Evidence map›Paper›PMID 29618720›Full record

Observational studyClinical and translational gastroenterology2018

Anti-TNF and thiopurine therapy in pregnant IBD patients does not significantly alter a panel of B-cell and T-cell subsets in 1-year-old infants.

Michael G Kattah, Jeffrey M Milush, Trevor Burt, Robert P McCabe, Michael I Whang, Averil Ma, Uma Mahadevan

Erratum issuedOpen access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Clinical and translational gastroenterology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Safety of in utero exposure to maternal IBD pharmacotherapies.Nature reviews. Gastroenterology & hepatology · 2022
    Article
  8. Immune function in newborns withFrontiers in pediatrics · 2022
    Article
  9. Review
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Michael G KattahDepartment of Medicine, Division of Gastroenterology, University of California San Francisco, San Francisco, CA, USA. michael.kattah@ucsf.edu.
Jeffrey M MilushDepartment of Medicine, Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
Trevor BurtDepartment of Pediatrics, Division of Neonatology, University of California San Francisco, San Francisco, CA, USA.
Robert P McCabeDepartment of Medicine, Division of Gastroenterology, University of Minnesota, Minneapolis, MN, USA.
Michael I WhangDepartment of Medicine, Division of Gastroenterology, University of California San Francisco, San Francisco, CA, USA.
Averil MaDepartment of Medicine, Division of Gastroenterology, University of California San Francisco, San Francisco, CA, USA.
Uma MahadevanDepartment of Medicine, Division of Gastroenterology, University of California San Francisco, San Francisco, CA, USA.
University of California, San Francisco · USUniversity of Minnesota · US

Funding

Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS · 1988 to 2026
$93.6M
TRAINING PROGRAM IN DISGESTIVE DISEASES AND NUTRITIONT32DK007007 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AVERIL I MA · 1986 to 2026
$6.4M
A20 Mediated Regulation of Colitis and SpondyloarthritisR01DK095693 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, AVERIL I · 2012 to 2021
$3.1M
NIAID NIH HHS P30 AI027763NIDDK NIH HHS R01 DK095693NIDDK NIH HHS T32 DK007007
6 · The paper itself

Abstract

objectivesInfants exposed to combination therapy with anti-tumor necrosis factor (anti-TNF) agents and thiopurines may exhibit increased infections at 1 year of age compared to unexposed infants. We hypothesized that this increased risk of infection is due to abnormal development of the newborn immune system.

methodsWe immunophenotyped B-cell and T-cell subsets using multiparameter flow cytometry in 1-year-old infants whose mothers were exposed to therapeutic agents for IBD. We analyzed samples from infants exposed to infliximab (IFX) or adalimumab (ADA) monotherapy (IFX/ADA, n = 11), certolizumab pegol (CZP) monotherapy (CZP, n = 4), IFX or ADA plus thiopurine combination therapy (IFX/ADA + IM, n = 4), and CZP plus thiopurine combination therapy (CZP + IM, n = 2).

resultsPercentages of B cells, CD4

conclusionsMultiparameter immunophenotyping of major B-cell and T-cell subsets suggests that the adaptive newborn immune system develops largely unaltered after exposure to combination therapy as compared to anti-TNF monotherapy.

Indexed as

Prenatal Exposure Delayed EffectsAdalimumabAdultAnimalsAnti-Inflammatory AgentsB-Lymphocyte SubsetsCertolizumab PegolDrug Therapy, CombinationFemaleHumansImmunologic FactorsImmunophenotypingInfantInfectionsInflammatory Bowel DiseasesInfliximabAdalimumabAnti-Inflammatory AgentsCertolizumab PegolImmunologic FactorsInfliximabMercaptopurineTumor Necrosis Factor-alpha

Identifiers

PMID29618720
PMCPMC5886978
OpenAlexW2795836679

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.