Evidence map›Paper›PMID 37808936›Full record

ArticleLancet regional health. Americas2023

Protection of homologous and heterologous boosters after primary schemes of rAd26-rAd5, ChAdOx1 nCoV-19 and BBIBP-CorV during the omicron outbreak in adults of 50 years and older in Argentina: a test-negative case-control study.

Soledad González, Santiago Olszevicki, Alejandra Gaiano, Martín Salazar, Lorena Regairaz, Ana Nina Varela Baino, Erika Bartel, Teresa Varela, Veronica V González Martínez, Santiago Pesci and 7 more

Open access · goldAbstract read
In one paragraph

Article in Lancet regional health. Americas, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

17 authors at 4 institutions in 1 country.

Soledad GonzálezMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Santiago OlszevickiMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Alejandra GaianoMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Martín SalazarFaculty of Medical Sciences, National University of La Plata, Argentina.
Lorena RegairazImmunology Unit, Children's Hospital Sor Maria Ludovica, La Plata, Buenos Aires.
Ana Nina Varela BainoMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Erika BartelMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Teresa VarelaMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Veronica V González MartínezMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Santiago PesciMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Lupe MarínMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Juan Ignacio IrassarMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Leticia CerianiMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Enio GarciaMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Nicolás KreplakMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Elisa EstenssoroMinistry of Health of the Province of Buenos Aires, La Plata, Buenos Aires, Argentina.
Franco MarsicoFaculty of Exacts and Natural Sciences, University of Buenos Aires, Argentina.
Ministerio de Salud - Provincia de Buenos Aires · ARHospital de Niños Superiora Sor María Ludovica · ARUniversidad de Buenos Aires · ARUniversidad Nacional de La Plata · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: After primary vaccination schemes with rAd26-rAd5 (Sputnik V), ChAdOx1 nCoV-19, BBIBP-CorV or heterologous combinations, the effectiveness of homologous or heterologous boosters (Sputnik V, ChAdOx, Pfizer-BioNTech, Moderna) against SARS-CoV-2 infections, hospitalisations and deaths has been scarcely studied. Methods: Test-negative, case-control study, conducted in Argentina during omicron BA.1 predominance, in adults ≥50 years old tested for SARS-CoV-2 who had received two or three doses of COVID-19 vaccines. Outcomes were COVID-associated infections, hospitalisations and deaths after administering mRNA and vectored boosters, < or ≥60 days from the last dose. Findings: Of 422,124 individuals tested for SARS-CoV-2, 221,993 (52.5%) tested positive; 190,884 (45.2%) and 231,260 (54.8%) had received 2-dose and 3-dose vaccination schemes, respectively. The 3-dose scheme reduced infections, hospitalisations and death (OR 0.81 [0.80-0.83]; 0.28 [0.25-0.32] and 0.25 [0.22-0.28] respectively), but protection dropped after 60 days to 1.04 [1.01-1.06]; 0.52 [0.44-0.61] and 0.38 [0.33-0.45]). Compared with 2-dose-schemes, homologous boosters after primary schemes with vectored-vaccines provided lower protection against infections < and ≥60 days (0.94 [0.92-0.97] and 1.05 [1.01-1.09], respectively) but protected against hospitalisations (0.30 [0.26-0.35]) and deaths (0.29 [0.25-0.33]), decreasing after 60 days (0.59 [0.47-0.74] and 0.51 [0.41-0.64], respectively). Heterologous boosters protected against infections (0.70 [0.68-0.71]) but decreased after 60 days (1.01 [0.98-1.04]) and against hospitalisations and deaths (0.26 [0.22-0.31] and 0.22 [0.18-0.25], respectively), which also decreased after 60 days (0.43 [0.35-0.53] and 0.33 [0.26-0.41], respectively). Heterologous boosters protected against infections when applied <60 days (0.70 [0.68-0.71], p < 0.001), against hospitalisations when applied ≥60 days (0.43 [0.35-0.53], p < 0.01), and against deaths < and ≥60 days (0.22 [0.18-0.25], p < 0.01 and 0.33 [0.26-0.41], p < 0.001). Interpretation: During omicron predominance, heterologous boosters such as viral vectored and mRNA vaccines, following Sputnik V, ChAdOx1, Sinopharm or heterologous primary schemes might provide better protection against death; this effect might last longer in individuals aged ≥50 than homologous boosters. Funding: None.

Indexed as

Vaccination

Identifiers

PMID37808936
PMCPMC10558771
OpenAlexW4387129895

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.