Clinical and Immunologic Effects of Paraprobiotics in Long-COVID Patients: A Pilot Study.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
María José Docampo, Mattei Batruch, Pietro Oldrati, Ernesto Berenjeno-Correa, Marc Hilty, Gabriel Leventhal, Andreas Lutterotti, Roland Martin, Mireia Sospedra
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引用次数: 0

Abstract

Background and objectives: After the enormous health burden during the acute stages of the COVID-19 pandemic, we are now facing another important challenge, that is, long-COVID, a clinical condition with often disabling signs and symptoms of the neuropsychiatric, gastrointestinal, respiratory, cardiovascular, and immune systems. While the pathogenesis of this syndrome is still poorly understood, alterations of immune function and the gut microbiota seem to play important roles. Because affected individuals are frequently unable to work for prolonged periods and suffer numerous health compromises, effective treatments represent a major unmet medical need. Multiple potential therapies have been tried, but none is approved yet. Approaches that are able to influence the immune system and gut microbiota such as probiotics and paraprobiotics, i.e., nonviable probiotics, seem promising candidates. We, therefore, evaluated the clinical and immunologic effects of paraprobiotics in a small pilot study.

Methods: A total of 6 patients with long-COVID were followed systematically for more than 12 months after disease onset using standardized validated questionnaires, a smartphone app, and wearable sensors to assess neurocognitive function, fatigue, depressiveness, autonomic nervous system alterations, and quality of life. We then offered patients defined paraprobiotics for 4 weeks and evaluated them at the end of the treatment period using the same questionnaires, smartphone app, and wearable sensors. In addition, a comprehensive immunophenotyping and gut microbiota analysis was performed before and after treatment.

Results: Improvements in several of the neurologic symptoms such as dysautonomia, fatigue, and depression were documented using both patient-reported outcomes and data from the smartphone app and wearable sensors. Of interest, the expression of activation markers on some immune cell populations such as B cells and nonclassical monocytes and the expression of toll-like receptor 2 (TLR2) on T cells were reduced after paraprobiotics treatment.

Discussion: Our results suggest that paraprobiotics might exert positive effects in patients with long-COVID most likely by modulating immune cell activation and expression of TLR2 on T cells. Further studies with paraprobiotics should confirm the promising observations of this small pilot study and hopefully not only improve the outcome of long-COVID but also unravel the pathomechanisms of this condition.

Classification of evidence: This study provides Class IV evidence that paraprobiotics increase the probability of favorable changes of clinical and immunologic markers in patients with long-COVID.

副微生物药物对长期慢性乙型肝炎患者的临床和免疫学影响:一项试点研究。
背景和目标:在 COVID-19 大流行的急性期造成了巨大的健康负担之后,我们现在面临着另一个重要的挑战,即长期 COVID,这是一种临床症状和体征通常会导致神经精神、胃肠道、呼吸道、心血管和免疫系统失能的疾病。虽然人们对这种综合征的发病机理还知之甚少,但免疫功能和肠道微生物群的改变似乎起着重要作用。由于患者经常长期无法工作,健康受到严重损害,因此有效的治疗方法是一项尚未得到满足的重大医疗需求。目前已经尝试了多种潜在疗法,但还没有一种获得批准。能够影响免疫系统和肠道微生物群的方法,如益生菌和副益生菌(即不能存活的益生菌)似乎很有希望。因此,我们在一项小型试点研究中评估了副益生菌的临床和免疫学效果:方法:共对 6 名长期慢性阻塞性肺气肿患者进行了为期 12 个多月的系统随访,随访过程中使用了标准化验证问卷、智能手机应用程序和可穿戴传感器,以评估神经认知功能、疲劳、抑郁、自主神经系统改变和生活质量。然后,我们为患者提供了为期 4 周的定义副作用药物,并在治疗期结束时使用相同的问卷、智能手机应用程序和可穿戴传感器对患者进行评估。此外,在治疗前后还进行了全面的免疫分型和肠道微生物群分析:结果:利用患者报告的结果以及智能手机应用程序和可穿戴传感器的数据,记录了一些神经症状的改善情况,如自主神经功能障碍、疲劳和抑郁。值得关注的是,一些免疫细胞群(如 B 细胞和非典型单核细胞)的活化标志物的表达以及 T 细胞的收费样受体 2 (TLR2) 的表达在副生化药物治疗后有所减少:我们的研究结果表明,副微生物制剂可能通过调节免疫细胞的活化和 T 细胞上 TLR2 的表达,对长期 COVID 患者产生积极影响。对副微生物制剂的进一步研究应能证实这项小型试点研究的观察结果,并希望不仅能改善长COVID的治疗效果,还能揭示这种疾病的病理机制:本研究提供了IV级证据,证明副粘菌素可提高长COVID患者临床和免疫学指标发生有利变化的概率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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