Evidence map›Paper›PMID 37996071›Full record

Trial reportThe Journal of infectious diseases2024

Variant-Specific IgA Protects Against Omicron Infection.

Yun Shan Goh, Siew-Wai Fong, Pei Xiang Hor, Chiew Yee Loh, Bei Wang, Siti Nazihah Mohd Salleh, Eve Zi Xian Ngoh, Raphael Tze Chuen Lee, Xuan Ying Poh, Suma Rao and 19 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IV
In one paragraph

Trial report in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05142319 (Heterologous Prime-boost-boost Vaccine Combinations for Long-term Humoral and Cellular Immunity Against COVID-19), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 38% 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.

NCT05142319 phase4completednot on this map

Heterologous Prime-boost-boost Vaccine Combinations for Long-term Humoral and Cellular Immunity Against COVID-19

TypeinterventionalSponsorTan Tock Seng HospitalRan2021 to 2024Enrolled326ConditionsCOVID-19ArmsHomologous mRNA booster vaccine, Heterologous mRNA booster vaccine, COVAXIN, Nuvaxovid
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

29 authors at 8 institutions in 3 countries.

Yun Shan GohA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Siew-Wai FongA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Pei Xiang HorA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Chiew Yee LohA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Bei WangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Siti Nazihah Mohd SallehSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Eve Zi Xian NgohSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Raphael Tze Chuen LeeBioinformatics Institute, Agency for Science, Technology and Research, Singapore, Singapore.
Xuan Ying PohNational Centre for Infectious Diseases, Singapore, Singapore.ORCID 0000-0001-6077-0515
Suma RaoNational Centre for Infectious Diseases, Singapore, Singapore.
Po Ying ChiaNational Centre for Infectious Diseases, Singapore, Singapore.
Sean W X OngNational Centre for Infectious Diseases, Singapore, Singapore.
Tau Hong LeeNational Centre for Infectious Diseases, Singapore, Singapore.
Clarissa LimNational Centre for Infectious Diseases, Singapore, Singapore.
Jefanie TeoNational Centre for Infectious Diseases, Singapore, Singapore.
Surinder PadaDivision of Infectious Diseases, Ng Teng Fong General Hospital, Singapore, Singapore.
Louisa Jin SunInfectious Diseases, Alexandra Hospital, Singapore, Singapore.
Desmond Luan Seng OngNational University Polyclinic, Singapore, Singapore.
Jyoti SomaniDivision of Infectious Diseases, Department of Medicine, National University Hospital, National University Health System, Singapore, Singapore.
Eng Sing LeeLee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
Sebastian Maurer-StrohA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.ORCID 0000-0003-0813-9640
Cheng-I WangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Yee-Sin LeoNational Centre for Infectious Diseases, Singapore, Singapore.
David C LyeNational Centre for Infectious Diseases, Singapore, Singapore.ORCID 0000-0003-0324-0205
Barnaby Edward YoungNational Centre for Infectious Diseases, Singapore, Singapore.
Lisa F P NgA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Laurent ReniaA*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.ORCID 0000-0003-0349-1557
NCID Study Group
COVID-19 Cohort Study Group
Agency for Science, Technology and Research · SGNanyang Technological University · SGNational Centre for Infectious Diseases · SGNational University of Singapore · SGTan Tock Seng Hospital · SGAlexandra Hospital · SGNational University Hospital · SGNg Teng Fong General Hospital · SG

Funding

Agency for Science, Technology and Research ACCL/19-GAP064-R20H-HBiomedical ResearchCouncilNanyang Technological UniversityNational Medical Research CouncilSingaporeSingapore COVID19RF-001TF IPC, LtdUS Food and Drug Administration 75F40120C00085
6 · The paper itself

Abstract

backgroundThe emergence of rapidly evolving severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, coupled with waning vaccine-induced immunity, has contributed to the rise of vaccine breakthrough infections. It is crucial to understand how vaccine-induced protection is mediated.

methodsWe examined 2 prospective cohorts of mRNA vaccinated and boosted individuals during the Omicron wave of infection in Singapore.

resultsWe found that individuals who remain uninfected over the follow-up period had a higher variant-specific IgA, but not IgG, antibody response at 1 month after booster vaccination, compared with individuals who became infected.

conclusionsWe conclude that IgA may have a potential contributory role in protection against Omicron infection. Clinical Trials Registration . NCT05142319.

Indexed as

Antibodies, ViralCOVID-19COVID-19 VaccinesImmunoglobulin ASARS-CoV-2AdultFemaleHumansImmunization, SecondaryImmunoglobulin GMaleMiddle AgedProspective StudiesSingaporeVaccinationAntibodies, ViralCOVID-19 VaccinesImmunoglobulin AImmunoglobulin GantibodiesCOVID-19IgAmRNA vaccineOmicronSARS-CoV-2S protein

Identifiers

PMID37996071
PMCPMC11326848
OpenAlexW4388982232

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.