Abstract |
The results of the RV144 vaccine clinical trial showed a correlation between high level of anti-V1V2 antibodies (Abs) and a decreased risk of acquiring HIV-1 infection. This turned the focus of HIV vaccine design to the induction of elevated levels of anti-V2 Abs to increase vaccine efficacy. In plasma samples from HIV-1 infected Cameroonian individuals, we observed broad variations in levels of anti-V2 Abs, and 6 of the 79 plasma samples tested longitudinally displayed substantial deficiency of V2 Abs. Sequence analysis of the V2 region from plasma viruses and multivariate analyses of V2 characteristics showed a significant difference in several features between V2-deficient and V2-reactive plasma Abs. These results suggest that HIV vaccine immunogens containing a shorter V2 region with fewer glycosylation sites and higher electrostatic charges can be beneficial for induction of a higher level of anti-V2 Abs and thus contribute to HIV vaccine efficacy.
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Authors | Lily Liu, Liuzhe Li, Aubin Nanfack, Luzia M Mayr, Sonal Soni, Adam Kohutnicki, Lucy Agyingi, Xiao-Hong Wang, Michael Tuen, Yongzhao Shao, Maxim Totrov, Susan Zolla-Pazner, Xian-Peng Kong, Ralf Duerr, Miroslaw K Gorny |
Journal | Virology
(Virology)
Vol. 529
Pg. 57-64
(03 2019)
ISSN: 1096-0341 [Electronic] United States |
PMID | 30665098
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Copyright | Copyright © 2019 Elsevier Inc. All rights reserved. |
Chemical References |
- AIDS Vaccines
- HIV Antibodies
- HIV Antigens
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Topics |
- AIDS Vaccines
(immunology)
- Cameroon
(epidemiology)
- HIV Antibodies
(blood, immunology)
- HIV Antigens
(immunology)
- HIV Infections
(epidemiology, immunology, prevention & control, virology)
- HIV-1
- Humans
- Multivariate Analysis
- Viral Load
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