Jablonska S, Chorzelski T P, Jarzabek-Chorzelska M, Beutner E H
Int Arch Allergy Appl Immunol. 1975;48(3):324-40.
Biopsies of skin lesions from 50 cases of psoriasis and from 42 cases with other dermatoses were studied by the methods described in the foregoing report, that is by the four-compartment by the methods described in the foregoing report, that is by the four-compartment immunofluorescent (IF) system for detecting stratum corneum autoantibodies and in vivo binding of IgG in psoriatic scales at the site of the stratum corneum antigen. They were also studied histologically. Early and fully developed psoriatic lesions tended to have more widespread deposits of IgG in the stratum corneum than receding lesions. In biopsies with widespread IgG deposits the stratum corneum antigen usually could not be demonstrated because of blocking by in vivo bound IgG. Of the 42 control biopsies of skin lesions from patients with other dermatoses which were examined with this system two gave the IF staining patterns which were seen most commonly in psoriatic lesions. In these two cases strong widespread IgG deposits occurred in compartment 3, and 4 was very similar to compartment 3. One case was diagnosed as lichen planus and one as cornu cutaneum. Comparisons of the IF findings in psoriatic and control lesion biopsies indicate that significantly more of the former have: (1) IgG deposits at the combining sites of stratum corneum antibodies (92 vs. 50%) and (2) no demonstrable stratum corneum antigen because of 'blocking' by in vivo bound IgG, i.e. compartment 3 like 4 (56 vs. 7%). A highly significant inverse relation between the in vivo deposits of IgG and demonstrability of stratum corneum antigen appeared regardless of the clinical condition. This observation lends support to the view that the IgG which is bound to the sites of the stratum corneum antigen in ski; lesions may in fact be in vivo bound stratum corneum antoantibody.
采用上述报告中描述的方法,即通过四室免疫荧光(IF)系统检测角质层自身抗体以及银屑病鳞屑中IgG在角质层抗原部位的体内结合情况,对50例银屑病患者和42例其他皮肤病患者的皮肤病变活检标本进行了研究。同时也进行了组织学研究。早期和完全发展的银屑病病变在角质层中IgG的沉积往往比消退期病变更为广泛。在IgG广泛沉积的活检标本中,由于体内结合的IgG的阻断作用,通常无法显示角质层抗原。在使用该系统检查的42例其他皮肤病患者的皮肤病变对照活检标本中,有两例呈现出银屑病病变中最常见的IF染色模式。在这两例中,第3室出现了强烈而广泛的IgG沉积,第4室与第3室非常相似。一例被诊断为扁平苔藓,另一例为角质瘤。银屑病病变活检标本和对照病变活检标本的IF结果比较表明,前者中显著更多的标本有:(1)角质层抗体结合部位的IgG沉积(92%对50%)以及(2)由于体内结合的IgG“阻断”而无法显示角质层抗原,即第3室类似第4室(56%对7%)。无论临床情况如何,IgG的体内沉积与角质层抗原的可显示性之间都呈现出高度显著的负相关。这一观察结果支持了这样一种观点:皮肤病变中与角质层抗原部位结合的IgG实际上可能是体内结合的角质层自身抗体。