Evidence map›Paper›PMID 35543278›Full record

ArticleThe Journal of infectious diseases2022

Older Adults Mount Less Durable Humoral Responses to Two Doses of COVID-19 mRNA Vaccine but Strong Initial Responses to a Third Dose.

Francis Mwimanzi, Hope R Lapointe, Peter K Cheung, Yurou Sang, Fatima Yaseen, Gisele Umviligihozo, Rebecca Kalikawe, Sneha Datwani, F Harrison Omondi, Laura Burns and 20 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.8field-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.

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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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  18. Challenges in the Vaccination of the Elderly and Strategies for Improvement.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 5 institutions in 1 country.

Francis MwimanziFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Hope R LapointeBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, Canada.
Peter K CheungFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Yurou SangFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Fatima YaseenFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Gisele UmviligihozoFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Rebecca KalikaweFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Sneha DatwaniFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
F Harrison OmondiFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Laura BurnsDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Landon YoungDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Victor LeungDepartment of Medicine, University of British Columbia, Vancouver, Canada.
Olga AgafiteiFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Siobhan EnnisFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Winnie DongBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, Canada.
Simran BasraFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Li Yi LimFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Kurtis NgFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Ralph PantophletFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Chanson J BrummeBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, Canada.
Julio S G MontanerBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, Canada.
Natalie PrystajeckyDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Christopher F LoweDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Mari L DeMarcoDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Daniel T HolmesDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Janet SimonsDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Masahiro NiikuraFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Marc G RomneyDivision of Medical Microbiology and Virology, St Paul's Hospital, Vancouver, Canada.
Zabrina L BrummeFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Mark A BrockmanFaculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
Simon Fraser University · CAAIDS Vancouver · CASt. Paul's Hospital · CAUniversity of British Columbia · CABC Centre for Disease Control · CA

Funding

NIH HHS R01AI134229Wellcome Trust 107752/Z/15/Z)
6 · The paper itself

Abstract

backgroundThird coronavirus disease 2019 (COVID-19) vaccine doses are broadly recommended, but immunogenicity data remain limited, particularly in older adults.

methodsWe measured circulating antibodies against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein receptor-binding domain, ACE2 displacement, and virus neutralization against ancestral and omicron (BA.1) strains from prevaccine up to 1 month following the third dose, in 151 adults aged 24-98 years who received COVID-19 mRNA vaccines.

resultsFollowing 2 vaccine doses, humoral immunity was weaker, less functional, and less durable in older adults, where a higher number of chronic health conditions was a key correlate of weaker responses and poorer durability. One month after the third dose, antibody concentrations and function exceeded post-second-dose levels, and responses in older adults were comparable in magnitude to those in younger adults at this time. Humoral responses against omicron were universally weaker than against the ancestral strain after both the second and third doses. Nevertheless, after 3 doses, anti-omicron responses in older adults reached equivalence to those in younger adults. One month after 3 vaccine doses, the number of chronic health conditions, but not age, was the strongest consistent correlate of weaker humoral responses.

conclusionsResults underscore the immune benefits of third COVID-19 vaccine doses, particularly in older adults.

Indexed as

COVID-19COVID-19 VaccinesAgedAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralHumansmRNA VaccinesRNA, MessengerSARS-CoV-2Spike Glycoprotein, CoronavirusVaccines, SyntheticAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesmRNA VaccinesRNA, MessengerSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, SyntheticACE2 displacementbinding antibodiesCOVID-19humoral immunitymRNAolder adultsomicronSARS-CoV-2vaccineviral neutralization

Identifiers

PMID35543278
PMCPMC9129202
OpenAlexW4280535092

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.