Publication
Harnessing the protective potential of HIV-1 neutralizing antibodies.
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- Last modified
- 02/20/2025
- Type of Material
- Authors
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S Abigail Smith, Yerkes National Primate Research CenterCynthia Derdeyn, Emory University
- Language
- English
- Date
- 2016
- Publisher
- F1000Research
- Publication Version
- Copyright Statement
- © 2016 Smith SA and Derdeyn CA.
- License
- Final Published Version (URL)
- Title of Journal or Parent Work
- ISSN
- 2046-1402
- Volume
- 5
- Grant/Funding Information
- CAD and SAS are supported by NIH-R01-AI58706.
- Abstract
- Recent biological, structural, and technical advances are converging within the HIV-1 vaccine field to harness the power of antibodies for prevention and therapy. Numerous monoclonal antibodies with broad neutralizing activity against diverse HIV-1 isolates have now been identified, revealing at least five sites of vulnerability on the envelope (Env) glycoproteins. While there are practical and technological barriers blocking a clear path from broadly neutralizing antibodies (bNAb) to a protective vaccine, this is not a dead end. Scientists are revisiting old approaches with new technology, cutting new trails through unexplored territory, and paving new roads in the hopes of preventing HIV-1 infection. Other promising avenues to capitalize on the power of bNAbs are also being pursued, such as passive antibody immunotherapy and gene therapy approaches. Moreover, non-neutralizing antibodies have inhibitory activities that could have protective potential, alone or in combination with bNAbs. With a new generation of bNAbs, and a clinical trial that associated antibodies with reduced acquisition, the field is closer than ever to developing strategies to use antibodies against HIV-1.
- Author Notes
- Keywords
- Research Categories
- Health Sciences, General
- Biology, Virology
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