Evidence map›Paper›PMID 37231290›Full record

ArticleJournal of clinical immunology2023

Immune Responses 6 Months After mRNA-1273 COVID-19 Vaccination and the Effect of a Third Vaccination in Patients with Inborn Errors of Immunity.

Leanne P M van Leeuwen, Marloes Grobben, Corine H GeurtsvanKessel, Pauline M Ellerbroek, Godelieve J de Bree, Judith Potjewijd, Abraham Rutgers, Hetty Jolink, Frank L van de Veerdonk, Marit J van Gils and 3 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

13 authors at 7 institutions in 1 country.

Leanne P M van Leeuwen *Department of Viroscience, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Marloes Grobben *Department of Medical Microbiology and Infection Prevention, Amsterdam Institute for Infection and Immunity, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Corine H GeurtsvanKessel *Department of Viroscience, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Pauline M Ellerbroek *Department of Internal Medicine, UMC Utrecht, Utrecht, The Netherlands.
Godelieve J de Bree *Department of Infectious Diseases, Amsterdam UMC, Amsterdam, The Netherlands.
Judith Potjewijd *Department of Internal Medicine, Division Nephrology and Clinical Immunology, Maastricht UMC, Maastricht, The Netherlands.
Abraham Rutgers *Department of Rheumatology and Clinical Immunology, UMC Groningen, Groningen, The Netherlands.
Hetty Jolink *Department of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Frank L van de Veerdonk *Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Marit J van Gils *Department of Medical Microbiology and Infection Prevention, Amsterdam Institute for Infection and Immunity, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Rory D de Vries *Department of Viroscience, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Virgil A S H Dalm *Department of Internal Medicine, Division of Allergy & Clinical Immunology, Erasmus MC University Medical Center Rotterdam, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands. v.dalm@erasmusmc.nl.ORCID 0000-0001-5945-4435
VACOPID Research Group
Amsterdam University Medical Centers · NLErasmus MC · NLMaastricht University Medical Centre · NLLeiden University Medical Center · NLUniversity Medical Center Groningen · NLUtrecht University · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatients with inborn errors of immunity (IEI) are at increased risk of severe coronavirus disease-2019 (COVID-19). Effective long-term protection against COVID-19 is therefore of great importance in these patients, but little is known about the decay of the immune response after primary vaccination. We studied the immune responses 6 months after two mRNA-1273 COVID-19 vaccines in 473 IEI patients and subsequently the response to a third mRNA COVID-19 vaccine in 50 patients with common variable immunodeficiency (CVID).

methodsIn a prospective multicenter study, 473 IEI patients (including X-linked agammaglobulinemia (XLA) (N = 18), combined immunodeficiency (CID) (N = 22), CVID (N = 203), isolated or undefined antibody deficiencies (N = 204), and phagocyte defects (N = 16)), and 179 controls were included and followed up to 6 months after two doses of the mRNA-1273 COVID-19 vaccine. Additionally, samples were collected from 50 CVID patients who received a third vaccine 6 months after primary vaccination through the national vaccination program. SARS-CoV-2-specific IgG titers, neutralizing antibodies, and T cell responses were assessed.

resultsAt 6 months after vaccination, the geometric mean antibody titers (GMT) declined in both IEI patients and healthy controls, when compared to GMT 28 days after vaccination. The trajectory of this decline did not differ between controls and most IEI cohorts; however, antibody titers in CID, CVID, and isolated antibody deficiency patients more often dropped to below the responder cut-off compared to controls. Specific T cell responses were still detectable in 77% of controls and 68% of IEI patients at 6 months post vaccination. A third mRNA vaccine resulted in an antibody response in only two out of 30 CVID patients that did not seroconvert after two mRNA vaccines.

conclusionA similar decline in IgG titers and T cell responses was observed in patients with IEI when compared to healthy controls 6 months after mRNA-1273 COVID-19 vaccination. The limited beneficial benefit of a third mRNA COVID-19 vaccine in previous non-responder CVID patients implicates that other protective strategies are needed for these vulnerable patients.

Indexed as

Common Variable ImmunodeficiencyCOVID-19Primary Immunodeficiency Diseases2019-nCoV Vaccine mRNA-1273Antibodies, ViralCOVID-19 VaccinesHumansImmunityImmunoglobulin GProspective StudiesRNA, MessengerSARS-CoV-2Vaccination2019-nCoV Vaccine mRNA-1273Antibodies, ViralCOVID-19 VaccinesImmunoglobulin GRNA, Messengerantibody responseimmunogenicityInborn errors of immunitymRNA-1273 COVID-19 vaccineprimary immunodeficiency disordersSARS-CoV-2T cell response

Identifiers

PMID37231290
PMCPMC10212732
OpenAlexW4378188572

What OpenQuestion holds

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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.