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Macrophage colony‐stimulating factor as a weapon against cytomegalovirus

Cytomegalovirus (CMV) infection is one of the severe opportunistic infections faced by severely immunocompromised patients. High viral loads cause tissue‐invasive disease and expose to death or various indirect effects. Substantial progress was made in monitoring active infection, and antiviral drug...

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Autor principal: Solary, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10630862/
https://www.ncbi.nlm.nih.gov/pubmed/37697915
http://dx.doi.org/10.15252/emmm.202318319
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author Solary, Eric
author_facet Solary, Eric
author_sort Solary, Eric
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description Cytomegalovirus (CMV) infection is one of the severe opportunistic infections faced by severely immunocompromised patients. High viral loads cause tissue‐invasive disease and expose to death or various indirect effects. Substantial progress was made in monitoring active infection, and antiviral drugs were developed. However, dose‐limiting toxicities and genotypic resistance limit therapeutic efficacy and vaccine development is hampered by the complex biology of the virus. In this issue of EMBO Molecular Medicine, Kandalla et al (2023) suggest an innovative strategy using the cytokine macrophage colony‐stimulating factor (M‐CSF) whose clinical development was left behind two decades ago. By stimulating an endogenous immune defense mechanism, M‐CSF promotes viral clearance in a mouse model of hematopoietic stem cell transplantation, without impairing stem cell engraftment. These results reactivate the interest in the potential therapeutic use of this cytokine.
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spelling pubmed-106308622023-11-15 Macrophage colony‐stimulating factor as a weapon against cytomegalovirus Solary, Eric EMBO Mol Med News & Views Cytomegalovirus (CMV) infection is one of the severe opportunistic infections faced by severely immunocompromised patients. High viral loads cause tissue‐invasive disease and expose to death or various indirect effects. Substantial progress was made in monitoring active infection, and antiviral drugs were developed. However, dose‐limiting toxicities and genotypic resistance limit therapeutic efficacy and vaccine development is hampered by the complex biology of the virus. In this issue of EMBO Molecular Medicine, Kandalla et al (2023) suggest an innovative strategy using the cytokine macrophage colony‐stimulating factor (M‐CSF) whose clinical development was left behind two decades ago. By stimulating an endogenous immune defense mechanism, M‐CSF promotes viral clearance in a mouse model of hematopoietic stem cell transplantation, without impairing stem cell engraftment. These results reactivate the interest in the potential therapeutic use of this cytokine. John Wiley and Sons Inc. 2023-09-12 /pmc/articles/PMC10630862/ /pubmed/37697915 http://dx.doi.org/10.15252/emmm.202318319 Text en © 2023 The Author. Published under the terms of the CC BY 4.0 license 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 News & Views
Solary, Eric
Macrophage colony‐stimulating factor as a weapon against cytomegalovirus
title Macrophage colony‐stimulating factor as a weapon against cytomegalovirus
title_full Macrophage colony‐stimulating factor as a weapon against cytomegalovirus
title_fullStr Macrophage colony‐stimulating factor as a weapon against cytomegalovirus
title_full_unstemmed Macrophage colony‐stimulating factor as a weapon against cytomegalovirus
title_short Macrophage colony‐stimulating factor as a weapon against cytomegalovirus
title_sort macrophage colony‐stimulating factor as a weapon against cytomegalovirus
topic News & Views
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10630862/
https://www.ncbi.nlm.nih.gov/pubmed/37697915
http://dx.doi.org/10.15252/emmm.202318319
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