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PMID: 1705990 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Dengue virus-specific, human CD4+ CD8- cytotoxic T-cell clones: multiple patterns of virus cross-reactivity recognized by NS3-specific T-cell clones.

Journal of virology ·Vol. 65 ·No. 4 ·1991-04-00 ·Pages 1823-8

Kurane I, Brinton MA, Samson AL, Ennis FA

Abstract

Thirteen dengue virus-specific, cytotoxic CD4+ CD8- T-cell clones were established from a donor who was infected with dengue virus type 3. These clones were examined for virus specificity and human leukocyte antigen (HLA) restriction in cytotoxic assays. Six patterns of virus specificities were determined. Two serotype-specific clones recognized only dengue virus type 3. Two dengue virus subcomplex-specific clones recognized dengue virus types 2, 3, and 4, and one subcomplex-specific clone recognized dengue virus types 1, 2, and 3. Four dengue virus serotype-cross-reactive clones recognized dengue virus types 1, 2, 3, and 4. One flavivirus-cross-reactive clone recognized dengue virus types 1, 2, 3, and 4 and West Nile virus (WNV), but did not recognize yellow fever virus (YFV), whereas three flavivirus-cross-reactive clones recognized dengue virus types 1, 2, 3, and 4, WNV, and YFV. HLA restriction in the lysis by these T-cell clones was also heterogeneous. HLA-DP, HLA-DQ, and HLA-DR were used as restriction elements by various T-cell clones. We also examined the recognition of viral nonstructural protein NS3, purified from cells infected with dengue virus type 3 or WNV, by these T-cell clones. One serotype-specific clone, two dengue virus subcomplex-specific clones, and three dengue virus serotype-cross-reactive clones recognized NS3 of dengue virus type 3. One flavivirus-cross-reactive clone recognized NS3 of dengue virus type 3 and WNV. These results indicate that heterogeneous dengue virus-specific CD4+ cytotoxic T cells are stimulated in response to infection with a dengue virus and that a nonstructural protein, NS3, contains multiple dominant T-cell epitopes.

MeSH Terms
Animals CD4-Positive T-Lymphocytes/immunology,microbiology Cells, Cultured Clone Cells/immunology,microbiology Cross Reactions Cytotoxicity, Immunologic Dengue/immunology Dengue Virus/immunology Epitopes HLA Antigens/immunology Humans RNA Helicases RNA Nucleotidyltransferases/immunology Sensitivity and Specificity Serine Endopeptidases T-Lymphocytes, Cytotoxic/immunology Viral Nonstructural Proteins Viral Proteins/immunology
Chemicals
Epitopes HLA Antigens NS3 protein, flavivirus Viral Nonstructural Proteins Viral Proteins RNA Nucleotidyltransferases Serine Endopeptidases RNA Helicases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kurane I
Department of Medicine, University of Massachusetts Medical Center, Worcester 01655.
Brinton M A
Samson A L
Ennis F A
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1991-04-00
Pages
1823-8
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC239991
Subset
IM
Grants
NIAID NIH HHS · T32-AI07272 · United States
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