Evidence map›Paper›PMID 38793698›Full record

ArticleVaccines2024

Correlates of Breakthrough SARS-CoV-2 Infections in People with HIV: Results from the CIHR CTN 328 Study.

Cecilia T Costiniuk, Terry Lee, Joel Singer, Yannick Galipeau, Corey Arnold, Marc-André Langlois, Judy Needham, Mohammad-Ali Jenabian, Ann N Burchell, Hasina Samji and 19 more

Abstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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.

Cecilia T CostiniukDivision of Infectious Diseases and Chronic Viral Illness Service, McGill University Health Centre, Royal Victoria Hospital-Glen Site, Montreal, QC H4A 3J1, Canada.ORCID 0000-0002-4547-714X
Terry LeeCIHR Canadian HIV Trials Network (CTN), Vancouver, BC V6Z 1Y6, Canada.
Joel SingerCIHR Canadian HIV Trials Network (CTN), Vancouver, BC V6Z 1Y6, Canada.
Yannick GalipeauDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Corey ArnoldDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Marc-André LangloisDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1N 6N5, Canada.ORCID 0000-0003-4652-3029
Judy NeedhamCIHR Canadian HIV Trials Network (CTN), Vancouver, BC V6Z 1Y6, Canada.
Mohammad-Ali JenabianDepartment of Biological Sciences, Université du Québec à Montréal, Montreal, QC H2X 1Y4, Canada.ORCID 0000-0003-4321-9777
Ann N BurchellDepartment of Family and Community Medicine, St. Michael's Hospital, Unity Health Toronto, Toronto, ON M5B 1W8, Canada.
Hasina SamjiFaculty of Health Sciences, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.
Catharine ChambersDalla Lana School of Public Health, University of Toronto, Toronto, ON M5T 3M7, Canada.
Sharon WalmsleyDivision of Infectious Diseases, Department of Medicine, University of Toronto, Toronto, ON M5S 3H2, Canada.ORCID 0000-0002-3959-5692
Mario OstrowskiClinical Sciences Division, Department of Immunology, Li Ka Shing Knowledge Institute, St. Michael's Hospital, University of Toronto, Toronto, ON M5B 1T8, Canada.
Colin KovacsDivision of Infectious Diseases, Faculty of Medicine, University of Toronto, Toronto, ON M5S 3H2, Canada.
Darrell H S TanMAP Centre for Urban Health Solutions, St. Michael's Hospital, Unity Health Toronto, Toronto, ON M5B 1T8, Canada.ORCID 0000-0002-3069-2875
Marianne HarrisBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, BC V6Z 1Y6, Canada.
Mark HullBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, BC V6Z 1Y6, Canada.
Zabrina L BrummeFaculty of Health Sciences, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.ORCID 0000-0002-8157-1037
Hope R LapointeBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, BC V6Z 1Y6, Canada.ORCID 0000-0002-6847-9156
Mark A BrockmanFaculty of Health Sciences, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.ORCID 0000-0001-6432-1426
Shari MargoleseCIHR Canadian HIV Trials Network (CTN), Vancouver, BC V6Z 1Y6, Canada.
Enrico MandarinoCIHR Canadian HIV Trials Network (CTN), Vancouver, BC V6Z 1Y6, Canada.
Suzanne SamaraniDivision of Infectious Diseases and Chronic Viral Illness Service, McGill University Health Centre, Royal Victoria Hospital-Glen Site, Montreal, QC H4A 3J1, Canada.
Bertrand LebouchéDivision of Infectious Diseases and Chronic Viral Illness Service, McGill University Health Centre, Royal Victoria Hospital-Glen Site, Montreal, QC H4A 3J1, Canada.ORCID 0000-0002-1273-9393
Jonathan B AngelDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Jean-Pierre RoutyDivision of Infectious Diseases and Chronic Viral Illness Service, McGill University Health Centre, Royal Victoria Hospital-Glen Site, Montreal, QC H4A 3J1, Canada.ORCID 0000-0001-9897-7589
Curtis L CooperDivision of Infectious Diseases, Department of Medicine, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON K1H 8L6, Canada.ORCID 0000-0002-3368-3499
Aslam H AnisCIHR Canadian HIV Trials Network (CTN), Vancouver, BC V6Z 1Y6, Canada.ORCID 0000-0003-0323-8885
COVAXHIV Study Group

Funding

CIHR N/APublic Health Agency of Canada 2122-HQ-000075
6 · The paper itself

Abstract

COVID-19 breakthrough infection (BTI) can occur despite vaccination. Using a multi-centre, prospective, observational Canadian cohort of people with HIV (PWH) receiving ≥2 COVID-19 vaccines, we compared the SARS-CoV-2 spike (S) and receptor-binding domain (RBD)-specific IgG levels 3 and 6 months post second dose, as well as 1 month post third dose, in PWH with and without BTI. BTI was defined as positivity based on self-report measures (data up to last study visit) or IgG data (up to 1 month post dose 3). The self-report measures were based on their symptoms and either a positive PCR or rapid antigen test. The analysis was restricted to persons without previous COVID-19 infection. Persons without BTI remained COVID-19-naïve until ≥3 months following the third dose. Of 289 participants, 92 developed BTI (31.5 infections per 100 person-years). The median days between last vaccination and BTI was 128 (IQR 67, 176), with the most cases occurring between the third and fourth dose (n = 59), corresponding to the Omicron wave. In analyses adjusted for age, sex, race, multimorbidity, hypertension, chronic kidney disease, diabetes and obesity, a lower IgG S/RBD (log10 BAU/mL) at 1 month post dose 3 was significantly associated with BTI, suggesting that a lower IgG level at this time point may predict BTI in this cohort of PWH.

Indexed as

breakthrough infectionCOVID-19 vaccinationHIVhumoral immunityimmunogenicityimmunosuppressed hostsSARS-CoV-2

Identifiers

PMID38793698
PMCPMC11125718

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.