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Publication : Phenotypic and Functional Signatures of Herpes Simplex Virus-Specific Effector Memory CD73<sup>+</sup>CD45RA<sup>high</sup>CCR7<sup>low</sup>CD8<sup>+</sup> T<sub>EMRA</sub> and CD73<sup>+</sup>CD45RA<sup>low</sup>CCR7<sup>low</sup>CD8<sup>+</sup> T<sub>EM</sub> Cells Are Associated with Asymptomatic Ocular Herpes.

First Author  Srivastava R Year  2018
Journal  J Immunol Volume  201
Issue  8 Pages  2315-2330
PubMed ID  30201808 Mgi Jnum  J:266197
Mgi Id  MGI:6203270 Doi  10.4049/jimmunol.1800725
Citation  Srivastava R, et al. (2018) Phenotypic and Functional Signatures of Herpes Simplex Virus-Specific Effector Memory CD73(+)CD45RA(high)CCR7(low)CD8(+) TEMRA and CD73(+)CD45RA(low)CCR7(low)CD8(+) TEM Cells Are Associated with Asymptomatic Ocular Herpes. J Immunol 201(8):2315-2330
abstractText  HSV type 1 (HSV-1)-specific CD8(+) T cells protect from herpes infection and disease. However, the nature of protective CD8(+) T cells in HSV-1 seropositive healthy asymptomatic (ASYMP) individuals (with no history of clinical herpes disease) remains to be determined. In this study, we compared the phenotype and function of HSV-specific CD8(+) T cells from HLA-A*02:01-positive ASYMP and symptomatic (SYMP) individuals (with a documented history of numerous episodes of recurrent ocular herpetic disease). We report that although SYMP and ASYMP individuals have similar frequencies of HSV-specific CD8(+) T cells, the "naturally" protected ASYMP individuals have a significantly higher proportion of multifunctional HSV-specific effector memory CD8(+) T cells (CD73(+)CD45RA(high)CCR7(low)CD8(+) effector memory RA (TEMRA) and CD73(+)CD45RA(low)CCR7(low)CD8(+) effector memory (TEM) as compared with SYMP individuals. Similar to humans, HSV-1-infected ASYMP B6 mice had frequent multifunctional HSV-specific CD73(+)CD8(+) T cells in the cornea, as compared with SYMP mice. Moreover, in contrast to wild type B6, CD73(-/-) deficient mice infected ocularly with HSV-1 developed more recurrent corneal herpetic infection and disease. This was associated with less functional CD8(+) T cells in the cornea and trigeminal ganglia, the sites of acute and latent infection. The phenotypic and functional characteristics of HSV-specific circulating and in situ CD73(+)CD8(+) T cells, demonstrated in both ASYMP humans and mice, suggest a positive role for effector memory CD8(+) T cells expressing the CD73 costimulatory molecule in the protection against ocular herpes infection and disease. These findings are important for the development of safe and effective T cell-based herpes immunotherapy.
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