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Molecular heterogeneity of a Graves’ thyroid-infiltrating T cell population rich in CD8+ and γδ+ T cells

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Abstract

We report here on the isolation and repertoire characterization of a Graves’ thyroid T cell population which, unlike most Graves’ thyroid T cell isolates reported before, was rich in CD4-CD8-T cells (16%, all TcRγδ+) and CD8+ T cells (75%) [TcRαβ+ (59%) and TcRγδ+ (16%)]. Only 7% of the isolated T cells were CD4+. By contrast, <2% of peripheral blood mononuclear cells from the same patient were γδ+ and <14% were CD8+. Sequence analysis of 18 TcRδ cDNAs prepared from these cells indicated the presence of at least 17 different γδ+ T cell clonotypes with molecularly heterogeneous antigen-binding site sequences. As opposed to most peripheral blood γδ+ T cells (express Vδ2 TcRs), 13 of the 17 different TcRδ clonotypes used a Vδ1 gene, although PCR amplification of TcRγ- and TcRδ-specific cDNAs with Vδ- and Vγ-gene family-specific oligonucleotides confirmed usage of all 4 Vγ and all 6 Vδ families. Sequence analysis of 21 TcRα cDNAs from a TcRα-specific cDNA library indicated the presence of at least 12 different clonotypes, using 8 different Vα gene families and heterogeneous antigen-binding site sequences. These results are in contrast with the selective Vα gene usage reported for other intrathyroidal T cell subpopulations in autoimmune thyroid disease.

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Santamaria, P., Lewis, C. & Barbosa, J.J. Molecular heterogeneity of a Graves’ thyroid-infiltrating T cell population rich in CD8+ and γδ+ T cells. J Endocrinol Invest 16, 913–920 (1993). https://doi.org/10.1007/BF03348958

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