COVID-19后急性冠状动脉综合征患者T细胞免疫特征与自然杀伤细胞含量的关系

E. Safronova, L. V. Ryabova
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引用次数: 0

摘要

我们检查了65名患有不稳定心绞痛和急性心肌梗死(急性冠状动脉综合征- ACS)的男性,年龄在40至65岁之间,之前患有COVID-19, 20名患有ACS但未经历COVID-19。所有患者均患有高血压,并在入院后3天内需要行冠状动脉支架置入。从Navios细胞荧光仪(BeckmanCoulter, USA)流式细胞术的免疫学参数来看,根据评估免疫淋巴细胞环节的标准化技术[1],确定如下:)、CD45+CD3+ CD8+(细胞毒性t淋巴细胞)、CD45+CD3+ cd19 + (b淋巴细胞)、CD45+CD3+CD16+CD56+ (TNK细胞)、CD45+CD3-CD16+CD56+(自然杀伤细胞)、CD45+CD3+ CD4+CD25+CD127- (t调节细胞)、CD45+CD3+ CD4+CD25+ CD25+ (t淋巴细胞-早期活化)、CD45+CD3+ CD4+CD25+ (t淋巴细胞-晚期活化)。所有患者根据NK细胞(自然杀伤细胞)的含量进行分组。感染COVID-19的患者有3种表型(NK细胞计数减少、正常和增加),而非幸存者有2种表型(NK细胞计数减少和正常)。感染COVID-19的患者病情最严重,免疫功能紊乱程度最高。在急性冠状动脉综合征合并COVID-19的患者中,NK细胞水平以正常和升高为主,与未合并COVID-19的ACS患者相比,病程更为严重——以急性心肌梗死患者为主,死亡率更高,治疗时间更长,支架内血栓形成也更为常见。在ACS和COVID-19合并NK细胞升高的患者中,t细胞免疫功能的下降幅度最大:一般t淋巴细胞、辅助t淋巴细胞、毒性t淋巴细胞、早期活化t淋巴细胞、调节性t淋巴细胞的绝对数量与其他组相比。在感染COVID-19且NK细胞减少的人群中,免疫调节指数最低,同时t -NK淋巴细胞数量最多。无COVID-19的低NK细胞患者记录了T-NK淋巴细胞的最低数量。在NK细胞升高和正常的COVID-19康复患者中发现了最小的晚期激活t淋巴细胞(CD45+CD3+CD4+HLA-DR+)。未感染COVID-19但接种疫苗且NK细胞含量正常的患者中,晚期活化调节性T细胞数量最少。该研究还使我们能够更清楚地定义需要额外免疫矫正的ACS患者群体。
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Features of T cell immunity depending on the content of natural killer cells in patients with acute coronary syndrome following COVID-19
We examined 65 men with unstable angina and acute myocardial infarction (acute coronary syndrome - ACS) from 40 to 65 years old who had previously had COVID-19 and 20 people with ACS who had not undergone COVID-19. All persons also had hypertension, and they required stenting of the coronary arteries within the next 3 days after admission to the hospital. From the immunological parameters by flow cytometry on the Navios cytofluorimeter (BeckmanCoulter, USA), according to the standardized technology for assessing the lymphocytic link of immunity [1], the following were determined: ), CD45+ CD3+ CD8+ (cytotoxic T-lymphocytes), CD45+CD3-CD19+ (B-lymphocytes), CD45+CD3+CD16+CD56+ (TNK cells), CD45+CD3-CD16+CD56+ (natural killer cells), CD45+ CD3+CD4+CD25+CD127- (T-regulatory cells), CD45+ CD3+CD4+CD25+ (T-lymphocytes - early activation), CD45+CD3+HLA-DR (T-lymphocytes - late activation). All patients were divided into groups depending on the content of NK cells (natural killer cells). Patients who have had COVID-19 have 3 phenotypes of disorders (decreased NK cell count, normal and increased), while non-survivors have 2 phenotypes (decreased NK cell count and normal). The most severe condition and severity of immune disorders were found in patients who had undergone COVID-19. In patients with acute coronary syndrome and COVID-19, predominantly with normal and elevated levels of NK cells, compared with ACS patients without COVID-19, a more severe course of the disease was observed - patients with acute myocardial infarction prevailed, they had a higher mortality rate, the duration of treatment was increased, and stent thrombosis was also more common. In persons with ACS and COVID-19 with elevated NK cells, the maximum decrease in the T-cell immunity was observed: T-lymphocytes of general, T-lymphocytes-helpers, T-cytotoxic lymphocytes, T-lymphocytes of early activation, T-regulatory cells in absolute numbers compared to other groups. The lowest immunoregulatory index and, at the same time, the maximum number of T-NK-lymphocytes were observed in persons who had undergone COVID-19 and had reduced NK cells. The minimum number of T-NK lymphocytes was recorded in patients with low NK cells who did not have COVID-19. Minimal T-lymphocytes (CD45+CD3+CD4+HLA-DR+) of late activation were found in people who recovered from COVID-19 with elevated and normal NK cells. The lowest number of late activation regulatory T cells was observed in patients who did not have COVID-19, but were vaccinated, and had a normal content of NK cells. The study also allows us to more clearly define the groups of patients with ACS who need additional immunocorrection.
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