal T lymphocytes in human autoimmune thyroid disease based on T cell receptor V gene usage
Abstract
We have investigated the T cell receptor V alpha and V beta gene family usage by T lymphocytes infiltrating affected thyroids in patients with autoimmune thyroid disease. We show that the intrathyroidal T lymphocytes from patients (n = 6) with autoimmune thyroid disease display a widespread usage of V beta gene families with an average of 14.4/19 V beta gene families similar to the peripheral T lymphocytes of the same patients. Because we recently reported that the utilization of V alpha gene families is markedly reduced within these mitogen-stimulated intrathyroidal T cell populations, as well as within intact tissue from similar patients (n = 4) (overall mean of 4.0/18 families detected), these results indicate that in thyroids of patients with autoimmune thyroid disease the lymphocytes are selectively accumulating based on their V alpha rather than V beta elements. This preferential hTcR V alpha and widespread V beta gene usage was not mimicked in most 7-d autologous mixed lymphocyte reactions using non-T cell stimulators (n = 6) or EB-virus immortalized autologous B cell lines (n = 3). Hence, the selective V gene utilization by intrathyroidal T cells is likely to be secondary to multiepitopic thyroidal autoantigens activating thyroid infiltrating T cells or to the presence of a superantigenlike thyroidal self-antigen, capable of determining a selective infiltration or activation of a variety of T lymphocytes on the basis of their V alpha gene usage.
Similar articles
-
[Antigen receptor V beta gene usage of T lymphocytes in diseased thyroids in patients with autoimmune thyroid diseases].Zhonghua Bing Li Xue Za Zhi. 2001 Aug;30(4):268-72. Zhonghua Bing Li Xue Za Zhi. 2001. PMID: 11758215 Chinese.
-
Evidence of limited variability of antigen receptors on intrathyroidal T cells in autoimmune thyroid disease.N Engl J Med. 1991 Jul 25;325(4):238-44. doi: 10.1056/NEJM199107253250404. N Engl J Med. 1991. PMID: 1829139
-
Evidence for selective accumulation of V beta 8+ T lymphocytes in experimental autoimmune uveoretinitis induced with two different retinal antigens.J Immunol. 1993 Aug 1;151(3):1627-36. J Immunol. 1993. PMID: 8393049
-
Preferential use of T-cell receptor V genes in human autoimmune thyroid disease.Autoimmunity. 1992;13(1):11-6. doi: 10.3109/08916939209014630. Autoimmunity. 1992. PMID: 1420802 Review.
-
T-cell receptors and autoimmune thyroid disease--signposts for T-cell-antigen driven diseases.Int Rev Immunol. 1999;18(1-2):111-40. doi: 10.3109/08830189909043021. Int Rev Immunol. 1999. PMID: 10614741 Review.
Cited by
-
Tumour infiltrating T-cells in gastric lymphoma.Virchows Arch. 1995;426(1):1-2. doi: 10.1007/BF00194691. Virchows Arch. 1995. PMID: 7704318 No abstract available.
-
SARS-CoV-2 plays a pivotal role in inducing hyperthyroidism of Graves' disease.Endocrine. 2021 Aug;73(2):243-254. doi: 10.1007/s12020-021-02770-6. Epub 2021 Jun 9. Endocrine. 2021. PMID: 34106438 Free PMC article. Review.
-
Analysis of T cell receptor Vbeta diversity in peripheral CD4 and CD8 T lymphocytes in patients with autoimmune thyroid diseases.Clin Exp Immunol. 2009 Feb;155(2):166-72. doi: 10.1111/j.1365-2249.2008.03842.x. Epub 2008 Nov 25. Clin Exp Immunol. 2009. PMID: 19040601 Free PMC article.
-
The human T cell receptor V beta repertoire of normal peripheral blood lymphocytes before and after mitogen stimulation.Clin Exp Immunol. 1993 May;92(2):361-6. doi: 10.1111/j.1365-2249.1993.tb03405.x. Clin Exp Immunol. 1993. PMID: 8387412 Free PMC article.
-
In search of TCR restriction in autoreactive T cell in human autoimmunity: why is it so elusive?Clin Exp Immunol. 1993 Feb;91(2):189-92. doi: 10.1111/j.1365-2249.1993.tb05880.x. Clin Exp Immunol. 1993. PMID: 8428385 Free PMC article. No abstract available.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical