Evidence map›Paper›PMID 35543372›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Antibody Response of Heterologous vs Homologous Messenger RNA Vaccine Boosters Against the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant: Interim Results from the PRIBIVAC Study, a Randomized Clinical Trial.

Xuan Ying Poh, Chee Wah Tan, I Russel Lee, Jean-Marc Chavatte, Siew-Wai Fong, Tessa Prince, Catherine Hartley, Aileen Y Y Yeoh, Suma Rao, Po Ying Chia and 16 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. 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 25 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 3 pooled it
4.2field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 3 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  5. Variant-Specific IgA Protects Against Omicron Infection.The Journal of infectious diseases · 2024
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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

26 authors at 6 institutions in 2 countries.

Xuan Ying PohNational Centre for Infectious Diseases, Singapore, Singapore.ORCID 0000-0001-6077-0515
Chee Wah TanEmerging Infectious Diseases Programme, Duke-National University of Singapore Medical School, Singapore, Singapore.
I Russel LeeNational Centre for Infectious Diseases, Singapore, Singapore.
Jean-Marc ChavatteNational Centre for Infectious Diseases, Singapore, Singapore.
Siew-Wai FongA*STAR Infectious Diseases Lab, Agency for Science Technology and Research, Singapore, Singapore.
Tessa PrinceDepartment of Infection Biology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Catherine HartleyDepartment of Infection Biology, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Aileen Y Y YeohEmerging Infectious Diseases Programme, Duke-National University of Singapore Medical School, Singapore, Singapore.
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.
Sapna P SadaranganiNational Centre for Infectious Diseases, Singapore, Singapore.
Ray J H LinNational Centre for Infectious Diseases, Singapore, Singapore.
Clarissa LimNational Centre for Infectious Diseases, Singapore, Singapore.
Jefanie TeoNational Centre for Infectious Diseases, Singapore, Singapore.
Daniel R X LimNational Centre for Infectious Diseases, Singapore, Singapore.
Wanni ChiaEmerging Infectious Diseases Programme, Duke-National University of Singapore Medical School, Singapore, Singapore.
Julian A HiscoxA*STAR Infectious Diseases Lab, Agency for Science Technology and Research, Singapore, Singapore.
Lisa F P NgA*STAR Infectious Diseases Lab, Agency for Science Technology and Research, Singapore, Singapore.
Ee Chee RenYong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Raymond T P LinNational Centre for Infectious Diseases, Singapore, Singapore.
Laurent ReniaA*STAR Infectious Diseases Lab, Agency for Science Technology and Research, Singapore, Singapore.
David Chien LyeNational Centre for Infectious Diseases, Singapore, Singapore.
Lin-Fa WangEmerging Infectious Diseases Programme, Duke-National University of Singapore Medical School, Singapore, Singapore.
Barnaby E YoungNational Centre for Infectious Diseases, Singapore, Singapore.
National Centre for Infectious Diseases · SGAgency for Science, Technology and Research · SGNational University of Singapore · SGTan Tock Seng Hospital · SGNanyang Technological University · SGUniversity of Liverpool · GB

Funding

Medical Research Council MR/W005611/1
6 · The paper itself

Abstract

backgroundWaning antibody levels post-vaccination and the emergence of variants of concern (VOCs) capable of evading protective immunity have raised the need for booster vaccinations. However, which combination of coronavirus disease 2019 (COVID-19) vaccines offers the strongest immune response against the Omicron variant is unknown.

methodsThis randomized, participant-blinded, controlled trial assessed the reactogenicity and immunogenicity of different COVID-19 vaccine booster combinations. A total of 100 BNT162b2-vaccinated individuals were enrolled and randomized 1:1 to either homologous (BNT162b2 + BNT162b2 + BNT162b2; "BBB") or heterologous messenger RNA (mRNA) (BNT162b2 + BNT162b2 + mRNA-1273; "BBM") booster vaccine. The primary end point was the level of neutralizing antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) wild-type and VOCs at day 28.

resultsA total of 51 participants were allocated to BBB and 49 to BBM; 50 and 48, respectively, were analyzed for safety and immunogenicity outcomes. At day 28 post-boost, mean SARS-CoV-2 spike antibody titers were lower with BBB (22 382 IU/mL; 95% confidence interval [CI], 18 210 to 27 517) vs BBM (29 751 IU/mL; 95% CI, 25 281 to 35 011; P = .034) as was the median level of neutralizing antibodies: BBB 99.0% (interquartile range [IQR], 97.9% to 99.3%) vs BBM 99.3% (IQR, 98.8% to 99.5%; P = .021). On subgroup analysis, significant higher mean spike antibody titer, median surrogate neutralizing antibody level against all VOCs, and live Omicron neutralization titer were observed only in older adults receiving BBM. Both vaccines were well tolerated.

conclusionsHeterologous mRNA-1273 booster vaccination compared with homologous BNT123b2 induced a stronger neutralizing response against the Omicron variant in older individuals. CLINICAL TRIALS REGISTRATION: NCT05142319.

Indexed as

BNT162 VaccineCOVID-192019-nCoV Vaccine mRNA-1273AgedAntibodies, NeutralizingAntibodies, ViralAntibody FormationCOVID-19 VaccinesHumansImmunization, SecondarySARS-CoV-2Vaccination2019-nCoV Vaccine mRNA-1273Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesCOVID-19 vaccine boosterhumoral immunitylive virus neutralizationOmicron

Identifiers

PMID35543372
PMCPMC9129205
OpenAlexW4280558095

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.