1. Herpes virus entry mediator (HVEM) modulates proliferation and activation of regulatory T cells following HSV-1 infection.
- Author
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Sharma, Shalini, Rajasagi, Naveen K., Veiga-Parga, Tamara, and Rouse, Barry T.
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HERPES simplex virus , *T cells , *CELL proliferation , *CELLULAR control mechanisms , *HERPESVIRUS diseases , *CD4 antigen - Abstract
In many infections, especially those that are chronic such as Herpes Simplex Virus-1 (HSV-1), the outcome may be influenced by the activity of one or more types of regulatory T cells (Tregs). Some infections can cause Treg expansion, but how viruses might promote preferential Treg expansion is has been unclear. In this report, we demonstrate a possible mechanism by which HSV (Herpes Simplex virus-1) infection could act to signal and expands the Treg population. We show that CD4 + FoxP3 + Tregs up- regulate HVEM (herpes virus entry mediator), which is a binding site for major viral glycoprotein HSVgD, following HSV infection, which is a binding site for major viral glycoprotein HSVgD. Recombinant HSVgD enhanced the proliferation of CD4 + FoxP3 + Tregs cells in-vitro. Furthermore, compared to wild type (WT), HVEM deficient mice (HVEM−/−) generated a weaker Treg responses represented by significantly diminished ratios of CD4 + FoxP3 + /CD4 + FoxP3 - cells along with diminished proportions of FoxP3 + Tregscells co-expressing Treg activation markers and a reduced MFI of FoxP3 expression on CD4 + T cells. Consistent with defective Treg responses, HVEM−/− animals were more susceptible to HSV-1 induced ocular immunopathology, with more severe lesions in HVEM−/− animals. Our results indicate that HVEM regulates Treg responses, and its modulation could represent a useful approach to control HSV induced corneal immunopathology. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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