COVID-19患者免疫介导的风湿病临床生物学和进化参数的特殊性-系统文献综述

A. Trandafir, G. Onose, Constantin Munteanu, M. Băilă, A. Saglam, M. Mandu, I. Saulescu, Elena Grădinaru, V. Bojinca
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引用次数: 0

摘要

背景:自2019年爆发以来,冠状病毒病2019 (COVID-19)/严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)已成为严重的医疗威胁,并被宣布为全球大流行,引发了全球人民的恐惧、恐慌和不确定性。在这些人中,有一类特殊的患者——那些患有免疫介导的风湿病(IMIDs)的患者——他们的诊断是不惜一切代价避免感染,因为这会对免疫系统和整体反应性产生额外的负面影响。综上所述,我们的目的是深入了解在SARS-CoV-2 (SARS-CoV-2)背景下IMIDs患者的免疫系统与疾病的真正负担和COVID-19疫苗接种之间的关系。材料和方法:在这方面,我们根据“首选红色报告项目用于系统评价和meta分析(PRISMA)”的概念进行了彻底的系统文献综述。按照五步算法,我们首先选择了745篇发表在知名国际医学数据库(isi索引)中的文章,时间为2021年1月1日至2022年12月31日。在排除重复、非英语写作和“开放获取”的文章后,然后应用PEDro分类/评分启发,只有58篇文章被选中进行深入的全面定性阅读。在最后一个阶段,有20篇文章因为没有提供重要的信息而被“排除在外”。因此,在我们的系统文献综述中,纳入了38篇文章。结果:在本综述收集的数据中,我们描述了COVID-19引发免疫系统激活的分子途径,对感染新型冠状病毒的IMID患者的临床和临床旁意义重大。如果诊断为SARS-CoV2, IMIDs患者住院的风险更高,更容易出现严重后果和死亡。与严重后果和死亡相关的危险因素有:年龄、合并症、潜在疾病活动性、使用的治疗方法(“好的”是抗肿瘤坏死因子α,“坏的”是甲氨蝶呤、磺胺嘧啶、硫唑嘌呤,“坏的”是抗CD20单克隆抗体)。在2019冠状病毒病后和接种该疾病疫苗后,有几起暴发和新发IMIDs的报告,但来自大型研究和登记的数据并未证实暴发或新发IMIDs的发生率更高。关于疫苗接种,越来越重要的是免疫调节剂和免疫抑制剂与疫苗施用之间的时间安排。最后但并非最不重要的是,我们讨论了Long COVID以及人工智能在大流行和相关药物开发中的作用。讨论与结论:我们系统文献综述的数据与我们临床实践的专业知识一致。本文是博士研究的第一部分,集中在相同的主题上,当前的目标是深化关于COVID-19/SARS-CoV2和免疫介导的风湿性疾病交叉的知识,未来的目标是:将我们在这里合成的信息与我们的数据库中近170名患有IMID和COVID-19/SARS-CoV2的罗马尼亚患者进行比较。下一个目标是将研究扩展到多中心对照研究。关键词:SARS-CoV2, COVID-19,免疫介导的风湿病,类风湿关节炎,系统性红斑狼疮,COVID-19疫苗,长COVID
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Particularities regarding Clinical-biological and Evolutive Parameters of Immune-mediated Rheumatic Diseases in Patients with COVID-19 – systematic literature review
Background: Since its outbreak in 2019, Coronavirus disease 2019 (COVID-19)/Severe Acu-te Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) was a serious medical threat and was declared Global Pandemic, triggering fear, panic and uncertainty for people around the Globe. Among those individuals, there is a specific category of patients – the ones with immune-mediated rheumatic diseases (IMIDs) – whose mantra from the diagnosis was to avoid infections at all costs because of the additional negative impact on the immune sys-tem and overall reactivity. Objective: Considering the aforementioned, our objective is to understand the in-depth relation of the immune system of patients with IMIDs in the set-ting of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), and the real bur-den of the disease and vaccination against COVID-19. Materials and Methods: In this res-pect, we have conducted a thoroughly systematic literature review according to the “Prefer-red Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)” concept. Following its five-steps algorithm, we first selected 745 articles that were published in re-putable international medical databases, ISI-indexed, for the period 1 January, 2021–31 December, 2022. After consequent elimination of duplicates, of articles that were not En-glish-written and “open access” and then applying PEDro classification/scoring-inspired, only 58 articles were selected for in-depth full qualitative reading. In the last stage,20 arti-cles were “excluded with reasons”, because they didn’t offer significant information. The-refore, in our systematic literature review, 38 articles were included.Results: In the data gathered in this review we described the molecular pathways of activation of the immune system triggered by COVID-19, with significance on the clinical and paraclinical aspects of IMID patients infected with the new Coronavirus. Patients with IMIDs are at higher risk for hospitalization if diagnosed with SARS-CoV2 and more prone to severe outcomes and death. Risk factors associated with severe outcomes and death are: age, comorbidities, un-derlying disease activity, therapies used (“the good” being anti-tumor necrosis factor α, “the bad” – Methotrexate, Sulfasalazine, Azathioprine and “the ugly” – anti CD20 mono-clonal antibodies). There were several reports of flares and new-onset of IMIDs after CO-VID-19 and after vaccination against this disease, but data from larger studies and registri-es do not confirm higher incidence of flare-ups or new-onset IMIDs. Regarding vaccination, of mounting importance is the timing between immunomodulatory and immunosuppres-sive agents and the administration of the vaccine. And last but not the least, we discussed about Long COVID and the role of artificial intelligence in the pandemic and related-drug development. Discussion and Conclusion: The data in our systematic literature review is consistent with the expertise from our clinical practice. This article is the first part of the doctoral study that is centralized on the same topics, with the current objective of deepe-ning the knowledge about the intersection of COVID-19/SARS-CoV2 and immune-mediated rheumatic diseases and a future objective: to compare information we have synthetized here with our database of almost 170 Romanian patients with a IMID and COVID-19/SARS-CoV2. The next objective is to extend the study to a multicenter control one. Keywords: SARS-CoV2, COVID-19, Immune Mediated Rheumatic Diseases, Rheumatoid Arthri-tis, Systemic Lupus Erythematosus, COVID-19 Vaccine, Long COVID
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