Liu Ying, Zhu Ping, Hu Ya-mei
Department of Hematology, Peking University First Hospital, Beijing 100034, China.
Zhonghua Yi Xue Za Zhi. 2004 Jan 17;84(2):97-102.
To identify that immunoglobulin heavy chain framework regions-derived peptides function as cytotoxic T lymphocytes epitopes.
Seven IgHV gene families were respectively amplified by PCR and directly sequenced for 108 acute lymphoblastic leukemia cases. Sequences available were translated into amino acid sequences. Bioinformatics were applied for analyzing recombination patterns and gene mutations of the IgHV genes. Softwares SYFPEITHI and BIMAS were used for predicting the T cell epitopes in the immunoglobulin heavy chain variable regions. To determine whether the predicted peptides have immunogenicity, a IgHV1 family nonapeptide QLVQSGAEV was synthesized as a representation and T2 binding assay of this peptide was performed, inducing proliferation of T cells from normal HLA-A * 0201 peripheral blood lymphocytes (PBLs) with QLVQSGAEV-loaded antigen presenting cells, and detecting the proliferating T cells by HLA-A * 0201/QLVQSGAEV tetramers.
Complete IgHV gene rearrangements were identified in 66% cases. Among 40 B-ALL IgHV sequences available, 26 were predicted for antigenic nonapeptides that are likely to bind to HLA-A * 0201 molecule. Twelve peptides were acquired. Except one peptide derived from CDR3, 10 (83%) peptides were located in the immunoglobulin heavy chain framework regions. Moreover B-ALL belonging to the same IgHV family shared 1 - 2 peptides. Synthesized peptide QLVQSGAEV up-regulated HLA-A * 0201 expression 1.63 times on T2 cell surface. PBLs from a normal HLA-A * 0201 donor were stimulated with QLVQSGAEV-loaded autologous PBMCs and T2, the CD8(+) tetramer(+) cells in gated lymphocyte population increased from 1.64% after the first stimulation to 82.57% after the third stimulation.
Immunoglobulin heavy chain framework region genes encode IgHV family-specific peptides recognized by CTLs. Specific CTLs remain in human peripheral T cell repertoire. Immunoglobulin heavy chain framework-derived peptides function as T cell epitopes to induce the proliferation of specific CTLs.
鉴定免疫球蛋白重链框架区衍生肽作为细胞毒性T淋巴细胞表位的功能。
采用聚合酶链反应(PCR)分别扩增108例急性淋巴细胞白血病病例的7个IgHV基因家族,并直接进行测序。将获得的序列翻译成氨基酸序列。应用生物信息学分析IgHV基因的重组模式和基因突变。使用SYFPEITHI和BIMAS软件预测免疫球蛋白重链可变区的T细胞表位。为确定预测的肽是否具有免疫原性,合成了一个IgHV1家族九肽QLVQSGAEV作为代表,并进行该肽的T2结合试验,用负载QLVQSGAEV的抗原呈递细胞诱导正常HLA-A * 0201外周血淋巴细胞(PBL)的T细胞增殖,并用HLA-A * 0201/QLVQSGAEV四聚体检测增殖的T细胞。
66%的病例鉴定出完整的IgHV基因重排。在40个可获得的B-ALL IgHV序列中,26个被预测为可能与HLA-A * 0201分子结合的抗原性九肽。获得了12个肽。除一个来源于互补决定区3(CDR3)的肽外,10个(83%)肽位于免疫球蛋白重链框架区。此外,属于同一IgHV家族的B-ALL共享1 - 2个肽。合成肽QLVQSGAEV使T2细胞表面HLA-A * 0201表达上调1.63倍。用负载QLVQSGAEV的自体PBMC和T2刺激正常HLA-A * 0201供体的PBL,门控淋巴细胞群体中CD8(+)四聚体(+)细胞从第一次刺激后的1.64%增加到第三次刺激后的82.57%。
免疫球蛋白重链框架区基因编码可被细胞毒性T淋巴细胞识别的IgHV家族特异性肽。特异性细胞毒性T淋巴细胞存在于人类外周T细胞库中。免疫球蛋白重链框架区衍生肽作为T细胞表位发挥功能,诱导特异性细胞毒性T淋巴细胞增殖。