4.6 Article

Diversity in CD8+ T Cell Function and Epitope Breadth Among Persons with Genital Herpes

Journal

JOURNAL OF CLINICAL IMMUNOLOGY
Volume 30, Issue 5, Pages 703-722

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10875-010-9441-2

Keywords

HSV-2; T cells; antigens/peptides/epitopes; virus

Categories

Funding

  1. [NIH P01-AI030731]
  2. [NIH P30 AI207757]
  3. [NIH AI 50132]
  4. [NIH R37-AI042528]

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CD8(+) T cells are known to be important in clearing herpes simplex virus (HSV) infections. However, investigating the specific antiviral mechanisms employed by HSV-2-specific T cell populations is limited by a lack of reagents such as CD8(+) T cell epitopes and specific tetramers. Using a combination of intracellular cytokine staining flow cytometry and ELISpot methods, we functionally characterized peripheral HSV-2-specific CD8(+) T cells from peripheral blood mononuclear cell (PBMC) that recognize 14 selected HSV-2 open-reading frames (ORFs) from 55 HSV-2 seropositive persons; within these ORFs, we subsequently identified more than 20 unique CD8(+) T cell epitopes. CD8(+) T cells to HSV-2 exhibited significant heterogeneity in their functional characteristics, proliferation, production of inflammatory cytokines, and potential to degranulate ex vivo. The diversity in T cell response in these ex vivo assessments offers the potential of defining immune correlates of HSV-2 reactivation in humans.

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