Kiecker Felix, Streitz Mathias, Ay Bernhard, Cherepnev Georgy, Volk Hans-Dieter, Volkmer-Engert Rudolf, Kern Florian
Abteilung Klinische Immunologie, Institut für Medizinische Immunologie der Charité, Humboldt-Universität zu Berlin (Charité), Campus Charité Mitte, Berlin, Germany.
Hum Immunol. 2004 May;65(5):523-36. doi: 10.1016/j.humimm.2004.02.017.
The analysis of T-cell responses to peptides has recently become a busy area of immunologic research. Peptides may be used as single stimulants, pools or libraries, or as part of peptide/major histocompatibility complexes (MHC) for direct T-cell receptor staining. For stimulating T cells, peptides must be bound to MHC molecules. In this study we have used 9- or 10-amino acid peptides, 15-amino acid peptides containing stimulating shorter sequences, and peptides with modified C-terminal function. On average 67% of the T cells from healthy cytomegalovirus-positive donors that bound a frequently used cytomegalovirus pp65/HLA-A*0201 tetramer were able to produce interferon-gamma on stimulation with the respective 9-amino acid peptide. Peptides of 15 amino acids length used at the same concentration (in microg/ml) stimulated CD8 T cells somewhat less efficiently (on average 77% of the frequencies induced with the respective shorter peptides). Modifications of 9-amino acid peptides such as addition of amino acids or functional groups often resulted in a decreased ability to stimulate. However, based on our own results, published data, and theoretic considerations, we conclude that sets of peptides of 15 amino acids length with 11 amino acids overlap represent a good compromise for stimulating both CD8 and CD4 T cells in a number of applications. These parameters may be modified subject to the purpose of a study.
对肽的T细胞反应分析最近已成为免疫学研究的一个热门领域。肽可作为单一刺激物、肽池或肽库使用,或作为肽/主要组织相容性复合体(MHC)的一部分用于直接T细胞受体染色。为了刺激T细胞,肽必须与MHC分子结合。在本研究中,我们使用了9或10个氨基酸的肽、包含刺激活性较短序列的15个氨基酸的肽以及具有修饰C末端功能的肽。平均而言,来自健康巨细胞病毒阳性供体且与常用的巨细胞病毒pp65/HLA-A*0201四聚体结合的T细胞中,有67%在用相应的9个氨基酸肽刺激时能够产生干扰素-γ。相同浓度(以微克/毫升计)下使用的15个氨基酸长度的肽刺激CD8 T细胞的效率略低(平均为相应较短肽诱导频率的77%)。9个氨基酸肽的修饰,如添加氨基酸或官能团,往往会导致刺激能力下降。然而,基于我们自己的结果、已发表的数据和理论考虑,我们得出结论,在许多应用中,15个氨基酸长度且有11个氨基酸重叠的肽组是刺激CD8和CD4 T细胞的良好折衷方案。这些参数可根据研究目的进行修改。