羟氯喹与原发性斯约格伦综合征患者接种 17DD 黄热病初免疫苗后较低的血清转换率有关。

IF 4.1 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Human Vaccines & Immunotherapeutics Pub Date : 2024-12-31 Epub Date: 2024-07-03 DOI:10.1080/21645515.2024.2318814
Ketty Lysie Libardi Lira Machado, Ismael Artur da Costa-Rocha, Laura Gonçalves Rodrigues Aguiar, Isac Ribeiro Moulaz, Samira Tatiyama Miyamoto, Priscila Costa Martins, Erica Vieira Serrano, Ana Paula Espíndula Gianordoli, Maria da Penha Gomes Gouvea, Maria de Fatima Bissoli, Sheila Maria Barbosa de Lima, Waleska Dias Schwarcz, Adriana de Souza Azevedo, Juliana Fernandes Amorim da Silva, Renata Tourinho Santos, Joaquim Pedro Brito-de-Sousa, Jordana Grazziela Coelho-Dos-Reis, Ana Carolina Campi-Azevedo, Andréa Teixeira-Carvalho, Vanessa Peruhype-Magalhães, Francieli Fontana Sutile Tardetti Fantinato, Licia Maria Henrique da Mota, Olindo Assis Martins-Filho, Valéria Valim
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引用次数: 0

摘要

本研究旨在探讨原发性斯约格伦综合征(pSS)患者计划接种17DD-黄热病(YF)初代疫苗(Bio-Manguinhos-FIOCRUZ)后,羟氯喹(HCQ)治疗是否会影响中和抗体的产生、病毒血症水平以及血清可溶性介质的动力学。共招募了 34 名原发性斯约格伦综合征(pSS)患者和 23 名健康对照组(HC)。根据是否使用 HCQ(HCQ 和非 HCQ)对 pSS 组进行了进一步分类。在基线和随后的时间点(第0天/第3天-第4天/第5天-第6天/第7天/第14天-第D28天)进行了YF-斑块还原中和试验(PRNT≥1:50)、YF病毒血症(RNAnemia)和血清生物标志物分析。pSS 组的 PRNT 滴度和血清阳性率与 HC 组相似(GeoMean = 238 vs 440,p = .11;82% vs 96%,p = .13)。然而,HCQ 亚组的血清转换率低于 HC(GeoMean = 161 vs 440,p = .04;69% vs 96%,p = .02)和非 HCQC(GeoMean = 161 vs 337,p = .582;69% vs 94%,p = .049)。亚组之间的 YF 病毒血症没有差异。血清生物标志物分析表明,HCQ 亚组的 CCL2、CXL10、IL-6、IFN-γ、IL1-Ra、IL-9、IL-10 和 IL-2 水平在基线时有所升高,并且在动力学时间轴上的多个生物标志物水平持续升高,直至 D14-28。这些结果表明,与非羟基氯喹亚组相比,羟基氯喹亚组在17DD-YF初免引起的YF特异性免疫应答中表现出不足。我们的研究结果表明,羟氯喹与 17DD-YF 初免后体液免疫反应的降低有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydroxychloroquine is associated with lower seroconversion upon 17DD-Yellow fever primovaccination in patients with primary Sjögren's syndrome.

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.

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来源期刊
Human Vaccines & Immunotherapeutics
Human Vaccines & Immunotherapeutics BIOTECHNOLOGY & APPLIED MICROBIOLOGY-IMMUNOLOGY
CiteScore
7.90
自引率
8.30%
发文量
489
审稿时长
3-6 weeks
期刊介绍: (formerly Human Vaccines; issn 1554-8619) Vaccine research and development is extending its reach beyond the prevention of bacterial or viral diseases. There are experimental vaccines for immunotherapeutic purposes and for applications outside of infectious diseases, in diverse fields such as cancer, autoimmunity, allergy, Alzheimer’s and addiction. Many of these vaccines and immunotherapeutics should become available in the next two decades, with consequent benefit for human health. Continued advancement in this field will benefit from a forum that can (A) help to promote interest by keeping investigators updated, and (B) enable an exchange of ideas regarding the latest progress in the many topics pertaining to vaccines and immunotherapeutics. Human Vaccines & Immunotherapeutics provides such a forum. It is published monthly in a format that is accessible to a wide international audience in the academic, industrial and public sectors.
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