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巴西的黄热病疫苗接种:青少年自身免疫性风湿病的短期安全性和免疫原性

Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases.

作者信息

Emi Aikawa Nádia, Andrade Balbi Verena, Borba Eduardo Ferreira, Coracini Tonacio Adriana, Maluf Elias Sallum Adriana, Maria Arruda Campos Lucia, Tomie Kozu Kátia, Borges Vendramini Margarete, Fontoura Nicole, de Souza Azevedo Adriana, Dias Schwarcz Waleska, Marli Christovam Sartori Ana, Antonangelo Leila, Artur Silva Clovis, Bonfá Eloisa

机构信息

Pediatric Rheumatology Unit, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, SP, Brazil.

Division of Rheumatology, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, SP, Brazil.

出版信息

Vaccine X. 2021 Dec 10;10:100131. doi: 10.1016/j.jvacx.2021.100131. eCollection 2022 Apr.

Abstract

Yellow fever vaccine (YFV) is a live attenuated vaccine usually contraindicated for juvenile autoimmune rheumatic disease (JARD) patients. During the recent epidemic in Sao Paulo-Brazil, YFV was indicated for patients under low immunosuppression. Thirty JARD patients with inactive diseases undergoing low immunosuppression and 30 healthy controls (HC) were vaccinated with a fractional dose 17DD YFV (∼5495 IU) and evaluated 30 days later. JARD patients and controls had comparable median age (12.4 vs. 12 years, p = 0.250). Disease parameters remained stable 30 days after 17DD YFV (p > 0.05) and only mild adverse events were reported in both groups (p > 0.05). JARD and HC had similar seroprotection [93% vs. 100%;p = 0.49], seroconversion rates [96% vs. 100%;p = 0.489], and GMT [1249 vs.1293;p = 0.821]. Both groups had similar white-blood-cells kinetics with transient decreases in lymphocytes at D5 and neutrophils at D10, followed by full recovery at D30 (P < 0.05). In conclusion, 17DD YFV was safe and immunogenic in JARD. This study may contribute to recommendations for patients living/travelling to endemic areas.

摘要

黄热病疫苗(YFV)是一种减毒活疫苗,通常对青少年自身免疫性风湿病(JARD)患者禁用。在巴西圣保罗最近的疫情期间,YFV被用于低免疫抑制的患者。30例处于疾病缓解期且接受低免疫抑制治疗的JARD患者和30名健康对照(HC)接种了17DD YFV的分剂量(约5495国际单位),并在30天后进行评估。JARD患者和对照组的年龄中位数相当(12.4岁对12岁,p = 0.250)。17DD YFV接种30天后疾病参数保持稳定(p>0.05),两组均仅报告了轻微不良事件(p>0.05)。JARD组和HC组的血清保护率[93%对100%;p = 0.49]、血清转化率[96%对100%;p = 0.489]和几何平均滴度[1249对1293;p = 0.821]相似。两组的白细胞动力学相似,在第5天淋巴细胞短暂减少,第10天中性粒细胞短暂减少,随后在第30天完全恢复(P<0.05)。总之,17DD YFV在JARD患者中是安全且具有免疫原性的。本研究可能有助于为生活在/前往疫区的患者提供建议。

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