Khavinson V Kh, Linkova N S, Kvetnoy I M, Polyakova V O, Drobintseva A O, Kvetnaia T V, Ivko O M
Department of Biogerontology, St. Petersburg Institute of Bioregulation and Gerontology, St. Petersburg, Russia.
Group of Peptide Regulation and Aging, I. P. Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg, Russia.
Bull Exp Biol Med. 2020 Nov;170(1):118-122. doi: 10.1007/s10517-020-05016-z. Epub 2020 Nov 25.
Thymalin is a polypeptide complex isolated from the thymus and regulating the functions of the immune system. Thymalin is effective in therapy of acute respiratory syndrome, chronic obstructive bronchitis, and other immunopathology. Thymalin increases functional activity of T lymphocytes, but the targeted molecular mechanism of its biological activity requires further study. We studied the influence of thymalin on differentiation of human hematopoietic stem cells (HSC) and expression of CD28 molecule involved in the implementation of antiviral immunity in COVID-19 infection. It was found that thymalin reduced the expression of CD44 (stem cell marker) and CD117 (molecule of the intermediate stage of HSC differentiation) by 2-3 times and increased the expression of CD28 (marker of mature T lymphocytes) by 6.8 times. This indirectly indicates that thymalin stimulated differentiation of CD117 cells into mature CD28T lymphocytes. It is known that in patients with severe COVID-19, the number of CD28, CD4, CD8T lymphocytes in the blood decreased, which attested to a pronounced suppression of immunity. It is possible that the antiviral effect of thymalin consists in compensatory stimulation of HSC differentiation into CD28T lymphocytes at the stage of immunity suppression in unfavorable course of viral infection. Thymalin can be considered as an immunoprotective peptide drug for the prevention of COVID-19.
胸腺素是一种从胸腺中分离出来的多肽复合物,可调节免疫系统的功能。胸腺素对急性呼吸综合征、慢性阻塞性支气管炎和其他免疫病理学疾病的治疗有效。胸腺素可增加T淋巴细胞的功能活性,但其生物活性的靶向分子机制仍需进一步研究。我们研究了胸腺素对人类造血干细胞(HSC)分化以及参与COVID-19感染中抗病毒免疫实施的CD28分子表达的影响。结果发现,胸腺素可使CD44(干细胞标志物)和CD117(HSC分化中期分子)的表达降低2至3倍,并使CD28(成熟T淋巴细胞标志物)的表达增加6.8倍。这间接表明胸腺素刺激了CD117细胞向成熟CD28 T淋巴细胞的分化。众所周知,在重症COVID-19患者中,血液中CD28、CD4、CD8 T淋巴细胞的数量减少,这证明免疫力受到明显抑制。胸腺素的抗病毒作用可能在于在病毒感染不利过程中的免疫抑制阶段,对HSC分化为CD28 T淋巴细胞进行代偿性刺激。胸腺素可被视为预防COVID-19的免疫保护肽药物。