Highly active HIV antibody restricts development of viral resistance
- Date:
- January 31, 2020
- Source:
- German Center for Infection Research
- Summary:
- A research team has identified a new highly active antibody targeting HIV. Whereas the development of viral resistance limits the efficacy of previously described HIV antibodies, the newly identified antibody 1-18 can continuously suppress viral replication. 1-18 there-fore has high potential for successful application in the prevention and treatment of HIV infection.
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Antiretroviral drugs are the gold standard for the treatment of HIV infection. They are highly effective in suppressing replication of the virus but require lifelong daily application and can be associated with side effects. Due to the high mutability of HIV and its capacity for rapid adaptation, combinations of antiretroviral agents are required to prevent the development of drug re-sistance and treatment failure.
Broadly neutralizing antibodies targeting HIV
Broadly neutralizing antibodies are a focus of ongoing research on novel op-tions for the treatment and prevention of HIV infection. Their mode of action substantially differs from regular antiretroviral drugs, as antibodies target the virus through specific binding of HIV surface proteins.
Clinical trials have demonstrated the potential of broadly neutralizing antibod-ies by reducing the viral load in the blood of HIV-infected individuals. Similar to antiretroviral drugs, however, the effects of single antibodies were only temporary because of the development of viral resistance.
Identification of the highly potent antibody 1-18
Scientists at the University Hospital Cologne have now identified a novel anti-body called 1-18 that targets HIV. This antibody is highly potent and showed activity against 97% of the tested HIV variants. "1-18 is therefore among the best HIV neutralizing antibodies described to date," says Dr. Philipp Schom-mers, resident physician at the Department I of Internal Medicine and one of the first authors of the article.
In collaboration with colleagues at the California Institute of Technology (Pas-adena, USA), the researchers identified the mode of action of antibody 1-18 in detail. 1-18 binds and inactivates a surface structure of HIV that is particu-larly relevant because it is essential for viral infection and replication.
Effective HIV therapy using antibody 1-18
The therapeutic efficacy of the newly identified antibody 1-18 was studied using a mouse model that allows recapitulation of HIV infection as it occurs in humans. In this model, other broadly neutralizing antibodies showed only short-term effects because of the rapid development of viral resistance. In contrast, treatment with the antibody 1-18 resulted in suppression of the viral load that was maintained for the duration of therapy. "These results indicate that development of viral resistance against the new antibody 1-18 is restrict-ed when compared to other antibodies," says Dr. Henning Grüll, resident phy-sician at the Institute of Virology and also first author of the work.
Due to its high potency, the scientists consider 1-18 a promising candidate for HIV immunotherapy. "In addition, 1-18 has great potential for preventing HIV infection by passive immunization," adds Prof. Dr. Florian Klein, lead and sen-ior author of the study. Clinical trials are now planned to further investigate antibody 1-18.
Story Source:
Materials provided by German Center for Infection Research. Note: Content may be edited for style and length.
Journal Reference:
- Philipp Schommers, Henning Gruell, Morgan E. Abernathy, My-Kim Tran, Adam S. Dingens, Harry B. Gristick, Christopher O. Barnes, Till Schoofs, Maike Schlotz, Kanika Vanshylla, Christoph Kreer, Daniela Weiland, Udo Holtick, Christof Scheid, Markus M. Valter, Marit J. van Gils, Rogier W. Sanders, Jörg J. Vehreschild, Oliver A. Cornely, Clara Lehmann, Gerd Fätkenheuer, Michael S. Seaman, Jesse D. Bloom, Pamela J. Bjorkman, Florian Klein. Restriction of HIV-1 Escape by a Highly Broad and Potent Neutralizing Antibody. Cell, 2020; 180 (3): 471 DOI: 10.1016/j.cell.2020.01.010
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