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A systematic review on global RSV genetic data: Identification of knowledge gaps

Respiratory syncytial virus (RSV) is a major health problem. A better understanding of the geographical and temporal dynamics of RSV circulation will assist in tracking resistance against therapeutics currently under development. Since 2015, the field of RSV molecular epidemiology has evolved rapidl...

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Autores principales: Langedijk, Annefleur C., Harding, Eline R., Konya, Burak, Vrancken, Bram, Lebbink, Robert Jan, Evers, Anouk, Willemsen, Joukje, Lemey, Philippe, Bont, Louis J.
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/PMC9285027/
https://www.ncbi.nlm.nih.gov/pubmed/34543489
http://dx.doi.org/10.1002/rmv.2284
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author Langedijk, Annefleur C.
Harding, Eline R.
Konya, Burak
Vrancken, Bram
Lebbink, Robert Jan
Evers, Anouk
Willemsen, Joukje
Lemey, Philippe
Bont, Louis J.
author_facet Langedijk, Annefleur C.
Harding, Eline R.
Konya, Burak
Vrancken, Bram
Lebbink, Robert Jan
Evers, Anouk
Willemsen, Joukje
Lemey, Philippe
Bont, Louis J.
author_sort Langedijk, Annefleur C.
collection PubMed
description Respiratory syncytial virus (RSV) is a major health problem. A better understanding of the geographical and temporal dynamics of RSV circulation will assist in tracking resistance against therapeutics currently under development. Since 2015, the field of RSV molecular epidemiology has evolved rapidly with around 20–30 published articles per year. The objective of this systematic review is to identify knowledge gaps in recent RSV genetic literature to guide global molecular epidemiology research. We included 78 studies published between 2015 and 2020 describing 12,998 RSV sequences of which 8,233 (63%) have been uploaded to GenBank. Seventeen (22%) studies were performed in low‐ and middle‐income countries (LMICs), and seven (9%) studies sequenced whole‐genomes. Although most reported polymorphisms for monoclonal antibodies in clinical development (nirsevimab, MK‐1654) have not been tested for resistance in neutralisation essays, known resistance was detected at low levels for the nirsevimab and palivizumab binding site. High resistance was found for the suptavumab binding site. We present the first literature review of an enormous amount of RSV genetic data. The need for global monitoring of RSV molecular epidemiology becomes increasingly important in evaluating the effectiveness of monoclonal antibody candidates as they reach their final stages of clinical development. We have identified the following three knowledge gaps: whole‐genome data to study global RSV evolution, data from LMICs and data from global surveillance programs.
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spelling pubmed-92850272022-07-15 A systematic review on global RSV genetic data: Identification of knowledge gaps Langedijk, Annefleur C. Harding, Eline R. Konya, Burak Vrancken, Bram Lebbink, Robert Jan Evers, Anouk Willemsen, Joukje Lemey, Philippe Bont, Louis J. Rev Med Virol Reviews Respiratory syncytial virus (RSV) is a major health problem. A better understanding of the geographical and temporal dynamics of RSV circulation will assist in tracking resistance against therapeutics currently under development. Since 2015, the field of RSV molecular epidemiology has evolved rapidly with around 20–30 published articles per year. The objective of this systematic review is to identify knowledge gaps in recent RSV genetic literature to guide global molecular epidemiology research. We included 78 studies published between 2015 and 2020 describing 12,998 RSV sequences of which 8,233 (63%) have been uploaded to GenBank. Seventeen (22%) studies were performed in low‐ and middle‐income countries (LMICs), and seven (9%) studies sequenced whole‐genomes. Although most reported polymorphisms for monoclonal antibodies in clinical development (nirsevimab, MK‐1654) have not been tested for resistance in neutralisation essays, known resistance was detected at low levels for the nirsevimab and palivizumab binding site. High resistance was found for the suptavumab binding site. We present the first literature review of an enormous amount of RSV genetic data. The need for global monitoring of RSV molecular epidemiology becomes increasingly important in evaluating the effectiveness of monoclonal antibody candidates as they reach their final stages of clinical development. We have identified the following three knowledge gaps: whole‐genome data to study global RSV evolution, data from LMICs and data from global surveillance programs. John Wiley and Sons Inc. 2021-09-20 2022-05 /pmc/articles/PMC9285027/ /pubmed/34543489 http://dx.doi.org/10.1002/rmv.2284 Text en © 2021 The Authors. Reviews in Medical Virology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Langedijk, Annefleur C.
Harding, Eline R.
Konya, Burak
Vrancken, Bram
Lebbink, Robert Jan
Evers, Anouk
Willemsen, Joukje
Lemey, Philippe
Bont, Louis J.
A systematic review on global RSV genetic data: Identification of knowledge gaps
title A systematic review on global RSV genetic data: Identification of knowledge gaps
title_full A systematic review on global RSV genetic data: Identification of knowledge gaps
title_fullStr A systematic review on global RSV genetic data: Identification of knowledge gaps
title_full_unstemmed A systematic review on global RSV genetic data: Identification of knowledge gaps
title_short A systematic review on global RSV genetic data: Identification of knowledge gaps
title_sort systematic review on global rsv genetic data: identification of knowledge gaps
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285027/
https://www.ncbi.nlm.nih.gov/pubmed/34543489
http://dx.doi.org/10.1002/rmv.2284
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