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来自巴拿马的克氏锥虫低毒力克隆株的免疫寄生虫学研究:实验感染小鼠中针对罗氏锥虫的体液免疫反应和抗原交叉反应

Immunoparasitological studies of Trypanosoma cruzi low virulence clones from Panama: humoral immune responses and antigenic cross-reactions with Trypanosoma rangeli in experimentally infected mice.

作者信息

Saldaña A, Sousa O E, Orn A

机构信息

Center for Research and Diagnosis of Parasitic Diseases (CIDEP), Faculty of Medecine, University of Panama, Panama.

出版信息

Scand J Immunol. 1995 Dec;42(6):644-50. doi: 10.1111/j.1365-3083.1995.tb03707.x.

Abstract

The kinetics of humoral immune responses were investigated in mice experimentally infected with five clones of Trypanosoma cruzi isolated from different sources in Panama. Sera were collected at different timepoints post-infection. ELISA and IHA tests were used to detect antibodies against T. cruzi epimastigote antigens. The levels of T. cruzi specific antibodies increased during the course of infection; at day 90 post-infection the range was between 1:5120 and 1:10240. A high correlation was evident between ELISA and IHA results. Western blots revealed that these antibodies recognized polypeptides of 81, 76 and 71 KDa during the first weeks and 81, 76, 71, 50, 40, 28 and 12 KDa after 30-50 days. Only minor differences in antigen recognition patterns were demonstrated, suggesting that the major antigens may be represented in all clones. T. rangeli antigens were also recognized by T. cruzi seropositive sera. However, an ELISA test using antigens isolated from a genomic expression library of T. cruzi revealed that a hyperimmune rabbit serum against T. rangeli was unable to recognize the repeat sequence of SAPA (Shed Acute Phase Antigen) peptides but did recognize a number of other T. cruzi synthetic peptide antigens. The importance of these findings, in the context of Chagas' disease, is discussed.

摘要

在实验感染了从巴拿马不同来源分离出的五个克氏锥虫克隆的小鼠中,研究了体液免疫反应的动力学。在感染后的不同时间点收集血清。采用酶联免疫吸附测定(ELISA)和间接血凝试验(IHA)检测抗克氏锥虫前鞭毛体抗原的抗体。克氏锥虫特异性抗体水平在感染过程中升高;感染后第90天,范围在1:5120至1:10240之间。ELISA和IHA结果之间存在高度相关性。蛋白质印迹法显示,这些抗体在最初几周识别81、76和71千道尔顿的多肽,30 - 50天后识别81、76、71、50、40、28和12千道尔顿的多肽。仅显示出抗原识别模式的微小差异,表明所有克隆中可能都存在主要抗原。克氏锥虫血清阳性血清也识别兰氏锥虫抗原。然而,使用从克氏锥虫基因组表达文库中分离的抗原进行的ELISA试验表明,针对兰氏锥虫的超免疫兔血清无法识别Shed急性期抗原(SAPA)肽的重复序列,但确实识别了许多其他克氏锥虫合成肽抗原。本文讨论了这些发现对于恰加斯病的重要性。

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