Evidence map›Paper›PMID 38349178›Full record

ArticleClinical and translational gastroenterology2024

Higher and Sustained Cell-Mediated Immune Responses After 3 Doses of mRNA COVID-19 Vaccine in Patients With Inflammatory Bowel Disease on Anti-Tumor Necrosis Factor Therapy.

Freddy Caldera, Stacey Rolak, Francis A Farraye, Brian M Necela, Davitte Cogen, Emily E Zona, Trevor L Schell, Oscar Ramirez Ramirez, Mazen Almasry, Kelly Chun and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 4 institutions in 1 country.

Freddy CalderaDepartment of Medicine, Division of Gastroenterology and Hepatology, University of Wisconsin School of Medicine & Public Health, Madison, Wisconsin, USA.ORCID 0000-0003-1960-6611
Stacey RolakDepartment of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Francis A FarrayeInflammatory Bowel Disease Center, Department of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.
Brian M NecelaDepartment of Immunology, Mayo Clinic, Jacksonville, Florida, USA.
Davitte CogenDepartment of Immunology, Mayo Clinic, Jacksonville, Florida, USA.
Emily E ZonaUniversity of Wisconsin School of Medicine and Public Health, Madison, WI.
Trevor L SchellDepartment of Internal Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Oscar Ramirez RamirezDepartment of Internal Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Mazen AlmasryDepartment of Internal Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Kelly ChunLabCorp, R&D and Specialty Medicine, Calabasas, CA, USA.
Mary S HayneySchool of Pharmacy, University of Wisconsin School of Medicine & Public Health, Madison, Wisconsin, USA.
Keith L KnutsonDepartment of Immunology, Mayo Clinic, Jacksonville, Florida, USA.
University of Wisconsin–Madison · USJacksonville College · USLabCorp (United States) · USMayo Clinic · US

Funding

American College of Gastroenterology
6 · The paper itself

Abstract

introductionStudies suggest that the generation of durable T-cell immunity following coronavirus disease 2019 (COVID-19) vaccination protects against severe disease. The aim of this study was to measure cell-mediated immune response (CMIR) 1-2 months and 6 months after a third dose of a COVID-19 mRNA vaccine.

methodsThis prospective study (HumoRal and CellULar initial and Sustained immunogenicity in patients with inflammatory bowel disease [IBD]) evaluated CMIR at 28-65 days (t 1 ) after dose 2, 28-65 days (t 2 ) (n = 183) and 6 months (±45 days) (t 3 ) (n = 167) after a third dose of an mRNA COVID-19 vaccine. A small cohort had blood sample available 28-65 days (t 4 ) (n = 55) after a fourth dose. Primary outcomes were CMIR at (t 2 ) and (t 3 ). Secondary outcomes included the effect of immunosuppressing IBD medications on CMIR and response at (t 4 ).

resultsAll patients had measurable CMIR at all time points. CMIR increased at t 2 compared with that at t 1 (median 1,467 responding cells per million (interquartile range [IQR] 410-5,971) vs 313 (94-960) P < 0.001). There was no significant waning in t 2 vs t 3 or significant boosting at t 4 . Those on anti-tumor necrosis factor monotherapy had a higher CMIR compared with those not on this therapy at t 2 (4,132 [IQR 1,136-8,795] vs 869 [IQR 343-3,221] P < 0.001) and t 3 (2,843 [IQR 596-6,459] vs 654 [IQR 143-2,067] P < 0.001). In univariable analysis, anti-tumor necrosis factor monotherapy was associated with a higher CMIR at t 2 ( P < 0.001) and t 3 ( P < 0.001) and confirmed in a multivariable model ( P < 0.001). DISCUSSION: A third dose of a COVID-19 vaccine boosts CMIR, and the response is sustained in patients with IBD.

Indexed as

COVID-19COVID-19 VaccinesImmunity, CellularInflammatory Bowel DiseasesSARS-CoV-2AdultAgedAntibodies, ViralBNT162 VaccineFemaleHumansImmunogenicity, VaccineImmunosuppressive AgentsMaleMiddle AgedProspective StudiesAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunosuppressive AgentsTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsCrohn's diseaseimmune responseimmunologyulcerative colitis

Identifiers

PMID38349178
PMCPMC11042770
OpenAlexW4391777894

What OpenQuestion holds

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LicenceCC BY
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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.