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Advances in the treatment of cytomegalovirus

BACKGROUND: Human cytomegalovirus (HCMV) is a threat to immunologically weak patients. HCMV cannot yet be eliminated with a vaccine, despite recent advances. SOURCES OF DATA: Sources of data are recently published research papers and reviews about HCMV treatments. AREAS OF AGREEMENT: Current antivir...

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Detalles Bibliográficos
Autores principales: Krishna, B A, Wills, M R, Sinclair, J H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821982/
https://www.ncbi.nlm.nih.gov/pubmed/31580403
http://dx.doi.org/10.1093/bmb/ldz031
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author Krishna, B A
Wills, M R
Sinclair, J H
author_facet Krishna, B A
Wills, M R
Sinclair, J H
author_sort Krishna, B A
collection PubMed
description BACKGROUND: Human cytomegalovirus (HCMV) is a threat to immunologically weak patients. HCMV cannot yet be eliminated with a vaccine, despite recent advances. SOURCES OF DATA: Sources of data are recently published research papers and reviews about HCMV treatments. AREAS OF AGREEMENT: Current antivirals target the UL54 DNA polymerase and are limited by nephrotoxicity and viral resistance. Promisingly, letermovir targets the HCMV terminase complex and has been recently approved by the FDA and EMA. AREAS OF CONTROVERSY: Should we screen newborns for HCMV, and use antivirals to treat sensorineural hearing loss after congenital HCMV infection? GROWING POINTS: Growing points are developing drugs against latently infected cells. In addition to small molecule inhibitors, a chemokine-based fusion toxin protein, F49A-FTP, has shown promise in killing both lytically and latently infected cells. AREAS TIMELY FOR DEVELOPING RESEARCH: We need to understand what immune responses are required to control HCMV, and how best to raise these immune responses with a vaccine.
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spelling pubmed-68219822019-11-04 Advances in the treatment of cytomegalovirus Krishna, B A Wills, M R Sinclair, J H Br Med Bull Invited Review BACKGROUND: Human cytomegalovirus (HCMV) is a threat to immunologically weak patients. HCMV cannot yet be eliminated with a vaccine, despite recent advances. SOURCES OF DATA: Sources of data are recently published research papers and reviews about HCMV treatments. AREAS OF AGREEMENT: Current antivirals target the UL54 DNA polymerase and are limited by nephrotoxicity and viral resistance. Promisingly, letermovir targets the HCMV terminase complex and has been recently approved by the FDA and EMA. AREAS OF CONTROVERSY: Should we screen newborns for HCMV, and use antivirals to treat sensorineural hearing loss after congenital HCMV infection? GROWING POINTS: Growing points are developing drugs against latently infected cells. In addition to small molecule inhibitors, a chemokine-based fusion toxin protein, F49A-FTP, has shown promise in killing both lytically and latently infected cells. AREAS TIMELY FOR DEVELOPING RESEARCH: We need to understand what immune responses are required to control HCMV, and how best to raise these immune responses with a vaccine. Oxford University Press 2019-09 2019-10-03 /pmc/articles/PMC6821982/ /pubmed/31580403 http://dx.doi.org/10.1093/bmb/ldz031 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Review
Krishna, B A
Wills, M R
Sinclair, J H
Advances in the treatment of cytomegalovirus
title Advances in the treatment of cytomegalovirus
title_full Advances in the treatment of cytomegalovirus
title_fullStr Advances in the treatment of cytomegalovirus
title_full_unstemmed Advances in the treatment of cytomegalovirus
title_short Advances in the treatment of cytomegalovirus
title_sort advances in the treatment of cytomegalovirus
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821982/
https://www.ncbi.nlm.nih.gov/pubmed/31580403
http://dx.doi.org/10.1093/bmb/ldz031
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