Elsevier

Vaccine

Volume 40, Issue 5, 31 January 2022, Pages 811-818
Vaccine

Evaluation of the Gam-COVID-Vac and vaccine-induced neutralizing response against SARS-CoV-2 lineage P.1 variant in an Argentinean cohort

https://doi.org/10.1016/j.vaccine.2021.12.027Get rights and content

Abstract

We evaluated humoral immune-response elicited by Sputnik-V by measuring anti-Spike (S) IgG antibodies (Abs) and neutralizing antibodies (NAb) prior to, 14 and 42 days after-vaccination. The safety and disease rates among vaccinated individuals were also evaluated. Since SARS-CoV-2 lineage P.1 is rapidly spreading in Argentina, virus-neutralizing activity of Sputnik-V-elicited and infection-elicited NAb faced to P.1 were also assessed. A total of 285 participants were recruited; all reported good tolerance, without any severe adverse event. Nine COVID-19 cases were confirmed in fully vaccinated individuals and viable P.1 variant was successfully isolated from one of them. At day 42, 99.65% of the individuals had anti-S IgG; however, 23.15% had not detectable NAbs. Significantly higher neutralization potency against WT compared to P.1 (p < 0·001) was observed. Some samples failed to neutralize P.1, mainly among vaccinated-naїve subjects; however, no significant differences were observed among previously infected-vaccinated individuals. Our results corroborated that Sputnik-V is safe and induces an efficient humoral immune response, although not all immunized subjects develop Nabs. Herein, we show for the first time, evidence of infectious SARS-CoV-2 shedding from Sputnik-V fully vaccinated individuals, by the isolation of viable virus from the nasopharyngeal swab of one participant of our study, 139 days after receiving the second dose. Thereby, we provide evidence indicating that the vaccine might avoid severe forms of COVID-19 but does not prevent infection nor prevents transmission from a fully vaccinated individual.

Keywords

SARS-CoV-2
COVID-19
Sputnik-V
SARS-CoV-2 lineage P.1
Neutralizing antibodies
Variants of concern

Cited by (0)

1

Participants from MinSalCba working group: Hospital Rawson: Alejandra Álvarez, Lorena Ravera, Liliana Zappia, Aldo Barrera, Canela Brarda, Josefina Eynard Asua, Claudia Toledo, Carla Daniela Barrientos Alvarado, Julia Sabbatini, Laura Belén Coletti and Margarita Inés Cáceres;; Laboratorio Central: Gonzalo Manuel Castro.

2

Participants from FCM-UNC working group: Dean Rogelio Pizzi, Silvia Nates, Viviana Ré and Belén Pisano.

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