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通过注射含镍的纯化蛋白衍生物,使经分枝杆菌免疫的豚鼠对镍产生致敏作用。

Induced sensitization to nickel in guinea pigs immunized with mycobacteria by injection of purified protein derivative with nickel.

作者信息

Kitaura H, Nakao N, Yoshida N, Yamada T

机构信息

Division of Orthodontic, Department of Developmental and Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852-8588, Japan.

出版信息

New Microbiol. 2003 Jan;26(1):101-8.

Abstract

Nickel has been reported to be one of the most common causes of allergic contact dermatitis. Despite the fact that nickel is a frequent sensitizer in humans, establishing animal models for nickel allergy has met with considerable difficulties. In clinical cases, allergic contact hypersensitivity to nickel develops much more readily in inflamed skin than normal skin. In this study, we tried to induce nickel sensitization when inflammation has been evoked in guinea pigs immunized with mycobacteria followed by co-administration of a mycobacterial component with nickel. We first examined the delayed-type hypersensitivity (DTH) reaction of mycobacterial components such as the cell wall, cell membrane, 70S ribosomal fraction, cytoplasm, tuberculin purified protein derivative (PPD), RNA and DNA from Mycobacterium bovis BCG in guinea pigs immunized with live M. bovis BCG or heat killed M. tuberculosis. When PPD was used, the hypersensitivity reaction was strongest. Next, we tested whether PPD with nickel could induce nickel sensitivity in guinea pigs immunized with mycobacteria. Strong sensitization to nickel was achieved by injecting PPD with nickel. However, if too large an amount of PPD or nickel salts was used, sensitization to nickel decreased. In this way, sensitization of nickel developed much more easily in guinea pigs immunized with mycobacteria by injection of an appropriate amount of nickel at the inflammation site induced by a suitable amount of PPD.

摘要

据报道,镍是过敏性接触性皮炎最常见的病因之一。尽管镍是人类常见的致敏原,但建立镍过敏动物模型却遇到了相当大的困难。在临床病例中,镍过敏性接触超敏反应在炎症皮肤中比正常皮肤更容易发生。在本研究中,我们试图在用分枝杆菌免疫的豚鼠诱发炎症后,通过将分枝杆菌成分与镍共同给药来诱导镍致敏。我们首先检测了分枝杆菌成分(如细胞壁、细胞膜、70S核糖体组分、细胞质、结核菌素纯化蛋白衍生物(PPD)、卡介苗的RNA和DNA)对用活卡介苗或热灭活结核分枝杆菌免疫的豚鼠的迟发型超敏反应(DTH)。当使用PPD时,超敏反应最强。接下来,我们测试了含镍PPD是否能在分枝杆菌免疫的豚鼠中诱导镍敏感性。通过注射含镍PPD实现了对镍的强烈致敏。然而,如果使用过多的PPD或镍盐,对镍的致敏性会降低。通过这种方式,在用分枝杆菌免疫的豚鼠中,通过在适量PPD诱导的炎症部位注射适量镍,镍致敏更容易发生。

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