↓ Skip to main content

PLOS

Vaccine-Induced IgG Antibodies to V1V2 Regions of Multiple HIV-1 Subtypes Correlate with Decreased Risk of HIV-1 Infection

Overview of attention for article published in PLOS ONE, February 2014
Altmetric Badge

Mentioned by

twitter
6 X users
patent
1 patent

Citations

dimensions_citation
243 Dimensions

Readers on

mendeley
124 Mendeley
citeulike
1 CiteULike
Title
Vaccine-Induced IgG Antibodies to V1V2 Regions of Multiple HIV-1 Subtypes Correlate with Decreased Risk of HIV-1 Infection
Published in
PLOS ONE, February 2014
DOI 10.1371/journal.pone.0087572
Pubmed ID
Authors

Susan Zolla-Pazner, Allan deCamp, Peter B. Gilbert, Constance Williams, Nicole L. Yates, William T. Williams, Robert Howington, Youyi Fong, Daryl E. Morris, Kelly A. Soderberg, Carmela Irene, Charles Reichman, Abraham Pinter, Robert Parks, Punnee Pitisuttithum, Jaranit Kaewkungwal, Supachai Rerks-Ngarm, Sorachai Nitayaphan, Charla Andrews, Robert J. O’Connell, Zhi-yong Yang, Gary J. Nabel, Jerome H. Kim, Nelson L. Michael, David C. Montefiori, Hua-Xin Liao, Barton F. Haynes, Georgia D. Tomaras

Abstract

In the RV144 HIV-1 vaccine efficacy trial, IgG antibody (Ab) binding levels to variable regions 1 and 2 (V1V2) of the HIV-1 envelope glycoprotein gp120 were an inverse correlate of risk of HIV-1 infection. To determine if V1V2-specific Abs cross-react with V1V2 from different HIV-1 subtypes, if the nature of the V1V2 antigen used to asses cross-reactivity influenced infection risk, and to identify immune assays for upcoming HIV-1 vaccine efficacy trials, new V1V2-scaffold antigens were designed and tested. Protein scaffold antigens carrying the V1V2 regions from HIV-1 subtypes A, B, C, D or CRF01_AE were assayed in pilot studies, and six were selected to assess cross-reactive Abs in the plasma from the original RV144 case-control cohort (41 infected vaccinees, 205 frequency-matched uninfected vaccinees, and 40 placebo recipients) using ELISA and a binding Ab multiplex assay. IgG levels to these antigens were assessed as correlates of risk in vaccine recipients using weighted logistic regression models. Levels of Abs reactive with subtype A, B, C and CRF01_AE V1V2-scaffold antigens were all significant inverse correlates of risk (p-values of 0.0008-0.05; estimated odds ratios of 0.53-0.68 per 1 standard deviation increase). Thus, levels of vaccine-induced IgG Abs recognizing V1V2 regions from multiple HIV-1 subtypes, and presented on different scaffolds, constitute inverse correlates of risk for HIV-1 infection in the RV144 vaccine trial. The V1V2 antigens provide a link between RV144 and upcoming HIV-1 vaccine trials, and identify reagents and methods for evaluating V1V2 Abs as possible correlates of protection against HIV-1 infection.

X Demographics

X Demographics

The data shown below were collected from the profiles of 6 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 124 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 <1%
United States 1 <1%
Unknown 122 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 38 31%
Researcher 18 15%
Student > Master 12 10%
Student > Bachelor 10 8%
Student > Postgraduate 8 6%
Other 15 12%
Unknown 23 19%
Readers by discipline Count As %
Agricultural and Biological Sciences 29 23%
Medicine and Dentistry 20 16%
Biochemistry, Genetics and Molecular Biology 18 15%
Immunology and Microbiology 16 13%
Nursing and Health Professions 4 3%
Other 10 8%
Unknown 27 22%