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Current approaches to HIV vaccine development: a narrative review

INTRODUCTION: The development of an effective vaccine to protect against HIV is a longstanding global health need complicated by challenges inherent to HIV biology and to the execution of vaccine efficacy testing in the context of evolving biomedical prevention interventions. This review describes l...

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Autores principales: Kim, Jiae, Vasan, Sandhya, Kim, Jerome H., Ake, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606871/
https://www.ncbi.nlm.nih.gov/pubmed/34806296
http://dx.doi.org/10.1002/jia2.25793
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author Kim, Jiae
Vasan, Sandhya
Kim, Jerome H.
Ake, Julie A.
author_facet Kim, Jiae
Vasan, Sandhya
Kim, Jerome H.
Ake, Julie A.
author_sort Kim, Jiae
collection PubMed
description INTRODUCTION: The development of an effective vaccine to protect against HIV is a longstanding global health need complicated by challenges inherent to HIV biology and to the execution of vaccine efficacy testing in the context of evolving biomedical prevention interventions. This review describes lessons learnt from previous efficacy trials, highlights unanswered questions, and surveys new approaches in vaccine development addressing these gaps. METHODS: We conducted a targeted peer‐reviewed literature search of articles and conference abstracts from 1989 through 2021 for HIV vaccine studies and clinical trials. The US National Library of Medicine's Clinical Trials database was accessed to further identify clinical trials involving HIV vaccines. The content of the review was also informed by the authors’ own experience and engagement with collaborators in HIV vaccine research. DISCUSSION: The HIV vaccine field has successfully developed multiple vaccine platforms through advanced clinical studies; however, the modest efficacy signal of the RV144 Thai trial remains the only demonstration of HIV vaccine protection in humans. Current vaccine strategies include prime‐boost strategies to improve elicitation of immune correlates derived from RV144, combination mosaic antigens, novel viral vectors, antigens designed to elicit broadly neutralizing antibody, new nucleic acid platforms and potent adjuvants to enhance immunogenicity across multiple classes of emerging vaccine candidates. CONCLUSIONS: HIV vaccine developers have applied lessons learnt from previous successes and failures to innovative vaccine design approaches. These strategies have yielded novel mosaic antigen constructs now in efficacy testing, produced a diverse pipeline of early‐stage immunogens and novel adjuvants, and advanced the field towards a globally effective HIV vaccine.
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spelling pubmed-86068712021-11-29 Current approaches to HIV vaccine development: a narrative review Kim, Jiae Vasan, Sandhya Kim, Jerome H. Ake, Julie A. J Int AIDS Soc Supplement: Reviews INTRODUCTION: The development of an effective vaccine to protect against HIV is a longstanding global health need complicated by challenges inherent to HIV biology and to the execution of vaccine efficacy testing in the context of evolving biomedical prevention interventions. This review describes lessons learnt from previous efficacy trials, highlights unanswered questions, and surveys new approaches in vaccine development addressing these gaps. METHODS: We conducted a targeted peer‐reviewed literature search of articles and conference abstracts from 1989 through 2021 for HIV vaccine studies and clinical trials. The US National Library of Medicine's Clinical Trials database was accessed to further identify clinical trials involving HIV vaccines. The content of the review was also informed by the authors’ own experience and engagement with collaborators in HIV vaccine research. DISCUSSION: The HIV vaccine field has successfully developed multiple vaccine platforms through advanced clinical studies; however, the modest efficacy signal of the RV144 Thai trial remains the only demonstration of HIV vaccine protection in humans. Current vaccine strategies include prime‐boost strategies to improve elicitation of immune correlates derived from RV144, combination mosaic antigens, novel viral vectors, antigens designed to elicit broadly neutralizing antibody, new nucleic acid platforms and potent adjuvants to enhance immunogenicity across multiple classes of emerging vaccine candidates. CONCLUSIONS: HIV vaccine developers have applied lessons learnt from previous successes and failures to innovative vaccine design approaches. These strategies have yielded novel mosaic antigen constructs now in efficacy testing, produced a diverse pipeline of early‐stage immunogens and novel adjuvants, and advanced the field towards a globally effective HIV vaccine. John Wiley and Sons Inc. 2021-11-21 /pmc/articles/PMC8606871/ /pubmed/34806296 http://dx.doi.org/10.1002/jia2.25793 Text en © 2021 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement: Reviews
Kim, Jiae
Vasan, Sandhya
Kim, Jerome H.
Ake, Julie A.
Current approaches to HIV vaccine development: a narrative review
title Current approaches to HIV vaccine development: a narrative review
title_full Current approaches to HIV vaccine development: a narrative review
title_fullStr Current approaches to HIV vaccine development: a narrative review
title_full_unstemmed Current approaches to HIV vaccine development: a narrative review
title_short Current approaches to HIV vaccine development: a narrative review
title_sort current approaches to hiv vaccine development: a narrative review
topic Supplement: Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606871/
https://www.ncbi.nlm.nih.gov/pubmed/34806296
http://dx.doi.org/10.1002/jia2.25793
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