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A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117
Broadly neutralising antibodies (bNAbs) are a promising new therapy for the treatment of HIV infection. However, the effective use of bNAbs is impacted by the presence of preexisting virological resistance and the potential to develop new resistance during treatment. With several bNAb clinical trial...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594129/ https://www.ncbi.nlm.nih.gov/pubmed/36178770 http://dx.doi.org/10.1097/COH.0000000000000764 |
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author | Zacharopoulou, Panagiota Ansari, M. Azim Frater, John |
author_facet | Zacharopoulou, Panagiota Ansari, M. Azim Frater, John |
author_sort | Zacharopoulou, Panagiota |
collection | PubMed |
description | Broadly neutralising antibodies (bNAbs) are a promising new therapy for the treatment of HIV infection. However, the effective use of bNAbs is impacted by the presence of preexisting virological resistance and the potential to develop new resistance during treatment. With several bNAb clinical trials underway, sensitive and scalable assays are needed to screen for resistance. This review summarises the data on resistance from published clinical trials using the bNAbs 10-1074 and 3BNC117 and evaluates current approaches for detecting bNAb sensitivity as well as their limitations. RECENT FINDINGS: Analyses of samples from clinical trials of 10-1074 and 3BNC117 reveal viral mutations that emerge on therapy which may result in bNAb resistance. These mutations are also found in some potential study participants prior to bNAb exposure. These clinical data are further informed by ex-vivo neutralisation assays which offer an alternative measure of resistance and allow more detailed interrogation of specific viral mutations. However, the limited amount of publicly available data and the need for better understanding of other viral features that may affect bNAb binding mean there is no widely accepted approach to measuring bNAb resistance. SUMMARY: Resistance to the bNAbs 10-1074 and 3BNC117 may significantly impact clinical outcome following their therapeutic administration. Predicting bNAb resistance may help to lower the risk of treatment failure and therefore a robust methodology to screen for bNAb sensitivity is needed. |
format | Online Article Text |
id | pubmed-9594129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-95941292022-10-27 A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 Zacharopoulou, Panagiota Ansari, M. Azim Frater, John Curr Opin HIV AIDS THERAPEUTIC VACCINES: Edited by Beatriz Mothe Broadly neutralising antibodies (bNAbs) are a promising new therapy for the treatment of HIV infection. However, the effective use of bNAbs is impacted by the presence of preexisting virological resistance and the potential to develop new resistance during treatment. With several bNAb clinical trials underway, sensitive and scalable assays are needed to screen for resistance. This review summarises the data on resistance from published clinical trials using the bNAbs 10-1074 and 3BNC117 and evaluates current approaches for detecting bNAb sensitivity as well as their limitations. RECENT FINDINGS: Analyses of samples from clinical trials of 10-1074 and 3BNC117 reveal viral mutations that emerge on therapy which may result in bNAb resistance. These mutations are also found in some potential study participants prior to bNAb exposure. These clinical data are further informed by ex-vivo neutralisation assays which offer an alternative measure of resistance and allow more detailed interrogation of specific viral mutations. However, the limited amount of publicly available data and the need for better understanding of other viral features that may affect bNAb binding mean there is no widely accepted approach to measuring bNAb resistance. SUMMARY: Resistance to the bNAbs 10-1074 and 3BNC117 may significantly impact clinical outcome following their therapeutic administration. Predicting bNAb resistance may help to lower the risk of treatment failure and therefore a robust methodology to screen for bNAb sensitivity is needed. Lippincott Williams & Wilkins 2022-11 2022-09-27 /pmc/articles/PMC9594129/ /pubmed/36178770 http://dx.doi.org/10.1097/COH.0000000000000764 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | THERAPEUTIC VACCINES: Edited by Beatriz Mothe Zacharopoulou, Panagiota Ansari, M. Azim Frater, John A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 |
title | A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 |
title_full | A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 |
title_fullStr | A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 |
title_full_unstemmed | A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 |
title_short | A calculated risk: Evaluating HIV resistance to the broadly neutralising antibodies10-1074 and 3BNC117 |
title_sort | calculated risk: evaluating hiv resistance to the broadly neutralising antibodies10-1074 and 3bnc117 |
topic | THERAPEUTIC VACCINES: Edited by Beatriz Mothe |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9594129/ https://www.ncbi.nlm.nih.gov/pubmed/36178770 http://dx.doi.org/10.1097/COH.0000000000000764 |
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