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自身免疫性炎性风湿病(pedAIIRD)患儿接种疫苗的疗效、免疫原性和安全性:欧洲抗风湿病联盟(EULAR)/儿科风湿病学会(PRES)2021年更新建议的系统文献综述

Efficacy, Immunogenicity and Safety of Vaccination in Pediatric Patients With Autoimmune Inflammatory Rheumatic Diseases (pedAIIRD): A Systematic Literature Review for the 2021 Update of the EULAR/PRES Recommendations.

作者信息

Jansen Marc H, Rondaan Christien, Legger Geertje, Minden Kirsten, Uziel Yosef, Toplak Nataša, Maritsi Despoina, van den Berg Mirjam, Berbers Guy, Bruijning Patricia, Egert Yona, Normand Christophe, Bijl Marc, Foster Helen, Kone-Paut Isabelle, Wouters Carine, Ravelli Angelo, Elkayam Ori, Wulffraat Nicolaas M, Heijstek Marloes W

机构信息

Department of Paediatric Immunology & Rheumatology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, Netherlands.

RITA, European Reference Networks, Brussels, Belgium.

出版信息

Front Pediatr. 2022 Jul 6;10:910026. doi: 10.3389/fped.2022.910026. eCollection 2022.

Abstract

BACKGROUND

In 2011, the first European League Against Rheumatism (EULAR) vaccination recommendations for pediatric patients with autoimmune inflammatory rheumatic diseases (pedAIIRD) were published. The past decade numerous new studies were performed to assess the safety, efficacy and immunogenicity of vaccinations in pedAIIRD. A systematic literature review (SLR) was therefore performed to serve as the basis for the updated 2021 EULAR/PRES recommendations.

METHODS

An SLR was performed according to the standard operating procedures for EULAR-endorsed recommendations. Primary outcomes were efficacy, immunogenicity and safety of vaccination in pedAIIRD. The search was performed in Medline, Embase and the Cochrane Library and included studies published from November 2010 until July 2020.

RESULTS

The SLR yielded 57 studies which were included for critical appraisal and data extraction. Only 8 studies described the occurrence of vaccine-preventable infections after vaccination (efficacy), none of these studies were powered to assess efficacy. The majority of studies assessed (humoral) immune responses as surrogate endpoint for vaccine efficacy. Studies on non-live vaccines showed that these were safe and in general immunogenic. Biologic disease-modifying antirheumatic drugs (bDMARDs) in general did not significantly reduce seroprotection rates, except for B-cell depleting therapies which severely hampered humoral responses. Four new studies on human papilloma virus vaccination showed that this vaccine was safe and immunogenic in pedAIIRD. Regarding live-attenuated vaccinations, level 1 evidence of the measles mumps rubella (MMR) booster vaccination became available which showed the safety of this booster for patients treated with methotrexate. In addition, level 3 evidence became available that suggested that the MMR and varicella zoster virus (VZV) vaccination for patients on low dose glucocorticosteroids and bDMARDs might be safe as well.

CONCLUSIONS

The past decade, knowledge on the safety and immunogenicity of (live-attenuated) vaccines in pedAIIRD significantly increased. Data on efficacy (infection prevention) remains scarce. The results from this SLR are the basis for the updated EULAR/PRES vaccination recommendations in pedAIIRD.

摘要

背景

2011年,欧洲抗风湿病联盟(EULAR)首次发布了针对儿童自身免疫性炎症性风湿病(pedAIIRD)患者的疫苗接种建议。在过去十年中,开展了大量新研究以评估pedAIIRD患者接种疫苗的安全性、有效性和免疫原性。因此,进行了一项系统文献综述(SLR),作为2021年EULAR/PRES更新建议的基础。

方法

根据EULAR认可的建议的标准操作程序进行SLR。主要结局是pedAIIRD患者接种疫苗的有效性、免疫原性和安全性。检索在Medline、Embase和Cochrane图书馆进行,纳入2010年11月至2020年7月发表的研究。

结果

SLR产生了57项研究,纳入进行严格评价和数据提取。只有8项研究描述了接种疫苗后疫苗可预防感染的发生情况(有效性),这些研究均无足够效力评估有效性。大多数研究将(体液)免疫反应作为疫苗有效性的替代终点进行评估。关于非活疫苗的研究表明,这些疫苗是安全的,且一般具有免疫原性。除了严重阻碍体液反应的B细胞耗竭疗法外,生物性改善病情抗风湿药物(bDMARDs)一般不会显著降低血清保护率。四项关于人乳头瘤病毒疫苗接种的新研究表明,该疫苗在pedAIIRD患者中是安全且具有免疫原性的。关于减毒活疫苗接种,有一级证据表明麻疹腮腺炎风疹(MMR)加强疫苗对接受甲氨蝶呤治疗的患者是安全的。此外,有三级证据表明,低剂量糖皮质激素和bDMARDs治疗的患者接种MMR和水痘带状疱疹病毒(VZV)疫苗可能也是安全的。

结论

在过去十年中,关于(减毒活)疫苗在pedAIIRD患者中的安全性和免疫原性的知识显著增加。关于有效性(预防感染)的数据仍然很少。这项SLR的结果是pedAIIRD患者EULAR/PRES更新疫苗接种建议的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f60/9298835/1645a8e368a1/fped-10-910026-g0001.jpg

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