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人血清中天然抗角蛋白抗体的比较研究。

Comparative studies on naturally occurring antikeratin antibodies in human sera.

作者信息

Iwatsuki K, Viac J, Reano A, Morera A, Staquet M J, Thivolet J, Monier J C

出版信息

J Invest Dermatol. 1986 Aug;87(2):179-84. doi: 10.1111/1523-1747.ep12695322.

Abstract

Comparative studies on the specificity of the so-called antiepidermal antibodies (Abs) found in human sera were performed by immunoblotting, enzyme-linked immunosorbent assay (ELISA), and immunoelectron microscopy (IEM). After a screening test by indirect immunofluorescence (IF), sera obtained from patients with various diseases and controls could be classified in 5 different groups according to the IF patterns on the epidermis: sera reactive with: (1) the stratum corneum (SC); (2) the upper layer (U-Cyt); (3) the whole epidermis (G-Cyt); (4) basal cells (B-Cyt); and (5) negative ones. By immunoblotting, all the 23 IF-positive sera were found to bind to one or more keratin bands, and did not show any reactivity with epidermal Nonidet P-40 soluble proteins. SC-Abs were mainly directed against a 67 kD Keratin band, whereas U-Cyt- and G-Cyt-Abs bound to both 58-56 kD and 67-63 kD keratins. B-Cyt-Abs reacted strongly with 63 kD Keratins and slightly with a 50 kD band. Antikeratin Abs were detected by immunoblotting even in the IF-negative sera. The ELISA study showed that sera with high IF titers contained high levels of antikeratin Abs. In the IEM study using sera containing U-Cyt- or B-Cyt-Abs, 2 distinct reaction patterns were demonstrated: U-Cyt-Abs stained tonofilaments of suprabasal keratinocytes, while B-Cyt-Abs characteristically reacted with those of basal cells. Moreover, SC-, U-Cyt-, and G-Cyt-Abs were absorbed out by insoluble epidermal proteins, and B-Cyt-Abs were decreased in titer after the absorption test. The present study provides strong evidence that most, though not all, human antiepidermal Abs are directed against different keratin polypeptides, and that antikeratin Abs commonly occur in almost all human sera.

摘要

通过免疫印迹法、酶联免疫吸附测定(ELISA)和免疫电子显微镜(IEM)对人血清中发现的所谓抗表皮抗体(Abs)的特异性进行了比较研究。通过间接免疫荧光(IF)进行筛选试验后,根据表皮上的IF模式,从患有各种疾病的患者和对照中获得的血清可分为5个不同的组:与以下物质反应的血清:(1)角质层(SC);(2)上层(U-Cyt);(3)整个表皮(G-Cyt);(4)基底细胞(B-Cyt);以及(5)阴性血清。通过免疫印迹法,发现所有23份IF阳性血清均与一条或多条角蛋白条带结合,并且与表皮非离子去污剂P-40可溶性蛋白无任何反应性。SC-Abs主要针对一条67 kD的角蛋白条带,而U-Cyt-和G-Cyt-Abs则与58 - 56 kD和67 - 63 kD的角蛋白结合。B-Cyt-Abs与63 kD角蛋白强烈反应,与一条50 kD条带轻微反应。即使在IF阴性血清中也通过免疫印迹法检测到了抗角蛋白Abs。ELISA研究表明,IF滴度高的血清中抗角蛋白Abs水平也高。在使用含有U-Cyt-或B-Cyt-Abs的血清进行的IEM研究中,展示了两种不同的反应模式:U-Cyt-Abs染色基底上层角质形成细胞的张力丝,而B-Cyt-Abs则特异性地与基底细胞的张力丝反应。此外,SC-、U-Cyt-和G-Cyt-Abs被不溶性表皮蛋白吸收,吸收试验后B-Cyt-Abs的滴度降低。本研究提供了强有力的证据,表明大多数(尽管不是全部)人抗表皮Abs针对不同的角蛋白多肽,并且抗角蛋白Abs几乎普遍存在于所有人血清中。

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