Rauterberg A D, Jung E G, Burger R, Rauterberg E W
Department of Dermatology, Mannheim, University of Heidelberg, F.R.G.
J Invest Dermatol. 1990 Jan;94(1):144-9. doi: 10.1111/1523-1747.ep12873996.
The effect of PUVA treatment on normal human serum (NHS), on isolated PMN, or on C3-deficient guinea pigs and congenic (C3-competent) control animals was tested. At a concentration of 0.1 or 1 mM/l 8-MOP and UVA doses of 5-30 J/cm2, PUVA failed to induce any detectable C3-cleavage in NHS. Furthermore, when the complement (C) activation in NHS had been induced before or after PUVA treatment by various methods. PUVA did not modulate the extent of C3-cleavage. PUVA did not affect the viability of isolated PMN, nor did it induce a release of LDH or elastase. No differences between C3-deficient and C-competent guinea pig skin exposed to PUVA were observed in erythema or histologic responses. Immunohistologic examination of specimens from normal guinea pigs revealed C3b and C3d deposits on necrotic keratinocytes, findings restricted to the PUVA-treated areas. Necrosis of keratinocytes was present in skin specimens of C3-deficient animals from PUVA-treated sites to a similar extent. However, deposits of C3-related antigens were completely absent there. From these observations, we suggest that the induction of phototoxic erythema following PUVA treatment is independent of complement.
测试了补骨脂素加长波紫外线(PUVA)疗法对正常人血清(NHS)、分离的中性粒细胞、C3缺陷豚鼠和同基因(C3正常)对照动物的影响。在8-甲氧基补骨脂素(8-MOP)浓度为0.1或1 mM/l以及UVA剂量为5-30 J/cm2的情况下,PUVA未能在NHS中诱导出任何可检测到的C3裂解。此外,当通过各种方法在PUVA治疗之前或之后诱导NHS中的补体(C)激活时,PUVA并未调节C3裂解的程度。PUVA不影响分离的中性粒细胞的活力,也不诱导乳酸脱氢酶(LDH)或弹性蛋白酶的释放。在红斑或组织学反应方面,未观察到暴露于PUVA的C3缺陷和C正常豚鼠皮肤之间存在差异。对正常豚鼠标本的免疫组织学检查显示,坏死角质形成细胞上有C3b和C3d沉积,这些发现仅限于PUVA治疗区域。PUVA治疗部位的C3缺陷动物皮肤标本中存在角质形成细胞坏死,程度相似。然而,那里完全没有C3相关抗原的沉积。根据这些观察结果,我们认为PUVA治疗后光毒性红斑的诱导与补体无关。