Taibi A, Guevara-Espinoza A, Schöneck R, Yahiaoui B, Ouaissi A
Centre d'Immunologie et de Biologie Parasitaire, Unité INSERM U415, Institut Pasteur, Lille, France.
Parasitology. 1995 Dec;111 ( Pt 5):581-90. doi: 10.1017/s0031182000077064.
In the present study, the diagnostic value of Trypanosoma cruzi recombinant protein (Tc24) was examined. Although antibodies against Tc24 were detected during natural and experimental T. cruzi infections, specificity studies revealed that sera from T. rangeli-infected mice also recognized to some extent Tc24 protein. In addition, sera from Tc24-immunized mice reacted against a 21 kDa polypeptide in T. rangeli extracts. Detailed analysis of the antibody response against 20-40 peptide localized in the Tc24 amino-terminal domain suggests that this sequence is not expressed by T. rangeli 21 kDa antigen. Therefore, the PCR reaction using oligonucleotides corresponding to a 20-26 peptide clearly demonstrated the specificity of the oligoprobes for T. cruzi identification. Positive signals were also found when using blood samples from T. cruzi-infected mice. Taken together, these results suggest that the PCR-based 20-26 assay may be useful in the specific diagnosis of Chagas' disease.
在本研究中,检测了克氏锥虫重组蛋白(Tc24)的诊断价值。尽管在自然和实验性克氏锥虫感染期间检测到了针对Tc24的抗体,但特异性研究表明,感染兰氏锥虫的小鼠血清也在一定程度上识别Tc24蛋白。此外,来自用Tc24免疫的小鼠的血清与兰氏锥虫提取物中的一种21 kDa多肽发生反应。对针对位于Tc24氨基末端结构域的20 - 40肽的抗体反应的详细分析表明,兰氏锥虫21 kDa抗原不表达该序列。因此,使用与20 - 26肽相对应的寡核苷酸进行的PCR反应清楚地证明了寡核苷酸探针用于鉴定克氏锥虫的特异性。当使用来自感染克氏锥虫的小鼠的血液样本时也发现了阳性信号。综上所述,这些结果表明基于PCR的20 - 26检测法可能有助于恰加斯病的特异性诊断。