CONGO | WP2 | |||
Organization | Fondation Congolaise pour la recherche médicale (FCRM) | |||
Name of cohort | Retrospective cross-sectional study on SARS-CoV-2 variant analysis | |||
Referring partner | FCRM | |||
Cohort Information | Country(-ies), cities, regions or centers involved | Republic of Congo, Brazzaville, FCRM | ||
Time of data collection | 03/2020 | 03/2023 | ||
Enrolment | Inactive | |||
Study setting | Multi-centers | |||
Population | Age | Adults,Elderly | ||
Type | Both | |||
Total number of patients | 76 | |||
Site of enrolment (WP2) | Outpatient | |||
Data collection | Clinical data | True | ||
Serological data | True | |||
Genetic data | True | |||
Sample collection | True | |||
Sample collected | Whole blood | No | ||
PBMC | No | |||
Dry-spot blood | No | |||
Plasma | Yes | |||
Serum | No | |||
Stool | No | |||
NP swabs | No | |||
Other | None | |||
Description | The main objective of this project is to assess in people living in Brazzaville who have been vaccinated with Sinopharm 2, Sputnik V or Johnson & Johnson vaccines, the protection provided by these three vaccines; the specific objectives are: - Evaluate the immune response, in particular the humoral response induced by the 3 vaccines, by determining the level and type of antibodies in people vaccinated over 12 months; - Evaluate the number of infections and re-infections in people vaccinated over 12 months - Determine the most suitable vaccine for the study population by comparing the protection indicators according to the vaccine administered The participants in this project are volunteers living in Brazzaville vaccinated and having received the first dose of one of the three (3) vaccines currently used in Congo. They will be included in CCLAM where they will receive essential information, will be registered and will offer a nasopharyngeal swab for RT-PCR screening for sars-cov2, and a blood sample for antibody testing against this virus. These participants will be followed for a period of one year at the rate of four visits: D1 after the first dose and then 14 days, 2 months, 6 months and 12 months after the 2nd dose of vaccines. | |||
Publications |
- Assessment of neutralizing antibody responses after natural SARS-CoV-2 infection and vaccination in Congolese individuals [BMC Infectious Diseases] - Mucosal response of inactivated and recombinant COVID-19 vaccines in Congolese individuals [Immunity, Inflammation and Disease] |