Hydroxychloroquine is associated with lower seroconversion upon 17DD-Yellow fever primovaccination in patients with primary Sjögren's syndrome.
Ketty Lysie Libardi Lira MachadoIsmael Artur da Costa-RochaLaura Gonçalves Rodrigues AguiarIsac Ribeiro MoulazSamira Tatiyama MiyamotoPriscila Costa MartinsErica Vieira SerranoAna Paula Espíndula GianordoliMaria da Penha Gomes GouveaMaria de Fatima BissoliSheila Maria Barbosa de LimaWaleska Dias SchwarczAdriana de Souza AzevedoJuliana Fernandes Amorim da SilvaRenata Tourinho SantosJoaquim Pedro Brito-de-SousaJordana Grazziela Coelho-Dos-ReisAna Carolina Campi-AzevedoAndréa Teixeira-CarvalhoVanessa Peruhype-MagalhãesFrancieli Fontana Sutile Tardetti FantinatoLicia Maria Henrique da MotaOlindo Assis Martins-FilhoValéria ValimPublished in: Human vaccines & immunotherapeutics (2024)
The present study aimed at investigating whether the hydroxychloroquine (HCQ) treatment would impact the neutralizing antibody production, viremia levels and the kinetics of serum soluble mediators upon planned 17DD-Yellow Fever (YF) primovaccination (Bio-Manguinhos-FIOCRUZ) of primary Sjögren's syndrome (pSS). A total of 34 pSS patients and 23 healthy controls (HC) were enrolled. The pSS group was further categorized according to the use of HCQ (HCQ and Non-HCQ). The YF-plaque reduction neutralization test (PRNT ≥1:50), YF viremia (RNAnemia) and serum biomarkers analyses were performed at baseline and subsequent time-points (Day0/Day3-4/Day5-6/Day7/Day14-D28). The pSS group showed PRNT titers and seropositivity rates similar to those observed for HC (GeoMean = 238 vs 440, p = .11; 82% vs 96%, p = .13). However, the HCQ subgroup exhibited lower seroconversion rates as compared to HC (GeoMean = 161 vs 440, p = .04; 69% vs 96%, p = .02) and Non-HQC (GeoMean = 161 vs 337, p = .582; 69% vs 94%, p = .049). No differences in YF viremia were observed amongst subgroups. Serum biomarkers analyses demonstrated that HCQ subgroup exhibited increased levels of CCL2, CXL10, IL-6, IFN-γ, IL1-Ra, IL-9, IL-10, and IL-2 at baseline and displayed a consistent increase of several biomarkers along the kinetics timeline up to D14-28. These results indicated that HCQ subgroup exhibited a deficiency in assembling YF-specific immune response elicited by 17DD-YF primovaccination as compared to Non-HCQ subgroup. Our findings suggested that hydroxychloroquine is associated with a decrease in the humoral immune response after 17DD-YF primovaccination.