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辅助性T细胞表位增强了用MHC I类限制性疟疾肽免疫的小鼠的细胞毒性反应。

T helper epitopes enhance the cytotoxic response of mice immunized with MHC class I-restricted malaria peptides.

作者信息

Widmann C, Romero P, Maryanski J L, Corradin G, Valmori D

机构信息

Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.

出版信息

J Immunol Methods. 1992 Oct 19;155(1):95-9. doi: 10.1016/0022-1759(92)90275-x.

Abstract

We have previously derived MHC class I (H-2Kd) restricted cytotoxic T lymphocytes (CTL) from BALB/c mice immunized with irradiated sporozoites from Plasmodium (P.) berghei and P. yoelii. The CTL recognize synthetic peptides corresponding to a region of the circumsporozoite (CS) protein that is homologous in the two species. In the present study, we have attempted to induce CS-specific CTL by immunization with those peptides in incomplete Freund's adjuvant. Only a low level CTL response was detected in BALB/c mice immunized with synthetic peptides corresponding to the Pb or Py CTL epitopes. In contrast, CS-specific CTL responses could be readily detected in mice injected with mixtures of peptides that combined the P. berghei or P. yoelii CTL epitopes with previously defined T helper epitopes. Several different T helper epitopes were shown to enhance the response when injected as separate peptides in a mixture, or when covalently linked to a CTL epitope. These results may have general implications for the elicitation of CTL responses to defined CTL epitopes and for the design of peptide-based synthetic vaccines.

摘要

我们之前已从用伯氏疟原虫和约氏疟原虫的辐照子孢子免疫的BALB/c小鼠中获得了主要组织相容性复合体I类(H-2Kd)限制性细胞毒性T淋巴细胞(CTL)。这些CTL识别与两种疟原虫环子孢子(CS)蛋白中同源区域相对应的合成肽。在本研究中,我们尝试用这些肽在不完全弗氏佐剂中免疫诱导CS特异性CTL。在用对应于伯氏疟原虫或约氏疟原虫CTL表位的合成肽免疫的BALB/c小鼠中,仅检测到低水平的CTL应答。相反,在注射了将伯氏疟原虫或约氏疟原虫CTL表位与先前确定的T辅助表位组合的肽混合物的小鼠中,可容易地检测到CS特异性CTL应答。当以混合物中的单独肽形式注射,或与CTL表位共价连接时,几种不同的T辅助表位显示出可增强应答。这些结果可能对引发针对确定的CTL表位的CTL应答以及基于肽的合成疫苗的设计具有普遍意义。

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