Evidence map›Paper›PMID 40069636›Full record

ArticleBMC infectious diseases2025

Incidence of dynamic seroconversion in subjects received the first dose of the SARS-COV-2 vaccine (AstraZeneca, Moderna and Pfizer) in Kinshasa, Democratic Republic of Congo: prospective cohort study.

Eric Kasongo Mukenge, Blaise Matondo-Manzambi Sumbu, Aliocha Natuhoyila Nkodila, Jeremie Masidi Muwonga, Jean-Robert Rissassi Makulo, Mamy Zita Ngole, Ben Izizag Bepouka, Murielle Mashi Longokolo, Guyguy Kamwiziku, Hippolyte Nanituma Situakibanza and 13 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Eric Kasongo MukengeDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Blaise Matondo-Manzambi SumbuDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Aliocha Natuhoyila NkodilaDepartment of Family Medicine and Primary Health Care, Protestant University of Congo, Kinshasa, Democratic Republic of Congo. nkodilaaliocha@gmail.com.
Jeremie Masidi MuwongaDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Jean-Robert Rissassi MakuloDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Mamy Zita NgoleDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Ben Izizag BepoukaDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Murielle Mashi LongokoloDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Guyguy KamwizikuDepartment of Microbiology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Hippolyte Nanituma SituakibanzaDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Jean-Marie Ntumba KayembeDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Benjamin Longo-MbenzaDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
George Lelo MvumbiDepartment of Basic Sciences, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Baudouin Buassa-Bu-TsumbuDepartment of Basic Sciences, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Jean Claude MakangaraDepartment of Microbiology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Désire Kulimba MashindaSchool of Public Health, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Eric Musalu MafutaSchool of Public Health, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Donatien Sonzi MangalaDepartment of Internal Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Mireille Nganga NkangaDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Gustave Ntita IlungaDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Fonce Tshibawu NkundaDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Christian Nsimba LengoDepartment of Clinical Biology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Steve Mundeke AhukaDepartment of Microbiology, University of Kinshasa, Kinshasa, Democratic Republic of Congo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMass vaccination efforts worldwide have reduced the incidence of COVID-19, but despite this reduction, seroconversion studies in sub-Saharan Africa are limited. The aim of this study is to assess the incidence of seroconversion in subjects who received the first dose of SARS-COV-2 vaccine (AstraZeneca, Moderna and Pfizer) in Kinshasa.

methodsThis was a prospective study recruiting 918 subjects vaccinated at the Cliniques Universitaires de Kinshasa between 19 April and 14 August 2021. Sociodemographic, haematological, biochemical and serological data were collected. Cox proportional hazards were used to identify predictors of seroconversion with a threshold of p < 0.05.

resultsOf the 918 vaccinated individuals, 69.3% were men with a mean age of 47.4 ± 16.0 years. The incidence of seroconversion at last follow-up was 3.00 per 100 P-D. Patients receiving Pfizer (aRR: 3.19; 95% CI: 2.62-3.88) and Modern (aRR: 1.91; 95% CI: 1.60-2.29) vaccines, men (aRR: 2.03; 95% CI: 1.89-3.20), those with comorbidities (aRR: 2.38; 95% CI: 1.89-3.21); subjects with normal creatinine (aRR: 2.08; 95% CI: 1.88-3.32) and normal ALT (aRR: 3.04; 95% CI: 1.89-4.22) were the factors independently predicting seroconversion.

conclusionThe vaccines used had conferred significant immunity on subjects upon receipt of the first dose. This immunity appears to be greater when using the mRNA vaccine than when using the inactivated vaccine.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2SeroconversionAdultAgedAntibodies, ViralDemocratic Republic of the CongoFemaleHumansIncidenceMaleMiddle AgedProspective StudiesAntibodies, ViralCOVID-19 VaccinesCOVID-19 vaccineDemocratic Republic of CongoIgGSeroconversion

Identifiers

PMID40069636
PMCPMC11899428

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.