人甲胎蛋白(AFP)特异性肽序列修复fas介导的心肌炎患者淋巴细胞凋亡(13-19)

Alexander N. Kazimirsky, Alexander A. Terentev, Jean M. Salmasi, Gennady V. Poryadin
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引用次数: 0

摘要

人甲胎蛋白(AFP)能够调节细胞增殖过程。研究了人AFP分子中参与受体相互作用部分的合成肽的调控特性,该肽由7个氨基酸组成,氨基酸序列为LDSYQCT。对6例免疫性心肌炎患者病情加重期的外周血淋巴细胞进行了研究。对于这类患者,早期活化抗原的表达水平明显升高,同时伴有诱导fas介导的细胞凋亡的平行干扰。结果表明,该肽对观察患者CD23、CD25和CD71淋巴细胞早期活化标志物的表达几乎没有影响。由于多肽的作用,免疫性心肌炎患者在病情加重期晚期活化抗原HLA DR的表达由15.36 +/- 1.77%显著降低至9.21 +/- 1.46% (p < 0.05)。相反,fas介导的凋亡受体的表达在疾病加重期降低,在肽AFP(13-19)的作用下,从2.85 +/- 0.57%显著增加到9.09 +/- 1.37% (p < 0.01)。因此,使用合成AFP片段可以在体外恢复疾病情况下淋巴细胞的正常活化凋亡水平,其基础是免疫损伤过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Restoration of FAS-Mediated Apoptosis of Lymphocytes in Patients with Myocarditis by Specific Peptide Sequence of Human Alpha-Fetoprotein (AFP(13-19)).

Human alpha-fetoprotein (AFP) is capable of modulating cellular proliferative processes. A study has been made of the regulatory properties of a synthetic peptide corresponding to the part of the human AFP molecule participating in receptor interaction, the peptide consisting of seven amino acids and having an amino acid sequence LDSYQCT. The study was carried out on the lymphocytes of the peripheral blood of six patients with immune myocarditis in the period of exacerbation of the illness. For such patients a marked increased level of expression of early activation antigens with parallel disturbance of the induction of Fas-mediated apoptosis is typical. It is shown that the peptide had hardly any effect on the expression of early markers of activation of CD23, CD25 and CD71 lymphocytes in the patients being observed. Due to the effect of the peptide, the expression of the late activation antigen HLA DR, greater in patients with immune myocarditis in the period of exacerbation of the illness, is significantly reduced from 15.36 +/- 1.77% to 9.21 +/- 1.46% (p < 0.05). To the contrary, the expression of a receptor of Fas-mediated apoptosis, reduced in the period of exacerbation of the illness, significantly increases under the effect of the peptide AFP(13-19) from 2.85 +/- 0.57% to 9.09 +/- 1.37% (p < 0.01). Thus, the use of the synthetic AFP fragment makes it possible to restore the normal level of the activation apoptosis of lymphocytes in vitro in the case of diseases, at the base of which lie a process of immune damage.

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