Cross-Clade Cytotoxic T Cell Response to Human Immunodeficiency Virus Type 1 Proteins among HLA Disparate North Americans and Thais
A globally effective vaccine will need to elicit cytotoxic T lymphocytes (CTL) capable of recognizing diverse human immunodeficiency virus type 1 (HIV-1) clades. Study of the cellular immune responses of HIV-1—infected persons may allow predictions to be made regarding useful vaccine antigen compone...
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Published in | The Journal of infectious diseases Vol. 178; no. 4; pp. 1040 - 1046 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
01.10.1998
University of Chicago Press |
Subjects | |
Online Access | Get full text |
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Summary: | A globally effective vaccine will need to elicit cytotoxic T lymphocytes (CTL) capable of recognizing diverse human immunodeficiency virus type 1 (HIV-1) clades. Study of the cellular immune responses of HIV-1—infected persons may allow predictions to be made regarding useful vaccine antigen components. The frequency and magnitude of CTL responses to clade E and B Gag, Pol-RT, Env, and Nef proteins were compared in 12 HLA-characterized, clade E—infected Thais and in 10 clade B—infected North Americans using vaccinia recombinant constructs for protein expression. While responses were detected against all proteins, they were most frequent and cross-reactive to Gag in both groups. Pol-RT was recognized less frequently in Thais than North Americans. Cross-clade protein recognition was common but not uniformly present among these HLA-disparate individuals. Population-specific CTL data are needed to adequately prepare for vaccine trials outside of North America and Europe. |
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Bibliography: | ark:/67375/HXZ-5HS2HZ3K-P Presented in part: Fourth International Congress on AIDS in Asia and the Pacific, Manila, Philippines, October 1997 (abstract B-061-081). istex:D99B6A2ED58983AFADAC77B088EF2E73375E1E16 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1086/515652 |