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Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response

There has been a surge in studies implicating a role of vaginal microbiota in spontaneous preterm birth (sPTB), but most are associative without mechanistic insight. Here we show a comprehensive approach to understand the causative factors of preterm birth, based on the integration of longitudinal v...

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Autores principales: Chan, Denise, Bennett, Phillip R., Lee, Yun S., Kundu, Samit, Teoh, T. G., Adan, Malko, Ahmed, Saqa, Brown, Richard G., David, Anna L., Lewis, Holly V., Gimeno-Molina, Belen, Norman, Jane E., Stock, Sarah J., Terzidou, Vasso, Kropf, Pascale, Botto, Marina, MacIntyre, David A., Sykes, Lynne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861006/
https://www.ncbi.nlm.nih.gov/pubmed/35190561
http://dx.doi.org/10.1038/s41467-022-28620-1
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author Chan, Denise
Bennett, Phillip R.
Lee, Yun S.
Kundu, Samit
Teoh, T. G.
Adan, Malko
Ahmed, Saqa
Brown, Richard G.
David, Anna L.
Lewis, Holly V.
Gimeno-Molina, Belen
Norman, Jane E.
Stock, Sarah J.
Terzidou, Vasso
Kropf, Pascale
Botto, Marina
MacIntyre, David A.
Sykes, Lynne
author_facet Chan, Denise
Bennett, Phillip R.
Lee, Yun S.
Kundu, Samit
Teoh, T. G.
Adan, Malko
Ahmed, Saqa
Brown, Richard G.
David, Anna L.
Lewis, Holly V.
Gimeno-Molina, Belen
Norman, Jane E.
Stock, Sarah J.
Terzidou, Vasso
Kropf, Pascale
Botto, Marina
MacIntyre, David A.
Sykes, Lynne
author_sort Chan, Denise
collection PubMed
description There has been a surge in studies implicating a role of vaginal microbiota in spontaneous preterm birth (sPTB), but most are associative without mechanistic insight. Here we show a comprehensive approach to understand the causative factors of preterm birth, based on the integration of longitudinal vaginal microbiota and cervicovaginal fluid (CVF) immunophenotype data collected from 133 women at high-risk of sPTB. We show that vaginal depletion of Lactobacillus species and high bacterial diversity leads to increased mannose binding lectin (MBL), IgM, IgG, C3b, C5, IL-8, IL-6 and IL-1β and to increased risk of sPTB. Cervical shortening, which often precedes preterm birth, is associated with Lactobacillus iners and elevated levels of IgM, C3b, C5, C5a and IL-6. These data demonstrate a role for the complement system in microbial-driven sPTB and provide a scientific rationale for the development of live biotherapeutics and complement therapeutics to prevent sPTB.
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spelling pubmed-88610062022-03-17 Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response Chan, Denise Bennett, Phillip R. Lee, Yun S. Kundu, Samit Teoh, T. G. Adan, Malko Ahmed, Saqa Brown, Richard G. David, Anna L. Lewis, Holly V. Gimeno-Molina, Belen Norman, Jane E. Stock, Sarah J. Terzidou, Vasso Kropf, Pascale Botto, Marina MacIntyre, David A. Sykes, Lynne Nat Commun Article There has been a surge in studies implicating a role of vaginal microbiota in spontaneous preterm birth (sPTB), but most are associative without mechanistic insight. Here we show a comprehensive approach to understand the causative factors of preterm birth, based on the integration of longitudinal vaginal microbiota and cervicovaginal fluid (CVF) immunophenotype data collected from 133 women at high-risk of sPTB. We show that vaginal depletion of Lactobacillus species and high bacterial diversity leads to increased mannose binding lectin (MBL), IgM, IgG, C3b, C5, IL-8, IL-6 and IL-1β and to increased risk of sPTB. Cervical shortening, which often precedes preterm birth, is associated with Lactobacillus iners and elevated levels of IgM, C3b, C5, C5a and IL-6. These data demonstrate a role for the complement system in microbial-driven sPTB and provide a scientific rationale for the development of live biotherapeutics and complement therapeutics to prevent sPTB. Nature Publishing Group UK 2022-02-21 /pmc/articles/PMC8861006/ /pubmed/35190561 http://dx.doi.org/10.1038/s41467-022-28620-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chan, Denise
Bennett, Phillip R.
Lee, Yun S.
Kundu, Samit
Teoh, T. G.
Adan, Malko
Ahmed, Saqa
Brown, Richard G.
David, Anna L.
Lewis, Holly V.
Gimeno-Molina, Belen
Norman, Jane E.
Stock, Sarah J.
Terzidou, Vasso
Kropf, Pascale
Botto, Marina
MacIntyre, David A.
Sykes, Lynne
Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
title Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
title_full Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
title_fullStr Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
title_full_unstemmed Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
title_short Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
title_sort microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861006/
https://www.ncbi.nlm.nih.gov/pubmed/35190561
http://dx.doi.org/10.1038/s41467-022-28620-1
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