Giegerich G, Pette M, Meinl E, Epplen J T, Wekerle H, Hinkkanen A
Department of Neuroimmunology, Max-Planck Institute for Psychiatry, Martinsried.
Eur J Immunol. 1992 Mar;22(3):753-8. doi: 10.1002/eji.1830220319.
T cell receptor (TcR) alpha and beta nucleotide sequences involved in the human autoreactivity to myelin basic protein (MBP) were studied by screening cDNA libraries derived from 11 independent T lymphocyte clones (TCC) established from multiple sclerosis patients and healthy donors. The TCC with defined MBP peptide specificity and HLA-DR restriction expressed multiple TcR. Even TCC recognizing the same human MBP peptide [amino acids (aa) 139-153] in identical or very similar HLA-DR context expressed diverse TcR. Two TCC which recognized peptide aa 139-153 equally well in the context of both HLA-DR2a and -DR1 molecules used distinct TcR alpha but identical beta chains. The knowledge of TcR beta and TcR alpha chain sequences of human MBP-specific T cells will allow studies correlating structure and function of TcR and their targets in MBP autoreactivity. This may have an impact on the development of immunotherapies in multiple sclerosis.
通过筛选来自多发性硬化症患者和健康供体的11个独立T淋巴细胞克隆(TCC)构建的cDNA文库,研究了参与人类对髓鞘碱性蛋白(MBP)自身反应性的T细胞受体(TcR)α和β核苷酸序列。具有明确MBP肽特异性和HLA - DR限制性的TCC表达多种TcR。即使在相同或非常相似的HLA - DR背景下识别相同人类MBP肽[氨基酸(aa)139 - 153]的TCC也表达不同的TcR。在HLA - DR2a和 - DR1分子背景下均能同等良好地识别肽aa 139 - 153的两个TCC使用了不同的TcRα链但β链相同。了解人类MBP特异性T细胞的TcRβ和TcRα链序列将有助于研究TcR的结构与功能及其在MBP自身反应性中的靶点之间的关系。这可能会对多发性硬化症免疫疗法的发展产生影响。