Approaches to correction of immune system disturbances in post-COVID patients

Maria A. Dobrynina, A. V. Zurochka, V. A. Zurochka, L. V. Ryabova, A. P. Sarapultsev
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Abstract

SARS-CoV-2 virus can induce immune system disorders in post-COVID patients, which may persist for an extended period beyond the acute phase of the disease. Therefore, the search for immunocorrection approaches to address the detected disorders is a significant challenge in clinical immunology. This study aimed to investigate the impact of a synthetic peptide derived from the active center of GM-CSF on the immune system of patients with post-COVID immunopathological syndrome. A total of 21 patients who previously suffered with SARS-CoV-2 infection were included in the study. Flow cytometry was used to analyze various immune cell populations, including panleukocyte markers for gated lymphocytes (CD45+ and CD46+), T lymphocytes (CD3+), helper inducers (CD3+, CD4+), cytotoxic T lymphocytes (CD3+, CD8+), TNK cells (CD3+, CD56+), natural killer cells (CD3-, CD56+), B lymphocytes (CD3-, CD19+), activated helper cells (CD3+, CD4+, CD25+), and activated T lymphocytes (CD3+, HLA-DR). Moreover, IgA, IgM, IgG antibodies specific to SARS-CoV-2, phagocytosis and NBT activity of neutrophils, and complement fragments C1q, C3a, and C5a were assessed. The results demonstrated that topical application of the synthetic peptide derived from the active center of GM-CSF (Acegram-spray) upon mucous membranes significantly influenced the functional bactericidal activity of neutrophils (NBT-activity), increased the percentage of T helper cells, and elevated the C3a complement fragment. These findings indicate that the synthetic peptide primarily affects innate immunity factors. However, no significant differences were observed in other immune system parameters. Therefore, the development of therapeutic approaches for post-COVID patients with impaired immune systems may require a search for additional immunomodulators that target T, B, and NK cells. Further research is needed to explore the effects of various immunomodulators on the immune system of post-COVID patients.
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新冠肺炎后患者免疫系统紊乱的纠正方法
SARS-CoV-2病毒可在covid后患者中诱发免疫系统紊乱,这种紊乱可能在疾病急性期之后持续较长时间。因此,寻找免疫矫正方法来解决检测到的疾病是临床免疫学的一个重大挑战。本研究旨在探讨GM-CSF活性中心衍生的合成肽对covid - 19后免疫病理综合征患者免疫系统的影响。共有21名先前患有SARS-CoV-2感染的患者被纳入该研究。用流式细胞术分析各种免疫细胞群,包括门控淋巴细胞(CD45+和CD46+)、T淋巴细胞(CD3+)、辅助诱导剂(CD3+、CD4+)、细胞毒性T淋巴细胞(CD3+、CD8+)、TNK细胞(CD3+、CD56+)、自然杀伤细胞(CD3-、CD56+)、B淋巴细胞(CD3-、CD19+)、活化辅助细胞(CD3+、CD4+、CD25+)和活化T淋巴细胞(CD3+、HLA-DR)的泛白细胞标记物。此外,还评估了SARS-CoV-2特异性IgA、IgM、IgG抗体、中性粒细胞的吞噬和NBT活性以及补体片段C1q、C3a和C5a。结果表明,GM-CSF活性中心衍生的合成肽(Acegram-spray)局部应用于粘膜可显著影响中性粒细胞的功能性杀菌活性(nbt活性),增加T辅助细胞的百分比,并升高C3a补体片段。这些发现表明,合成肽主要影响先天免疫因子。然而,在其他免疫系统参数中没有观察到显著差异。因此,开发针对免疫系统受损的covid后患者的治疗方法可能需要寻找针对T、B和NK细胞的额外免疫调节剂。各种免疫调节剂对新冠肺炎后患者免疫系统的影响有待进一步研究。
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