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丙型肝炎病毒相关混合性冷球蛋白血症中冷球蛋白IgM和IgG的体外反应性

In vitro reactivity of cryoglobulin IgM and IgG in hepatitis C virus-associated mixed cryoglobulinemia.

作者信息

Schott P, Polzien F, Müller-Issberner A, Ramadori G, Hartmann H

机构信息

Department of Medicine, Georg-August-University, Göttingen, Germany.

出版信息

J Hepatol. 1998 Jan;28(1):17-26. doi: 10.1016/s0168-8278(98)80197-9.

Abstract

BACKGROUND/AIMS: Mixed cryoglobulinemia is frequently associated with chronic hepatitis C virus infection. We aimed to clarify the mechanism, kinetics and participating proteins in cryoprecipitate formation, which are still being debated.

METHODS

Eighteen patients with cryoglobulinemia were studied. Isolated serum cryoprecipitates and purified cryoglobulin IgM and IgG fractions were analyzed in vitro by turbidimetry for temperature-dependent complex formation. Immunoglobulin reactivity, i.e. in cryoprecipitates and in cryoglobulin-free sera, was studied using immunoblot and enzyme immunoassays. HCV RNA was detected by reverse transcriptase/polymerase chain reaction.

RESULTS

By turbidimetry, purified cryo-IgM precipitated (in the absence of HCV RNA) with cryo-IgG as well as with non-cryoglobulin IgG and with IgG Fc or F(ab')2 fragments. In contrast, purified cryo-IgG did not precipitate with non-cryoglobulin IgM. Anti-HCV IgG reactivity was found in cryoglobulin-free sera, in cryoprecipitates and in purified cryoglobulin IgG fractions. The respective titers were similar. Purified cryo-IgM did not react to HCV-encoded proteins. Binding of cryo-IgM to heterologous IgG was inhibited by intact IgG (up to a mean of about 52%) as well as by IgG Fc (33%) and F(ab')2 fragments (17%). Binding of cryo-IgM to IgG was enhanced at low temperature (4 degrees C vs. 37 degrees C), particularly for type III cryoglobulin IgM.

CONCLUSIONS

In hepatitis C virus-associated cryoglobulinemia the in vitro precipitate formation depended on cryo-IgM, while IgG appeared to act as an unspecific antigenic partner. Hepatitis C viral particles were probably not required. Cryo-IgM binding occurred primarily to intact IgG. Anti-HCV reactivity of either cryo-IgM or cryo-IgG was not necessary for precipitate formation. Regarding the pathogenesis, a direct hepatitis C virus protein-dependent stimulation of B-cells producing cryo-IgM seems to be unlikely.

摘要

背景/目的:混合性冷球蛋白血症常与慢性丙型肝炎病毒感染相关。我们旨在阐明冷沉淀物形成的机制、动力学及相关蛋白,这些问题仍存在争议。

方法

对18例冷球蛋白血症患者进行研究。通过比浊法在体外分析分离出的血清冷沉淀物以及纯化的冷球蛋白IgM和IgG组分,以检测温度依赖性复合物的形成。使用免疫印迹法和酶免疫测定法研究免疫球蛋白反应性,即冷沉淀物中和无冷球蛋白血清中的反应性。通过逆转录/聚合酶链反应检测HCV RNA。

结果

通过比浊法,纯化的冷球蛋白IgM(在无HCV RNA的情况下)可与冷球蛋白IgG、非冷球蛋白IgG以及IgG Fc或F(ab')2片段沉淀。相比之下,纯化的冷球蛋白IgG不会与非冷球蛋白IgM沉淀。在无冷球蛋白血清、冷沉淀物及纯化的冷球蛋白IgG组分中均发现了抗HCV IgG反应性。各自的滴度相似。纯化的冷球蛋白IgM对HCV编码蛋白无反应。完整的IgG(平均高达约52%)以及IgG Fc(33%)和F(ab')2片段(17%)可抑制冷球蛋白IgM与异源IgG的结合。低温(4℃与37℃相比)时冷球蛋白IgM与IgG的结合增强,尤其是III型冷球蛋白IgM。

结论

在丙型肝炎病毒相关的冷球蛋白血症中,体外沉淀物的形成取决于冷球蛋白IgM,而IgG似乎作为非特异性抗原伴侣起作用。可能不需要丙型肝炎病毒颗粒。冷球蛋白IgM主要与完整的IgG结合。冷球蛋白IgM或冷球蛋白IgG的抗HCV反应性对于沉淀物形成并非必需。关于发病机制,丙型肝炎病毒蛋白直接刺激产生冷球蛋白IgM的B细胞似乎不太可能。

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