Kuzichkin D S, Nichiporuk I A, Zhuravleva O A, Markin A A, Rykova M P, Zhuravleva T V, Sadova A A, Kutko O V, Shmarov V A, Ponomarev S A
State Scientific Center of the Russian Federation - Institute for Biomedical Problems of the Russian Academy of Sciences, Moscow, Russia.
NPJ Microgravity. 2022 Nov 2;8(1):46. doi: 10.1038/s41526-022-00237-0.
Space flight factors are known to cause a malfunction in the human immune system and lead to damage to blood vessels. The hemostatic function of endothelium during space missions and its interaction with human immunity has not been determined so far. In this work, we investigated the markers of endothelial activation and damage (plasma concentrations of soluble thrombomodulin fraction (sTM), von Willebrand factor (vWF), highly sensitive C-reactive protein (hs-CRP)), as well as the level of D-dimer and compared them to the immunological parameters characterizing the state of human humoral and cellular immunity. The immune status of long-duration ISS crewmembers was assessed by whole-blood testing, and comprehensive postflight immune assessment included the analysis of leukocyte distribution. Flow cytometry was applied to determine the absolute counts and the percentage of lymphocyte subsets: B cells (CD19), T cells (CD3, CD3CD4, CD3CD8), NK cells (CD3CD16CD56, CD11bCD56), and activated subsets (CD3CD25 and CD3HLA-DR). The in vitro basal cytokine production was investigated in whole blood cell culture. The cytokines IFN-gamma, IL-1-beta, IL-4, IL-6, IL-10, IL-18, and TNF-alpha were measured in plasma and the 24-h supernatants by a sensitive enzyme-linked immunosorbent assay. A significant increase in the plasma levels of vWF and hs-CRP and a decrease in the concentration of sTM after spaceflights were detected. Divergent changes in the parameters characterizing the state of the immune system were observed. We propose that the changes revealed may lead to an increase in the procoagulant activity of blood plasma, suppression of protein C activation and thrombin inhibition, as well as to an increase in the adhesive-aggregate potential of platelets, especially in case of changes in the rheological characteristics of blood flow during re-adaptation to ground conditions. We also speculate that the immune system might play an important role in vessel damage during long-duration missions.
已知太空飞行因素会导致人体免疫系统功能失调并致使血管受损。迄今为止,太空任务期间内皮细胞的止血功能及其与人体免疫的相互作用尚未明确。在本研究中,我们调查了内皮细胞激活和损伤的标志物(可溶性血栓调节蛋白片段(sTM)、血管性血友病因子(vWF)、高敏C反应蛋白(hs-CRP)的血浆浓度)以及D-二聚体水平,并将它们与表征人体体液免疫和细胞免疫状态的免疫学参数进行比较。通过全血检测评估长期国际空间站乘员的免疫状态,飞行后综合免疫评估包括白细胞分布分析。应用流式细胞术确定淋巴细胞亚群的绝对计数和百分比:B细胞(CD19)、T细胞(CD3、CD3CD4、CD3CD8)、自然杀伤细胞(CD3CD16CD56、CD11bCD56)以及活化亚群(CD3CD25和CD3HLA-DR)。在全血细胞培养中研究体外基础细胞因子产生情况。通过灵敏的酶联免疫吸附测定法测量血浆和24小时上清液中的细胞因子干扰素-γ、白细胞介素-1-β、白细胞介素-4、白细胞介素-6、白细胞介素-10、白细胞介素-18和肿瘤坏死因子-α。检测到太空飞行后血浆中vWF和hs-CRP水平显著升高以及sTM浓度降低。观察到表征免疫系统状态的参数出现不同变化。我们认为,所揭示的这些变化可能导致血浆促凝活性增加、蛋白C活化和凝血酶抑制受到抑制,以及血小板黏附聚集潜能增加,尤其是在重新适应地面条件期间血流流变学特性发生变化的情况下。我们还推测,免疫系统可能在长期任务期间的血管损伤中发挥重要作用。