Escape from Autologous Neutralizing Antibodies in Acute/Early Subtype C HIV-1 Infection Requires Multiple Pathways
Abstract
One aim for an HIV vaccine is to elicit neutralizing antibodies (Nab) that can limit replication of genetically diverse viruses and prevent establishment of a new infection. Thus, identifying the strengths and weaknesses of Nab during the early stages of natural infection could prove useful in achieving this goal. Here we demonstrate that viral escape readily occurred despite the development of high titer autologous Nab in two subjects with acute/early subtype C infection. To provide a detailed portrayal of the escape pathways, Nab resistant variants identified at multiple time points were used to create a series of envelope (Env) glycoprotein chimeras and mutants within the background of a corresponding newly transmitted Env. In one subject, Nab escape was driven predominantly by changes in the region of gp120 that extends from the beginning of the V3 domain to the end of the V5 domain (V3V5). However, Nab escape pathways in this subject oscillated and at times required cooperation between V1V2 and the gp41 ectodomain. In the second subject, escape was driven by changes in V1V2. This V1V2-dependent escape pathway was retained over time, and its utility was reflected in the virus’s ability to escape from two distinct monoclonal antibodies (Mabs) derivedmore »
- Authors:
-
- Emory University, Atlanta, GA (United States)
- Zambia Emory HIV Research Project, ZEHRP, Lusaka (Zambia); Zambia Blood Transfusion Service, Lusaka (Zambia)
- Zambia Emory HIV Research Project, ZEHRP, Lusaka (Zambia); Emory University, Atlanta, GA (United States)
- Public Health Research Institute., Newark, NJ (United States); University of Medicine and Dentistry, Newark, NJ (United States)
- University of Alabama, Birmingham, AL (United States)
- Tulane University, New Orleans, LA (United States)
- Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
- Publication Date:
- Research Org.:
- Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Biological and Environmental Research (BER); National Institutes of Health (NIH); Bill and Melinda Gates Foundation
- OSTI Identifier:
- 1627894
- Grant/Contract Number:
- AC52-06NA25396; R01-AI58706; R01-AI51231; U01-AI78410; 37874; 38619
- Resource Type:
- Accepted Manuscript
- Journal Name:
- PLoS Pathogens
- Additional Journal Information:
- Journal Volume: 5; Journal Issue: 9; Journal ID: ISSN 1553-7374
- Publisher:
- Public Library of Science
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES; HIV-1; glycosylation; hybridomas; protein sequencing; B cells; cloning; DNA cloning; polymerase chain reaction
Citation Formats
Rong, Rong, Li, Bing, Lynch, Rebecca M., Haaland, Richard E., Murphy, Megan K., Mulenga, Joseph, Allen, Susan A., Pinter, Abraham, Shaw, George M., Hunter, Eric, Robinson, James E., Gnanakaran, S., and Derdeyn, Cynthia A. Escape from Autologous Neutralizing Antibodies in Acute/Early Subtype C HIV-1 Infection Requires Multiple Pathways. United States: N. p., 2009.
Web. doi:10.1371/journal.ppat.1000594.
Rong, Rong, Li, Bing, Lynch, Rebecca M., Haaland, Richard E., Murphy, Megan K., Mulenga, Joseph, Allen, Susan A., Pinter, Abraham, Shaw, George M., Hunter, Eric, Robinson, James E., Gnanakaran, S., & Derdeyn, Cynthia A. Escape from Autologous Neutralizing Antibodies in Acute/Early Subtype C HIV-1 Infection Requires Multiple Pathways. United States. https://doi.org/10.1371/journal.ppat.1000594
Rong, Rong, Li, Bing, Lynch, Rebecca M., Haaland, Richard E., Murphy, Megan K., Mulenga, Joseph, Allen, Susan A., Pinter, Abraham, Shaw, George M., Hunter, Eric, Robinson, James E., Gnanakaran, S., and Derdeyn, Cynthia A. Fri .
"Escape from Autologous Neutralizing Antibodies in Acute/Early Subtype C HIV-1 Infection Requires Multiple Pathways". United States. https://doi.org/10.1371/journal.ppat.1000594. https://www.osti.gov/servlets/purl/1627894.
@article{osti_1627894,
title = {Escape from Autologous Neutralizing Antibodies in Acute/Early Subtype C HIV-1 Infection Requires Multiple Pathways},
author = {Rong, Rong and Li, Bing and Lynch, Rebecca M. and Haaland, Richard E. and Murphy, Megan K. and Mulenga, Joseph and Allen, Susan A. and Pinter, Abraham and Shaw, George M. and Hunter, Eric and Robinson, James E. and Gnanakaran, S. and Derdeyn, Cynthia A.},
abstractNote = {One aim for an HIV vaccine is to elicit neutralizing antibodies (Nab) that can limit replication of genetically diverse viruses and prevent establishment of a new infection. Thus, identifying the strengths and weaknesses of Nab during the early stages of natural infection could prove useful in achieving this goal. Here we demonstrate that viral escape readily occurred despite the development of high titer autologous Nab in two subjects with acute/early subtype C infection. To provide a detailed portrayal of the escape pathways, Nab resistant variants identified at multiple time points were used to create a series of envelope (Env) glycoprotein chimeras and mutants within the background of a corresponding newly transmitted Env. In one subject, Nab escape was driven predominantly by changes in the region of gp120 that extends from the beginning of the V3 domain to the end of the V5 domain (V3V5). However, Nab escape pathways in this subject oscillated and at times required cooperation between V1V2 and the gp41 ectodomain. In the second subject, escape was driven by changes in V1V2. This V1V2-dependent escape pathway was retained over time, and its utility was reflected in the virus’s ability to escape from two distinct monoclonal antibodies (Mabs) derived from this same patient via introduction of a single potential N-linked glycosylation site in V2. Spatial representation of the sequence changes in gp120 suggested that selective pressure acted upon the same regions of Env in these two subjects, even though the Env domains that drove escape were different. Together the findings argue that a single mutational pathway is not sufficient to confer escape in early subtype C HIV-1 infection, and support a model in which multiple strategies, including potential glycan shifts, direct alteration of an epitope sequence, and cooperative Env domain conformational masking, are used to evade neutralization.},
doi = {10.1371/journal.ppat.1000594},
journal = {PLoS Pathogens},
number = 9,
volume = 5,
place = {United States},
year = {Fri Sep 18 00:00:00 EDT 2009},
month = {Fri Sep 18 00:00:00 EDT 2009}
}
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Positive Selection at Key Residues in the HIV Envelope Distinguishes Broad and Strain-Specific Plasma Neutralizing Antibodies
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Single-Genome Sequencing of Hepatitis C Virus in Donor-Recipient Pairs Distinguishes Modes and Models of Virus Transmission and Early Diversification
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The Janus Face of Follicular T Helper Cells in Chronic Viral Infections
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Identification of broadly neutralizing antibody epitopes in the HIV-1 envelope glycoprotein using evolutionary models
text, January 2013
- Lacerda, Miguel; Moore, Penny; Ngandu, Nobubelo
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