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PMID: 11709777 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Strong HLA class I--restricted T cell responses in dengue hemorrhagic fever: a double-edged sword?

The Journal of infectious diseases ·Vol. 184 ·No. 11 ·2001-12-01 ·Pages 1369-73

Loke H, Bethell DB, Phuong CX, Dung M, Schneider J, White NJ, Day NP, Farrar J, Hill AV

Abstract

Dengue is an increasingly important cause of morbidity and mortality in the tropics, but vaccine development has been impeded by a poor understanding of disease pathogenesis and, in particular, of immunologic enhancement. In a large case-control study of Vietnamese patients with dengue hemorrhagic fever (DHF), variation at the HLA-A locus was significantly associated with susceptibility to DHF (P=.02), and specific HLA-A susceptibility and resistance alleles were identified. HLA-A-specific epitopes were predicted from binding motifs, and ELISPOT analyses of patients with DHF revealed high frequencies of circulating CD8 T lymphocytes that recognized both serotype-specific and -cross-reactive dengue virus epitopes. Thus, strong CD8 T cell responses are induced by natural dengue virus infection, and HLA class I genetic variation is a risk factor for DHF. These genetic and immunologic data support both protective and pathogenic roles for dengue virus-specific CD8 T cell responses in severe disease. The potentially pathogenic role of serotype-cross-reactive CD8 T cells poses yet another obstacle to successful dengue vaccine development.

MeSH Terms
Adolescent Adult Antigens, Viral/immunology CD8-Positive T-Lymphocytes/immunology Case-Control Studies Cells, Cultured Child Child, Preschool Dengue Virus/immunology Epitopes/immunology Female Genetic Predisposition to Disease Genetic Variation HLA-A Antigens/genetics Humans Interferon-gamma/biosynthesis Lymphocyte Activation Major Histocompatibility Complex Male Polymorphism, Genetic Severe Dengue/genetics,immunology
Chemicals
Antigens, Viral Epitopes HLA-A Antigens Interferon-gamma
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Loke H
Nuffield Department of Medicine, John Radcliffe Hospital and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom. hsin.loke@pwcglobal.com
Bethell D B
Phuong C X
Dung M
Schneider J
White N J
Day N P
Farrar J
Hill A V
Article Info
Journal
The Journal of infectious diseases
Abbr.
J Infect Dis
ISSN
0022-1899
Published
2001-12-01
Epub
2001-00-13
Pages
1369-73
Language
English
Region
United States
NLM ID
0413675
Subset
IM
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