2026-06-28T10:36:08Zhttps://docta.ucm.es/rest/oai/request
oai:docta.ucm.es:20.500.14352/1160122025-03-14T18:02:40Zcom_20.500.14352_14col_20.500.14352_15
Docta Complutense author Ascaso del Río, Ana author García Pérez, Javier author Pérez Olmeda, Mayte author Arana Arri, Eunate author Vergara, Itziar author Pérez Ingidua, Carla author Bermejo, Mercedes author Castillo de la Osa, María author Imaz Ayo, Natale author Riaño Fernández, Ioana author Astasio González, Oliver author Díez Fuertes, Francisco author Mejide, Susana author Arrizabalaga, Julio author Hernández Gutiérrez, Lourdes author De la Torre Tarazona, Humberto Erick author Lázaro, Alberto Mariano author Vargas Castrillón, Emilio author Alcamí, José author Portolés Pérez, Antonio 2025-01-24T11:23:32Z 2025-01-24T11:23:32Z 2022-07-01 Ascaso-Del-Rio A, García-Pérez J, Pérez-Olmeda M, Arana-Arri E, Vergara I, Pérez-Ingidua C, Bermejo M, Castillo de la Osa M, Imaz-Ayo N, Riaño Fernández I, et al. Immune response and reactogenicity after immunization with two-doses of an experimental COVID-19 vaccine (CVnCOV) followed by a third-fourth shot with a standard mRNA vaccine (BNT162b2): RescueVacs multicenter cohort study. EClinicalmedicine, 51 (2022), p. 101542, ISSN 2589-5370. https://doi.org/10.1016/j.eclinm.2022.101542. 2589-5370 10.1016/j.eclinm.2022.101542 https://hdl.handle.net/20.500.14352/116012 https://doi.org/10.1016/j.eclinm.2022.101542 https://www.sciencedirect.com/science/article/pii/S2589537022002723?via%3Dihub Background There is no evidence to date on immunogenic response among individuals who participated in clinical trials of COVID-19 experimental vaccines redirected to standard national vaccination regimens. Methods This multicentre, prospective controlled cohort study included subjects who received a COVID-19 experimental vaccine (CVnCoV)(test group, TG) - and unvaccinated subjects (control group, CG), selected among individuals to be vaccinated according to the Spanish vaccination program. All study subjects received BNT162b2 as a standard national vaccination schedule, except 8 (from CG) who received mRNA-1273 and were excluded from immunogenicity analyses. Anti-RBD antibodies level and neutralising titres (NT50) against G614, Beta, Mu, Delta and Omicron variants were analysed. Reactogenicity was also assessed. Findings 130 participants (TG:92; CG:38) completed standard vaccination. In TG, median (IQR) of anti-RBD antibodies after first BNT162b2 dose were 10740¢0 BAU/mL (4466¢0-12500) compared to 29¢8 BAU/mL (14¢5-47¢8) in CG (p <0¢0001). Median NT50 (IQR) of G614 was 2674¢0 (1865¢0-3997¢0) in TG and 63¢0 (16¢0-123¢1) in CG (p <0¢0001). After second BNT162b2 dose, anti-RBD levels increased to ≥12500 BAU/mL (11625¢0-12500) in TG compared to 1859¢0 BAU/mL (915¢4-3820¢0) in CG (p <0¢0001). NT50 was 2626¢5 (1756¢0-5472¢0) and 850¢4 (525¢ 1-1608¢0), respectively (p <0¢0001). Variant-specific (Beta, Mu, Omicron) response was also assessed. Most frequent adverse reactions were headache, myalgia, and local pain. No severe AEs were reported. Interpretation Heterologous BNT162b2 as third and fourth doses in previously suboptimal immunized individuals elicit stronger immune response than that obtained with two doses of BNT162b2. This apparent benefit was also observed in variant-specific response. No safety concerns arose eng Attribution 4.0 International Immune response and reactogenicity after immunization with two-doses of an experimental COVID-19 vaccine (CVnCOV) followed by a third-fourth shot with a standard mRNA vaccine (BNT162b2): RescueVacs multicenter cohort study. journal article 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URL https://docta.ucm.es/bitstreams/741e1398-29a0-496b-bc1e-4d1916f647d7/download File MD5 ffbdf097ed0696068e3c86353adfc86b 1075650 application/pdf Immune response and reactogenicity.pdf