Witte T
Klinik für Immunologie und Rheumatologie, Carl-Neuberg-Str. 1, 30625, Hannover, Deutschland.
Radiologe. 2016 Dec;56(12):1043-1048. doi: 10.1007/s00117-016-0188-5.
In contrast to the other IgG subclasses, IgG4 does not bind to low affinity Fc receptors or activate the classical complement pathway. In addition, it is unstable and can dissociate into two hemimolecules; therefore, IgG4 most likely has an immunosuppressive role. On the other hand, there a few examples of an immunostimulatory role of IgG4 antibodies; therefore, the function of IgG4 in IgG4 related diseases is not yet entirely clear. The trigger factors of IgG4 related diseases (allergic or autoimmune) are still under debate. The activation of T helper (Th) 2 and regulatory T cells has been shown to be important in the pathophysiology of IgG4 related diseases as they produce cytokines which contribute to the formation of IgG4 and to fibrosis of various tissues.
与其他IgG亚类不同,IgG4不与低亲和力Fc受体结合,也不激活经典补体途径。此外,它不稳定,可解离成两个半分子;因此,IgG4很可能具有免疫抑制作用。另一方面,也有一些IgG4抗体具有免疫刺激作用的例子;因此,IgG4在IgG4相关疾病中的功能尚未完全明确。IgG4相关疾病(过敏性或自身免疫性)的触发因素仍存在争议。已证明辅助性T(Th)2细胞和调节性T细胞的激活在IgG4相关疾病的病理生理学中很重要,因为它们产生的细胞因子有助于IgG4的形成和各种组织的纤维化。