Evidence map›Paper›PMID 38802950›Full record

ArticleMicrobiome2024

The interrelation between microbial immunoglobulin coating, vaginal microbiota, ethnicity, and preterm birth.

H J Schuster, A C Breedveld, S P F Matamoros, R van Eekelen, R C Painter, M Kok, P J Hajenius, P H M Savelkoul, M van Egmond, R van Houdt

Abstract read
In one paragraph

Article in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. IgA and the gut-vagina axis.Frontiers in immunology · 2025
    Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

H J SchusterAmsterdam UMC location Vrije Universiteit Amsterdam, Medical Microbiology and Infection Control, Boelelaan 1117, Amsterdam, The Netherlands. h.schuster@amsterdamumc.nl.
A C BreedveldAmsterdam institute for Immunology and Infectious Diseases, Amsterdam, The Netherlands.
S P F MatamorosAmsterdam UMC location Vrije Universiteit Amsterdam, Medical Microbiology and Infection Control, Boelelaan 1117, Amsterdam, The Netherlands.
R van EekelenAmsterdam UMC location Vrije Universiteit Amsterdam, Epidemiology and Data Science, Boelelaan 1117, Amsterdam, The Netherlands.
R C PainterAmsterdam Reproduction and Development, Amsterdam, The Netherlands.
M KokAmsterdam UMC location University of Amsterdam, Obstetrics and Gynecology, Meibergdreef 9, Amsterdam, The Netherlands.
P J HajeniusAmsterdam UMC location University of Amsterdam, Obstetrics and Gynecology, Meibergdreef 9, Amsterdam, The Netherlands.
P H M SavelkoulAmsterdam UMC location Vrije Universiteit Amsterdam, Medical Microbiology and Infection Control, Boelelaan 1117, Amsterdam, The Netherlands.
M van EgmondAmsterdam institute for Immunology and Infectious Diseases, Amsterdam, The Netherlands.
R van HoudtAmsterdam UMC location Vrije Universiteit Amsterdam, Medical Microbiology and Infection Control, Boelelaan 1117, Amsterdam, The Netherlands.

Funding

Amsterdam Reproduction and Development AR&D2016ZonMw VICI 91814650
6 · The paper itself

Abstract

backgroundVaginal microbiota composition is associated with spontaneous preterm birth (sPTB), depending on ethnicity. Host-microbiota interactions are thought to play an important underlying role in this association between ethnicity, vaginal microbiota and sPTB.

methodsIn a prospective cohort of nulliparous pregnant women, we assessed vaginal microbiota composition, vaginal immunoglobulins (Igs), and local inflammatory markers. We performed a nested case-control study with 19 sPTB cases, matched based on ethnicity and midwifery practice to 19 term controls.

resultsOf the 294 included participants, 23 pregnancies ended in sPTB. We demonstrated that Lactobacillus iners-dominated microbiota, diverse microbiota, and ethnicity were all independently associated with sPTB. Microbial Ig coating was associated with both microbiota composition and ethnicity, but a direct association with sPTB was lacking. Microbial IgA and IgG coating were lowest in diverse microbiota, especially in women of any ethnic minority. When correcting for microbiota composition, increased microbial Ig coating correlated with increased inflammation.

conclusionIn these nulliparous pregnant women, vaginal microbiota composition is strongly associated with sPTB. Our results support that vaginal mucosal Igs might play a pivotal role in microbiota composition, microbiota-related inflammation, and vaginal community disparity within and between ethnicities. This study provides insight in host-microbe interaction, suggesting that vaginal mucosal Igs play an immunomodulatory role similar to that in the intestinal tract. Video Abstract.

Indexed as

EthnicityLactobacillusMicrobiotaPremature BirthVaginaAdultCase-Control StudiesFemaleHost Microbial InteractionsHumansImmunoglobulin AImmunoglobulinsPregnancyProspective StudiesYoung AdultImmunoglobulin AImmunoglobulinsEthnicityHost-microbiota interactionImmunoglobulinsNulliparous womenSpontaneous preterm birthVaginal microbiota

Identifiers

PMID38802950
PMCPMC11131309

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.