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PMID: 1707922 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Class I MHC-restricted cytotoxic T lymphocyte recognition of cells infected with human cytomegalovirus does not require endogenous viral gene expression.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 146 ·No. 8 ·1991-04-15 ·Pages 2795-804

Riddell SR, Rabin M, Geballe AP, Britt WJ, Greenberg PD

Abstract

The human pathogen CMV, is a major cause of morbidity and mortality in immunocompromised hosts. The CD8+ class I-restricted CTL response to CMV assists in preventing progression of CMV infection to life-threatening disease; however, the viral Ag recognized by CD8+ CTL are not well characterized. In general, virus-specific CTL recognize endogenously synthesized viral proteins processed and presented associated with class I MHC molecules. Although proteins or inactivated virions have been experimentally delivered to the cytoplasm to result in class I MHC presentation, this mode of Ag delivery to the class I processing pathway after natural viral entry has not been documented in humans. Our data demonstrate that the CMV-specific class I-restricted CTL response in individuals latently infected with CMV is predominantly specific for selected structural virion proteins introduced into the cell after viral penetration and efficient recognition occurs in the absence of de novo viral gene expression. This CTL response may provide a biological advantage for limiting the spread of infection after CMV reactivation because infected cells are lysed before viral assembly.

MeSH Terms
Antigens, Viral/biosynthesis,immunology Blotting, Northern Cytomegalovirus/immunology Cytomegalovirus Infections/immunology Cytotoxicity, Immunologic Epitopes Gene Expression Genes, Viral/physiology Histocompatibility Antigens Class I/immunology Humans Immediate-Early Proteins RNA, Messenger/analysis T-Lymphocytes, Cytotoxic/immunology
Chemicals
Antigens, Viral Epitopes Histocompatibility Antigens Class I Immediate-Early Proteins RNA, Messenger immediate-early proteins, cytomegalovirus
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Riddell S R
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Rabin M
Geballe A P
Britt W J
Greenberg P D
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1991-04-15
Pages
2795-804
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI26672 · United States
NIAID NIH HHS · AI27291 · United States
NCI NIH HHS · CA18029 · United States
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