Abstract
The effect of herpes simplex virus type 1 (HSV-1) infection on human cytotoxic T-lymphocyte (CTL) lytic function was assessed. All HSV-infected CTL populations tested were significantly inhibited in lysing target cells. The inhibition of CTL lytic function by infection with HSV-1 was independent of T-cell receptor-mediated antigen recognition and did not involve virus-induced shutoff of host protein synthesis, the expression of the HSV-1 transactivation protein, ICP4, or replicating virus. Understanding the functional impairment of CTL following infection with HSV may have important implications for HSV-induced immunosuppression and the mechanism of HSV persistence in immunocompetent hosts.
MeSH Terms
Cytotoxicity, Immunologic
Herpes Simplex/immunology,microbiology
Herpesvirus 1, Human/genetics,immunology,pathogenicity
Humans
Immediate-Early Proteins/immunology
In Vitro Techniques
Isoantigens
Lymphocyte Culture Test, Mixed
Mutation
T-Lymphocytes, Cytotoxic/immunology,microbiology
Tumor Cells, Cultured/immunology
Chemicals
Immediate-Early Proteins
Isoantigens
herpes simplex virus, type 1 protein ICP4
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Posavad C M
Department of Pathology, McMaster University Health Sciences Centre, Hamilton, Ontario, Canada.
Newton J J
Rosenthal K L
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