Yoshioka M, Bixler G S, Atassi M Z
Mol Immunol. 1983 Oct;20(10):1133-7. doi: 10.1016/0161-5890(83)90123-2.
Recently, this laboratory has demonstrated that antibodies to preselected regions of a protein can be obtained by immunization with free small synthetic peptides (6-7 residues) without conjugation to a carrier. In the present work, we report the use of free synthetic peptides representing myoglobin (Mb) antigenic sites to prepare T-cell lines and clones of preselected specificities. Lymph node cells from mice primed in vivo with sperm-whale Mb were periodically passaged in vitro with synthetic peptide. After several passages, the peptide-driven long term T-cell cultures responded to the intact protein and exclusively to the peptide that was used to drive the cells. From these cultures, T-cell clones were prepared that responded only to the driving peptide and to the whole protein. The ability to prepare T-cell lines and T-cell clones with preselected submolecular specificities to a protein by driving cultures with desired synthetic peptides affords an important and simple tool for basic immunological investigations and for clinical applications.
最近,本实验室已证明,通过用游离的小合成肽(6 - 7个残基)进行免疫而无需与载体偶联,就可以获得针对蛋白质预选区域的抗体。在本研究中,我们报告了使用代表肌红蛋白(Mb)抗原位点的游离合成肽来制备具有预选特异性的T细胞系和克隆。用抹香鲸肌红蛋白在体内进行免疫的小鼠的淋巴结细胞,定期与合成肽在体外传代培养。经过几次传代后,由肽驱动的长期T细胞培养物对完整蛋白有反应,并且仅对用于驱动细胞的肽有反应。从这些培养物中制备了仅对驱动肽和全蛋白有反应的T细胞克隆。通过用所需的合成肽驱动培养物来制备对蛋白质具有预选亚分子特异性的T细胞系和T细胞克隆的能力,为基础免疫学研究和临床应用提供了一种重要且简单的工具。