Restricted T Cell Receptor β‐Chain Variable Region Protein Use by Cornea‐Derived CD4+and CD8+Herpes Simplex Virus–Specific T Cells in Patients with Herpetic Stromal Keratitis
Author(s) -
Jeroen Maertzdorf,
Georges M. G. M. Verjans,
Lies Remeijer,
Alexander van der Kooi,
Albert D. M. E. Osterhaus
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/367991
Subject(s) - cytotoxic t cell , herpes simplex virus , cd8 , t cell , biology , cornea , stromal cell , virology , t lymphocyte , immunology , flow cytometry , microbiology and biotechnology , virus , antigen , in vitro , cancer research , immune system , genetics , neuroscience
Herpetic stromal keratitis (HSK) is a T helper type 1 cell-mediated inflammatory disease triggered by herpes simplex virus (HSV) infection of the cornea. In contrast to animal models of HSK, little is known about the role of T cells in human HSK. The phenotypes and repertoires of HSV-specific T cells recovered from the corneas of 12 patients with HSK were determined by flow cytometry. Cornea-derived T cell lines (TCLs) from 10 of the 12 patients contained high numbers of HSV-specific T cells. HSV reactivity was HSV type common and involved relatively more CD8(+) than CD4(+) T cells. The majority of the TCLs showed restricted T cell receptor beta-chain variable region protein (TCRBV) use. T cells expressing 1 or 2 TCRBVs dominated the HSV-1 reactivity in 3 of 5 TCLs analyzed. The data demonstrate that both CD4(+) and CD8(+) T cells may be involved in the HSV-specific T cell response in the corneas of patients with HSK and suggest that restricted TCRBV use by cornea-residing HSV-specific T cells occurs.
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