Kawana S, Janson M, Jordon R E
J Invest Dermatol. 1984 May;82(5):506-10. doi: 10.1111/1523-1747.ep12261058.
Although complement is often detected in the intercellular substance of pemphigus skin lesions, the ability of pemphigus antibodies to fix complement in vitro is controversial. The purpose of this study was to test in vitro complement fixation abilities of pemphigus antibodies further using organ and tissue culture methods. Epidermal cell monolayers from mouse tail were incubated with the purified IgG fraction of pemphigus serum followed by purified Clq. Binding of Clq, as well as IgG was demonstrated by immunofluorescence methods. When purified Clq was replaced with normal human serum as a complement source, positive C3 and C4 staining were also evident. When purified IgG of normal human serum was used in place of pemphigus IgG, similar immunofluorescence staining was not observed. Further evidence for complement fixation in vitro by pemphigus antibodies was obtained using organ cultures. Organ culture of normal human skin and monkey esophageal mucosa cultured in purified pemphigus IgG showed intercellular substance binding of IgG. No binding was observed when normal IgG was substituted for pemphigus IgG. Additional organ culture sections were then treated with complement (fresh normal human serum) and tested by in vitro complement staining. Fixation of Clq, C4, and C3 was noted in intercellular substance areas of organ cultured skin and mucosa incubated with pemphigus IgG but not those incubated with normal IgG. Prior treatment of pemphigus IgG organ cultured skin sections with unlabeled anti-C3, blocked positive C3 staining. These results suggest that some pemphigus antibodies are capable of activating complement in vitro.
虽然在天疱疮皮肤损害的细胞间质中常可检测到补体,但天疱疮抗体在体外固定补体的能力仍存在争议。本研究的目的是采用器官和组织培养方法进一步检测天疱疮抗体的体外补体固定能力。将小鼠尾部的表皮细胞单层与天疱疮血清的纯化IgG组分孵育,随后加入纯化的Clq。通过免疫荧光法证实了Clq以及IgG的结合。当用正常人血清替代纯化的Clq作为补体来源时,C3和C4染色阳性也很明显。当用正常人血清的纯化IgG替代天疱疮IgG时,未观察到类似的免疫荧光染色。使用器官培养获得了天疱疮抗体在体外固定补体的进一步证据。在纯化的天疱疮IgG中培养的正常人皮肤和猴食管黏膜的器官培养显示IgG在细胞间质结合。当用正常IgG替代天疱疮IgG时未观察到结合。然后对额外的器官培养切片用补体(新鲜正常人血清)处理并通过体外补体染色进行检测。在与天疱疮IgG孵育的器官培养皮肤和黏膜的细胞间质区域观察到Clq、C4和C3的固定,但与正常IgG孵育的区域未观察到。用未标记的抗C3预先处理天疱疮IgG器官培养的皮肤切片,可阻断C3染色阳性。这些结果表明一些天疱疮抗体能够在体外激活补体。