冠心病合并稳定型心绞痛与急性冠脉综合征患者免疫系统状态的比较

O. Lomakovsky, T. Gavrilenko, O. Parkhomenko, M. Lutay, O. A. Pidgaina, N. Rizhkova
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To determine the parameters of cellular and humoral innate and adaptive immunity in blood serum and supernatants of mononuclear cells, enzyme immunoassay was used.Results and discussion. In patients with coronary artery disease with acute coronary syndrome with ST segment elevation compared with patients with coronary artery disease with stable angina pectoris, the levels of indicators of the immune status in the blood were: CRP – 9.3 (5.3–12.0) versus 4.8 (2.4–8.1) mg/L (p=0.0001), sICAM – 785 (690–830) versus 565 (406–744) ng/ml (p=0.0001), IL-10 in blood mononuclear cells – 48 (1–228) versus 194 (21–758) pg/ml (p=0.0007), circulating immune complexes – 90 (70–108) versus 76 (54–105) od. (p=0.045), lymphocytes with apoptosis (CD95) – 16 (9–27) versus 11 (8–17) % (p=0.029), spontaneous oxygen-dependent metabolism of monocytes – 16 (12–21) versus 13 (9–17) (p=0.001). The levels of indicators of the immune system in the blood in patients with coronary artery disease with acute coronary syndrome with ST segment elevation compared with patients with coronary artery disease with acute coronary syndrome without ST segment elevation were: T-helpers – 37 (32–41) versus 42 (37–48) % (p=0.0006) (R=–0.33; p=0.0005), reaction of lymphocyte blast transformation to nonspecific antigen – 38 (32–47) versus 50 (42–61) % (p=0.0004) (R=–0.37; p=0.0003).Conclusions. The development of acute coronary syndrome is directly combined with increased activity of the immune system, as evidenced by the high production of proinflammatory CRP, IL-8, sICAM with a low level of anti-inflammatory IL-10, a pronounced humoral adaptive immune response (in terms of antibodies to the myocardium and vascular tissues, CD40, circulating immune complexes) and active functional state of monocytes (according to cNCT test, functional reserve, phagocytosis) in patients with coronary artery disease with acute coronary syndrome, regardless of the position of the ST segment in comparison with patients with stable coronary artery disease. Elevated levels of antibodies to the myocardium in patients with stable coronary heart disease indicate moderate myocardial damage due to temporary ischemia in angina attacks, even with a stable course of the disease. In patients with acute coronary syndrome, high levels of antibodies to the myocardium indicate myocardial damage due to increased ischemia in plaque destabilization much earlier than the clinical manifestations of acute coronary syndrome. In acute coronary syndrome with ST-segment elevation, compared with ACS patients without ST-segment elevation, activation of neutrophils and suppression of the activity of adaptive T-cell immunity is noted (by the level of T-helpers, sCD40L, blast transformation of lymphocytes, γ-interferon in mononuclear cells, apoptosis of lymphocytes).","PeriodicalId":23419,"journal":{"name":"Ukrainian Journal of Cardiology","volume":"21 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative characteristics of the state of the immune system in patients with coronary artery disease with stable angina pectoris and acute coronary syndrome\",\"authors\":\"O. Lomakovsky, T. Gavrilenko, O. Parkhomenko, M. Lutay, O. A. Pidgaina, N. 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引用次数: 0

摘要

目的-评估免疫系统状态与IHD患者急性冠脉综合征发展之间的关系。材料和方法。第一组64例st段抬高急性冠脉综合征患者,平均年龄54(49 ~ 64)岁;第二组223例冠心病伴稳定型外伤性心绞痛患者,FC II-III,平均年龄56(49-63)岁;第三组47例急性冠状动脉综合征,无ST段抬高,平均年龄61(52 ~ 65)岁。免疫学研究的材料是外周静脉血。采用酶免疫分析法测定单核细胞血清和上清液的细胞和体液固有免疫和适应性免疫参数。结果和讨论。冠心病合并急性冠状动脉综合征ST段抬高患者与冠心病合并稳定型心绞痛患者相比,血液中免疫状态指标水平为:CRP - 9.3 (5.3-12.0) vs 4.8 (2.4-8.1) mg/L (p=0.0001), sICAM - 785 (690-830) vs 565 (406-744) ng/ml (p=0.0001),血单核细胞IL-10 - 48 (1-228) vs 194 (21-758) pg/ml (p=0.0007),循环免疫复合物- 90 (70-108)vs 76 (54-105) od。(p=0.045),凋亡淋巴细胞(CD95) - 16(9-27)比11 (8-17)% (p=0.029),单核细胞自发氧依赖代谢- 16(12-21)比13 (9-17)(p=0.001)。冠心病合并急性冠状动脉综合征伴ST段抬高患者与冠心病合并急性冠状动脉综合征伴ST段抬高患者血液中免疫系统各项指标的水平分别为:辅助t - 37(32-41) %与42 (37 - 48)% (p=0.0006) (R= - 0.33;p=0.0005),淋巴细胞转化为非特异性抗原的反应- 38(32-47)比50 (42-61)% (p=0.0004) (R= - 0.37;.Conclusions p = 0.0003)。急性冠状动脉综合征的发生与免疫系统活性的升高直接相关,如促炎CRP、IL-8、sICAM和低水平抗炎IL-10的高水平产生,明显的体液适应性免疫反应(针对心肌和血管组织的抗体、CD40、循环免疫复合物)和单核细胞活跃的功能状态(根据cNCT测试,功能储备,冠状动脉疾病合并急性冠状动脉综合征的患者,无论ST段的位置如何,与稳定型冠状动脉疾病患者相比。稳定型冠心病患者心肌抗体水平升高表明心绞痛发作时暂时性缺血引起的中度心肌损伤,即使病程稳定。在急性冠脉综合征患者中,高水平的心肌抗体提示由于斑块不稳定的缺血增加而引起的心肌损害,比急性冠脉综合征的临床表现要早得多。st段抬高的急性冠脉综合征患者与无st段抬高的ACS患者相比,中性粒细胞的激活和适应性t细胞免疫活性的抑制(通过t辅助细胞、sCD40L、淋巴细胞的原细胞转化、单核细胞γ-干扰素、淋巴细胞凋亡的水平)被注意到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative characteristics of the state of the immune system in patients with coronary artery disease with stable angina pectoris and acute coronary syndrome
The aim – to assess the relationship between the state of the immune system and the development of acute coronary syndrome in patients with IHD.Materials and methods. The first group consisted of 64 patients with ST-segment elevation acute coronary syndrome, mean age 54 (49–64) years; the second group – 223 patients with coronary artery disease with stable exertional angina, FC II–III, mean age 56 (49–63) years; the third group – 47 patients with acute coronary syndrome without ST segment elevation, mean age 61 (52–65) years. The material for the immunological study was peripheral venous blood. To determine the parameters of cellular and humoral innate and adaptive immunity in blood serum and supernatants of mononuclear cells, enzyme immunoassay was used.Results and discussion. In patients with coronary artery disease with acute coronary syndrome with ST segment elevation compared with patients with coronary artery disease with stable angina pectoris, the levels of indicators of the immune status in the blood were: CRP – 9.3 (5.3–12.0) versus 4.8 (2.4–8.1) mg/L (p=0.0001), sICAM – 785 (690–830) versus 565 (406–744) ng/ml (p=0.0001), IL-10 in blood mononuclear cells – 48 (1–228) versus 194 (21–758) pg/ml (p=0.0007), circulating immune complexes – 90 (70–108) versus 76 (54–105) od. (p=0.045), lymphocytes with apoptosis (CD95) – 16 (9–27) versus 11 (8–17) % (p=0.029), spontaneous oxygen-dependent metabolism of monocytes – 16 (12–21) versus 13 (9–17) (p=0.001). The levels of indicators of the immune system in the blood in patients with coronary artery disease with acute coronary syndrome with ST segment elevation compared with patients with coronary artery disease with acute coronary syndrome without ST segment elevation were: T-helpers – 37 (32–41) versus 42 (37–48) % (p=0.0006) (R=–0.33; p=0.0005), reaction of lymphocyte blast transformation to nonspecific antigen – 38 (32–47) versus 50 (42–61) % (p=0.0004) (R=–0.37; p=0.0003).Conclusions. The development of acute coronary syndrome is directly combined with increased activity of the immune system, as evidenced by the high production of proinflammatory CRP, IL-8, sICAM with a low level of anti-inflammatory IL-10, a pronounced humoral adaptive immune response (in terms of antibodies to the myocardium and vascular tissues, CD40, circulating immune complexes) and active functional state of monocytes (according to cNCT test, functional reserve, phagocytosis) in patients with coronary artery disease with acute coronary syndrome, regardless of the position of the ST segment in comparison with patients with stable coronary artery disease. Elevated levels of antibodies to the myocardium in patients with stable coronary heart disease indicate moderate myocardial damage due to temporary ischemia in angina attacks, even with a stable course of the disease. In patients with acute coronary syndrome, high levels of antibodies to the myocardium indicate myocardial damage due to increased ischemia in plaque destabilization much earlier than the clinical manifestations of acute coronary syndrome. In acute coronary syndrome with ST-segment elevation, compared with ACS patients without ST-segment elevation, activation of neutrophils and suppression of the activity of adaptive T-cell immunity is noted (by the level of T-helpers, sCD40L, blast transformation of lymphocytes, γ-interferon in mononuclear cells, apoptosis of lymphocytes).
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