Schrieber L, Penny R
Rheumatol Int. 1984;4(3):95-109. doi: 10.1007/BF00541177.
In systemic immune complex (IC) diseases such as SLE and rheumatoid vasculitis, IC accumulate in a number of tissues, either after deposition from the circulation or from in situ formation. The tissue localisation of IC depends on a delicate balance between the production of IC and the ability of the mononuclear phagocytic system (MPS) to remove them from blood. At times IC are cleared inefficiently, persist in the circulation and subsequently localise in tissues. This review evaluates the role of local tissue factors - anatomical, physiological, physical and immunological - in this process. We report on our studies examining the significance of C3b and IgG Fc receptors in tissues subject to IC deposition. No evidence for such receptors was found with the exception of a C3b receptor in human glomeruli. Our negative findings may be due to methodological difficulties in the identification of in situ receptors. Alternatively, immune receptors may not be present at these extra-glomerular sites and would therefore be unlikely to participate in IC localisation.
在系统性免疫复合物(IC)疾病如系统性红斑狼疮(SLE)和类风湿性血管炎中,IC会在许多组织中积聚,这要么是循环中沉积所致,要么是原位形成的结果。IC在组织中的定位取决于IC产生与单核吞噬细胞系统(MPS)从血液中清除它们的能力之间的微妙平衡。有时IC清除效率低下,持续存在于循环中,随后在组织中定位。本综述评估了局部组织因素——解剖学、生理学、物理学和免疫学因素——在此过程中的作用。我们报告了我们研究C3b和IgG Fc受体在IC沉积组织中的意义的研究。除了人类肾小球中的C3b受体外,未发现此类受体的证据。我们的阴性结果可能是由于鉴定原位受体存在方法学困难。或者,免疫受体可能不存在于这些肾小球外部位,因此不太可能参与IC定位。