Evidence map›Paper›PMID 42248960›Full record

ArticleNPJ vaccines2026

Response to vaccination and immune status after intrauterine exposure to immunomodulating drugs for maternal IBD.

Jantien W Wieringa, Mirjam J Esser, Matthijs D Kruizinga, Gerco den Hartog, Lyanne W Rövekamp, Esther G J Rijntjes-Jacobs, Herbert M van Wering, Gerdien A Tramper-Stranders, Willem A Dik, Marjan Kuijer and 2 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Jantien W Wieringa *Department of Pediatrics, Haaglanden Medical Center, The Hague, The Netherlands.
Mirjam J Esser *Department of Pediatrics, Haaglanden Medical Center, The Hague, The Netherlands.
Matthijs D KruizingaDepartment of Pediatrics, Haga Teaching Hospital, Juliana Children's Hospital, The Hague, The Netherlands.
Gerco den HartogCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Lyanne W RövekampDepartment of Pediatrics, Haga Teaching Hospital, Juliana Children's Hospital, The Hague, The Netherlands.
Esther G J Rijntjes-JacobsDepartment of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.
Herbert M van WeringDepartment of Pediatrics, Amphia Hospital, Breda, The Netherlands.
Gerdien A Tramper-StrandersDepartment of Pediatrics, Franciscus Gasthuis & Vlietland, Rotterdam, The Netherlands.
Willem A DikLaboratory Medical Immunology, Department of Immunology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Marjan KuijerCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Nynke Y RotsCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Gertjan J A DriessenDepartment of Pediatrics, Maastricht University Medical Center, MosaKids Children's Hospital, Maastricht, The Netherlands. gertjan.driessen@mumc.nl.ORCID http://orcid.org/0000-0002-4566-9547

Funding

Merck Sharp and Dohme 59733
6 · The paper itself

Abstract

Guidelines on inflammatory bowel disease (IBD) recommend continuing immunomodulating drugs during pregnancy, but their effects on the infant immune system remain uncertain. In this observational study, infants exposed to maternal IBD medication were vaccinated according to the Dutch National Immunization Program. We measured vaccine-specific IgG at 6 and 12 months and leukocytes, lymphocyte subsets, immunoglobulins, and infections at 2, 6, and 12 months of age. Vaccine responses and lymphocyte subsets were compared with historical cohorts and other outcomes with age-specific reference ranges. Vaccine responses following a 3 + 1 vaccination schedule were comparable to or higher than controls following a 2 + 1 schedule for all vaccine components, except filamentous haemagglutinin (FHA) and pneumococcal serotype 19 F. Neutropenia occurred more frequently than expected from reference values, but was self-limiting in all cases. The proportion of infants with T- or total B-cell lymphopenia did not differ from healthy controls. At 6 months, 9.8% of infants had mildly reduced total IgG concentrations, and low IgA was observed in 28.1%, 41.3%, and 15.4% at 2, 6, and 12 months, respectively; significantly more than expected based on reference values. The observed infection rate was similar to that reported in the literature. These findings may help develop clinical follow-up guidelines.

Identifiers

PMID42248960
PMCPMC13558638

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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.