Endogenous antigen presentation impacts on T-box transcription factor expression and functional maturation of CD8+ T cells - PubMed (original) (raw)

. 2012 Oct 18;120(16):3237-45.

doi: 10.1182/blood-2012-03-420182. Epub 2012 Aug 31.

Diah Elhassen, Stephanie Gras, Katherine K Wynn, Vijayendra Dasari, Judy Tellam, Siok-Keen Tey, Sweera Rehan, Yu Chih Liu, Jamie Rossjohn, Scott R Burrows, Rajiv Khanna

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Endogenous antigen presentation impacts on T-box transcription factor expression and functional maturation of CD8+ T cells

Corey Smith et al. Blood. 2012.

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Abstract

T-box transcription factors T-bet (Tbx21) and Eomesodermin (Eomes) are critical players in CD8(+) cytotoxic T lymphocyte effector function and differentiation, but how the expression of these transcription factors is regulated remains poorly defined. Here we show that dominant T cells directed toward human CMV, expressing significantly higher levels of T-bet with graded loss of Eomes expression (T-bet(hi)Eomes(hi/lo)), are more efficient in recognizing endogenously processed peptide-major histocompatibility complexes (pMHC) compared with subdominant virus-specific T cells expressing lower levels of T-bet and high levels of Eomes (T-bet(int)Eomes(hi)). Paradoxically, the T-bet(hi)Eomes(hi/lo) dominant populations that efficiently recognized endogenous antigen demonstrated lower intrinsic avidity for pMHC, whereas T-bet(int)Eomes(hi) subdominant populations were characterized by higher pMHC avidity and less efficient recognition of virus-infected cells. Importantly, differential endogenous viral antigen recognition by CMV-specific CD8(+) T cells also correlated with the differentiation status and expression of perforin, granzyme B and K. Furthermore, we demonstrate that the expression of T-bet correlates with clonal expansion, differentiation status, and expression of perforin, granzyme B and K in antigen-specific T cells. These findings illustrate how endogenous viral antigen presentation during persistent viral infection may influence the transcriptional program of virus-specific T cells and their functional profile in the peripheral blood of humans.

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