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在小鼠和人类中,针对巴西副球孢子菌主要抗原成分gp43的免疫反应中独特型调节的证据。

Evidence of idiotypic modulation in the immune response to gp43, the major antigenic component of Paracoccidioides brasiliensis in both mice and humans.

作者信息

Souza A R, Gesztesi J L, Moraes J Z, Cruz C R, Sato J, Mariano M, Lopes J D

机构信息

Microbiology, Immunology and Parasitology Department, Federal University of São Paulo (UNIFESP), Brazil.

出版信息

Clin Exp Immunol. 1998 Oct;114(1):40-8. doi: 10.1046/j.1365-2249.1998.00679.x.

Abstract

Paracoccidioidomycosis (PCM) is a systemic mycosis endemic in Latin America, with a high prevalence in Brazil, Argentina, Colombia and Venezuela. The aetiologic agent of disease is a thermal dimorphic fungus, Paracoccidioides brasiliensis. A glycoprotein of 43,000 D (gp43) is the major antigen of P. brasiliensis. Antibodies directed to this antigen are detected in the sera of all patients with PCM. Gp43 binds to laminin, thus participating in adhesion, invasion and pathogenesis of the fungus. As the role of antibodies in PCM is not fully understood, we decided to investigate the outcome of mice immunization with three distinct anti-gp43 MoAbs (17c, 8a and 24a) coupled with keyhole limpet haemocyanin (KLH). Results show not only the expected presence of anti-Id (AB2) antibodies in the sera of these animals but also a spontaneous and increasing amount of anti-anti-Id (AB3) antibodies after the third course of immunization. Hybridomas producing both AB2 and AB3 MoAbs were obtained using spleen cells from mice immunized with MoAb 17c. AB3 MoAbs were also obtained with spleen cells of mice immunized with MoAbs 8a and 24a. It was also shown that human PCM patients' sera with high titres of anti-gp43 antibodies generate anti-Id antibodies. These data suggest that the immune response to P. brasiliensis can be spontaneously modulated by the idiotypic network.

摘要

副球孢子菌病(PCM)是一种在拉丁美洲流行的系统性真菌病,在巴西、阿根廷、哥伦比亚和委内瑞拉发病率很高。该病的病原体是一种嗜热双相真菌,巴西副球孢子菌。一种43000D的糖蛋白(gp43)是巴西副球孢子菌的主要抗原。在所有PCM患者的血清中都能检测到针对该抗原的抗体。Gp43与层粘连蛋白结合,从而参与真菌的黏附、侵袭和发病机制。由于抗体在PCM中的作用尚未完全了解,我们决定研究用三种不同的抗gp43单克隆抗体(17c、8a和24a)与钥孔戚血蓝蛋白(KLH)偶联免疫小鼠的结果。结果显示,这些动物的血清中不仅预期存在抗独特型(AB2)抗体,而且在第三次免疫后自发产生且数量不断增加的抗抗独特型(AB3)抗体。使用用单克隆抗体17c免疫的小鼠的脾细胞获得了产生AB2和AB3单克隆抗体的杂交瘤。用单克隆抗体8a和24a免疫的小鼠的脾细胞也获得了AB3单克隆抗体。还表明,具有高滴度抗gp43抗体的人类PCM患者血清会产生抗独特型抗体。这些数据表明,对巴西副球孢子菌的免疫反应可由独特型网络自发调节。

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