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在针对病毒抗原和不匹配的人类白细胞抗原(HLA)抗原的免疫反应过程中,无β2-微球蛋白的HLA I类重链血清水平升高。

Increased beta2-microglobulin-free HLA class I heavy chain serum levels in the course of immune responses to viral antigens and to mismatched HLA antigens.

作者信息

Puppo F, Brenci S, Contini P, Bignardi D, Hamby C V, Filaci G, Ghio M, Scudeletti M, Picciotto A, Indiveri F, Ferrone S

机构信息

Department of Internal Medicine, University of Genoa, Italy.

出版信息

Tissue Antigens. 2000 Apr;55(4):333-41. doi: 10.1034/j.1399-0039.2000.550407.x.

Abstract

Besides being present in serum in association with beta2-mu, HLA class I heavy chains are also present in serum as beta2-micro-free moieties. The increase in serum levels of beta2-micro-associated HLA class I heavy chains in conditions associated with an activation of the immune system have prompted us to measure the serum levels of beta2-mu-free HLA class I heavy chains in the course of immune responses to viral antigens and to mismatched histocompatibility antigens. The serum level of beta2-mu-free HLA class I heavy chains, like that of beta2-mu-associated HLA class I heavy chains was significantly increased in patients affected by advanced HIV-1 infection or by chronic hepatitis C (CHC). In the latter group of patients an association was found between a reduction in the beta2-mu-free HLA class I heavy chain serum level and response to therapy with interferon alpha and ribavirin. Moreover, the beta2-mu-free HLA class I heavy chain serum level was increased more than that of beta2-mu-associated HLA class I heavy chains during episodes of liver ischemia following liver transplantation and in the course of acute graft rejection and of acute graft-versus-host-disease (GVHD) after allogeneic bone marrow transplantation (BMT). These results suggest that the serum levels of beta2-mu-free and beta2-mu-associated HLA class I heavy chains are independently regulated. Furthermore, beta2-mu-free HLA class I heavy chain serum level may be a useful marker to monitor response to therapy in CHC patients and the clinical course of liver and bone marrow grafts.

摘要

除了与β2-微球蛋白结合存在于血清中外,HLA I类重链也以无β2-微球蛋白的部分形式存在于血清中。与免疫系统激活相关疾病中,血清中与β2-微球蛋白结合的HLA I类重链水平升高,促使我们测定在针对病毒抗原和不匹配组织相容性抗原的免疫反应过程中血清中无β2-微球蛋白的HLA I类重链水平。晚期HIV-1感染或慢性丙型肝炎(CHC)患者中,无β2-微球蛋白的HLA I类重链血清水平,与有β2-微球蛋白结合的HLA I类重链血清水平一样,显著升高。在后一组患者中,发现无β2-微球蛋白的HLA I类重链血清水平降低与干扰素α和利巴韦林治疗反应之间存在关联。此外,在肝移植后的肝缺血发作期间以及同种异体骨髓移植(BMT)后的急性移植物排斥和急性移植物抗宿主病(GVHD)过程中,无β2-微球蛋白的HLA I类重链血清水平的升高幅度大于有β2-微球蛋白结合的HLA I类重链血清水平。这些结果表明,无β2-微球蛋白和有β2-微球蛋白结合的HLA I类重链血清水平是独立调节的。此外,无β2-微球蛋白的HLA I类重链血清水平可能是监测CHC患者治疗反应以及肝脏和骨髓移植物临床病程的有用标志物。

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