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可溶性细胞因子受体:基础免疫学与临床应用

Soluble cytokine receptors: basic immunology and clinical applications.

作者信息

Fernandez-Botran R

机构信息

Department of Pathology & Laboratory Medicine, School of Medicine, University of Louisville, KY 40292, USA.

出版信息

Crit Rev Clin Lab Sci. 1999 Jun;36(3):165-224. doi: 10.1080/10408369991239196.

Abstract

Cytokine activity is tightly regulated at multiple levels. Soluble cytokine receptors (sCR) contribute to the regulation of cytokine activity by modulating the ability of cytokines to bind their membrane receptors and generating a response. Endogenous sCR are generated by proteolytic cleavage or "shedding" of the membrane receptor and/or by translation from alternatively spliced messages different from those encoding the membrane forms. The resulting soluble receptors retain their ligand-binding ability and with some exceptions act as competitive inhibitors of the binding and biologic activity of their ligand, both in vitro and in vivo. However, sCR can also have certain effects on cytokines, such as structural stabilization, protection from proteolysis, and prolonged in vivo half-life, which are consistent with an added role as carrier proteins, and which may under some conditions result in potentiation of cytokine activity in vivo. The exact contribution of endogenous sCR to the regulation of immune or inflammatory responses has not yet been established unequivocally. Nonetheless, evidence indicates that the levels of certain sCR in serum and biological fluids correlate with immunological activation and/or disease activity in a variety of clinical conditions. Hence, sCR levels may have significant value as markers in disease management and prognosis. Moreover, sCR have also shown promising potential as immunotherapeutic agents for a variety of clinical disorders, including sepsis, inflammation, and autoimmune and malignant diseases.

摘要

细胞因子活性在多个水平上受到严格调控。可溶性细胞因子受体(sCR)通过调节细胞因子与其膜受体结合并产生反应的能力,来参与细胞因子活性的调控。内源性sCR由膜受体的蛋白水解切割或“脱落”,和/或由与编码膜形式的信息不同的选择性剪接信息翻译产生。所产生的可溶性受体保留其配体结合能力,并且除了某些例外情况,在体外和体内均作为其配体结合和生物活性的竞争性抑制剂起作用。然而,sCR也可对细胞因子产生某些影响,如结构稳定、防止蛋白水解以及延长体内半衰期,这些作用与作为载体蛋白的附加作用一致,并且在某些情况下可能导致体内细胞因子活性增强。内源性sCR对免疫或炎症反应调节的确切贡献尚未明确确定。尽管如此,有证据表明,血清和生物体液中某些sCR的水平与多种临床情况下的免疫激活和/或疾病活动相关。因此,sCR水平作为疾病管理和预后的标志物可能具有重要价值。此外,sCR作为多种临床疾病(包括败血症、炎症、自身免疫性疾病和恶性疾病)的免疫治疗药物也显示出有前景的潜力。

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