Evidence map›Paper›PMID 42022223›Full record

ArticleThe journal of allergy and clinical immunology. Global2026

Four doses of coronavirus disease 2019 vaccination for patients with inborn errors of immunity compared to 3 doses for healthy individuals.

Jeffery C H Chan, Samuel M S Cheng, Daniel Leung, Xiwei Wang, Manni Wang, Yin Celeste Cheuk, Cyrus Ho, Leo C H Tsang, Tsz Chun Kwan, Amos M T Lee and 10 more

Registry-linked trialAbstract read
In one paragraph

Article in The journal of allergy and clinical immunology. Global, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04800133 (To Compare the Reactogenicity and Immunogenicity of Recommended COVID-19 Vaccines in Young Adolescents and Children in Hong Kong), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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.

NCT04800133 phase2unknown statusnot on this map

To Compare the Reactogenicity and Immunogenicity of Recommended COVID-19 Vaccines in Young Adolescents and Children in Hong Kong

TypeinterventionalSponsorThe University of Hong KongRan2021 to 2025Enrolled1,018ConditionsCovid19ArmsTozinameran, CoronaVac, CoronaVac, intradermal
3 · Its place in the literature

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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

20 authors.

Jeffery C H ChanDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Samuel M S ChengSchool of Public Health, The University of Hong Kong, Hong Kong.
Daniel LeungDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Xiwei WangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Manni WangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Yin Celeste CheukDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Cyrus HoDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Leo C H TsangSchool of Public Health, The University of Hong Kong, Hong Kong.
Tsz Chun KwanSchool of Public Health, The University of Hong Kong, Hong Kong.
Amos M T LeeDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Wing Yan LiDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Jennifer H Y LamDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Kaiyue ZhangDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Issan Y S TamDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Sau Man ChanDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Koon Wing ChanDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Malik PeirisSchool of Public Health, The University of Hong Kong, Hong Kong.
Wenwei TuDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Yu Lung LauDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.
Jaime S Rosa DuqueDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with inborn errors of immunity (IEI) have high risks of severe complications after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Although vaccination is effective in preventing severe coronavirus disease 2019 (COVID-19), boosters are required as the protection provided wanes over time. A greater number of boosters may be required in IEI patients compared to healthy individuals because of their immunodeficient state, but no such data are available. Objective: We investigated and compared the immunogenicity between 4 doses of COVID-19 vaccination for patients with IEI and 3 doses for healthy individuals. Methods: In the current study (NCT04800133), either BNT162b2 or CoronaVac was administered as dose 4. Healthy individuals who received 3 doses were included for comparison. Humoral and cellular immunogenicity against wild-type and JN.1 SARS-CoV-2 was assessed between IEI patients and healthy individuals. Results: IEI patients had lower humoral and cellular immunogenicity than healthy individuals after 3 doses of COVID-19 vaccination. After dose 4, IEI patients obtained immunogenicity similar to that of healthy individuals who received 3 doses. A fourth dose of BNT162b2 significantly enhanced humoral and cellular immunogenicity against wild-type SARS-CoV-2 and humoral responses against JN.1 SARS-CoV-2. In contrast, CoronaVac had minimal effect on humoral responses to wild-type and JN.1 SARS-CoV-2. Six patients experienced breakthrough infections, which did not result in hospitalization or death. Conclusion: A fourth dose of BNT162b2 was immunogenic and safe for most IEI patients. The fourth dose of vaccination is recommended for IEI patients to improve protection against COVID-19, particularly before travel to areas with high endemic transmission.

Indexed as

COVID-19inborn errors of immunityvaccine

Identifiers

PMID42022223
PMCPMC13098406

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Registered trials

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.