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Do immunosuppressive treatments influence immune responses against adenovirus-based COVID-19 vaccines in patients with multiple sclerosis? An Argentine multicenter study

Authors :
Berenice Anabel Silva
Esteban Miglietta
Juan Cruz Casabona
Shirley Wenker
María Bárbara Eizaguirre
Ricardo Alonso
Magdalena Casas
Luciana Grimanesa Lázaro
Federico Man
Gustavo Portuondo
Abril Lopez Bisso
Noelia Zavala
Federico Casales
Gastón Imhoff
Dra Judith Steinberg
Pablo Adrián López
Edgar Carnero Contentti
Norma Deri
Vladimiro Sinay
Javier Hryb
Edson Chiganer
Felisa Leguizamon
Verónica Tkachuk
Johana Bauer
Flavia Ferrandina
Susana Giachello
Paula Henestroza
Orlando Garcea
Carla Antonela Pascuale
Mauro Heitrich
Osvaldo L. Podhajcer
Sabrina Vinzón
Tomas D’Alotto-Moreno
Alejandro Benatar
Gabriel Adrián Rabinovich
Fernando J. Pitossi
Carina C. Ferrari
Source :
Frontiers in Immunology, Vol 15 (2024)
Publication Year :
2024
Publisher :
Frontiers Media S.A., 2024.

Abstract

IntroductionThere are no reports in LATAM related to longitudinal humoral and cellular response to adenovirus based COVID-19 vaccines in people with Multiple Sclerosis (pwMS) under different disease modifying therapies (DMTs) and neutralization of the Omicron and Wuhan variants of SARS-COV-2.MethodsIgG anti- SARS-COV-2 spike titer were measured in a cohort of 101 pwMS under fingolimod, dimethyl fumarate, cladribine and antiCD20, as well as 28 healthy controls (HC) were measured 6 weeks after vaccination with 2nd dose (Sputnik V or AZD1222) and 3nd dose (homologous or heterologous schedule). Neutralizing capacity was against Omicron (BA.1) and Wuhan (D614G) variants and pseudotyped particles and Cellular response were analyzed.ResultsMultivariate regression analysis showed anti-cd20 (β= -,349, 95% CI: -3655.6 - -369.01, p=0.017) and fingolimod (β=-,399, 95% CI: -3363.8 - -250.9, p=0.023) treatments as an independent factor associated with low antibody response (r2 adjusted=0.157). After the 2nd dose we found a correlation between total and neutralizing titers against D614G (rho=0.6; p

Details

Language :
English
ISSN :
16643224
Volume :
15
Database :
Directory of Open Access Journals
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.972cf15a26444b8b412c6171986b36
Document Type :
article
Full Text :
https://doi.org/10.3389/fimmu.2024.1431403