April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Defining The HSV-Specific CD8+ T Cell Repertoire In C57BL/6 Mice
Author Affiliations & Notes
  • Robert L. Hendricks
    Ophthalmology, Univ of Pittsburgh Eye & Ear Inst, Pittsburgh, Pennsylvania
  • Anthony St. Leger
    Ophthalmology, Univ of Pittsburgh Eye & Ear Inst, Pittsburgh, Pennsylvania
  • Bjoern Peters
    Center for Infectious Disease, La Jolla Institute for Allergy & Immunology, La Jolla, California
  • John Sidney
    Center for Infectious Disease, La Jolla Institute for Allergy & Immunology, La Jolla, California
  • Alessandro Sette
    Center for Infectious Disease, La Jolla Institute for Allergy & Immunology, La Jolla, California
  • Footnotes
    Commercial Relationships  Robert L. Hendricks, None; Anthony St. Leger, None; Bjoern Peters, None; John Sidney, None; Alessandro Sette, None
  • Footnotes
    Support  NIH EY05945, NIH P30-EY08099, Research to Prevent Blindness, Inc. and the Eye and Ear Foundation of Pittsburgh
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 4369. doi:https://doi.org/
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      Robert L. Hendricks, Anthony St. Leger, Bjoern Peters, John Sidney, Alessandro Sette; Defining The HSV-Specific CD8+ T Cell Repertoire In C57BL/6 Mice. Invest. Ophthalmol. Vis. Sci. 2011;52(14):4369. doi: https://doi.org/.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Herpes simplex virus type 1 (HSV-1) glycoprotein B (gB) contains a strongly immunodominant CD8+ T cell eptiope (gB498-505) that is recognized by 50% of both the CD8+ effector T cells in acutely infected trigeminal ganglia (TG) and the CD8+ memory T cells in latently infected TG of C57BL/6 mice. The goal of this study was to identify the subdominant epitopes recognized by 50% of the HSV-specific CD8+ T cell repertoire.

Methods: : The entire HSV-1 proteome (GI 9629378) was scanned for peptide sequences predicted to have a high affinity binding capacity for the MHC class I molecules H-2 Kb or H-2 Db. For each MHC allele, the 188 peptides with the highest median ranks, corresponding to the top 0.5% scoring peptides, were selected for screening. B6WT3 fibroblast targets were pulsed with peptide and used to stimulate dispersed TG or spleen cells obtained 8 days after HSV-1 corneal infection. Responding CD8+ T cells were quantified by intracellular staining for IFN-γ and TNF-α followed by flow cytometry analysis.

Results: : Of 376 predicted HSV-1 CD8+ T cell epitopes, 19 (gB498-505 and 18 subdominant epitopes) stimulated CD8+ T cells in the spleens and TG of HSV-1 acutely infected mice. These 19 epitopes identified virtually all CD8+ T cells in the infected TG and represented all or the vast majority of the HSV-specific CD8+ TCR repertoire. A similar frequency of epitope specific CD8+ T cells was observed in the TG and among HSV-specific CD8+ T cells in the spleen. Only 11 of approximately 84 HSV-1 proteins are recognized by CD8+ T cells and most (~80%) are expressed before viral DNA synthesis. Neither the immunodominance of gB498-505 nor the dominance hierarchy of the subdominant epitopes is due solely to MHC or TCR affinity.

Conclusions: : We conclude that the vast majority of CD8+ T cells in HSV-1 acutely infected TG are HSV-specific, that HSV-1 β and γ1 proteins that are expressed before viral DNA synthesis are favored targets of CD8+ T cells, and that dominance within the TCR repertoire is likely due to the frequency or expansion and survival characteristics of CD8+ T cell precursors.

Keywords: herpes simplex virus • cytokines/chemokines • immunomodulation/immunoregulation 
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