Egami Yoko, Narushima Yuta, Ohshima Motohiro, Yoshida Akira, Yoneta Naruki, Masaki Yasufumi, Itoh Kunihiko
Department of Clinical Pharmacology & Genetics, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Division of Hematology and Immunology, Department of Internal Medicine, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Kahoku-gun, Ishikawa 920-0293, Japan.
J Biochem. 2018 Jan 1;163(1):61-68. doi: 10.1093/jb/mvx065.
CD antigens are well known as therapeutic targets of B-cell lymphoma. To isolate therapeutic antibodies that recognize novel targets other than CD antigens, we constructed a phage display combinatorial antibody Fab library from bone marrow lymphocytes of B-cell lymphoma patient. To eliminate antibodies reactive with known B-cell lymphoma antigen, non-hematopoietic and patient's sera reactive HeLaS3 cells was selected as a target of whole cell panning. Five rounds of panning against live HeLaS3 cells retrieved single Fab clone, termed AHSA (Antibody to HeLa Surface Antigen). Using phage display random peptide library, LSYLEP was identified as an epitope sequence of AHSA. LC-MS/MS analysis of AHSA-precipitated HeLaS3 cell lysates detected several fragments corresponding to the sequence of chondroitin sulphate proteoglycan 4 (CSPG4) core protein. Since LSYLEP sequence was at the position of 313-318 of CSPG4, we considered that CSPG4 was AHSA-associated antigen. Double staining of CSPG4-postive MDA-MB-435S cells with AHSA and anti-CSPG4 rabbit antibody showed identical staining position, and reduced AHSA reactivity was observed in CSPG4-siRNA treated MDA-MB-435S cells. In conclusion, we retrieved a human Fab from antibody library of B-cell lymphoma patient, and identified CSPG4 as a recognizing antigen. AHSA may have potential benefits for development of CSPG4-targeting theranostics for B-cell lymphoma.
CD抗原作为B细胞淋巴瘤的治疗靶点广为人知。为了分离识别除CD抗原之外新靶点的治疗性抗体,我们从一名B细胞淋巴瘤患者的骨髓淋巴细胞构建了一个噬菌体展示组合抗体Fab文库。为了去除与已知B细胞淋巴瘤抗原反应的抗体,选择非造血细胞和患者血清反应性的HeLaS3细胞作为全细胞淘选的靶点。针对活的HeLaS3细胞进行了五轮淘选,获得了一个单Fab克隆,称为AHSA(抗HeLa表面抗原抗体)。使用噬菌体展示随机肽文库,鉴定出LSYLEP为AHSA的表位序列。对AHSA沉淀的HeLaS3细胞裂解物进行LC-MS/MS分析,检测到几个与硫酸软骨素蛋白聚糖4(CSPG4)核心蛋白序列相对应的片段。由于LSYLEP序列位于CSPG4的313 - 318位,我们认为CSPG4是与AHSA相关的抗原。用AHSA和抗CSPG4兔抗体对CSPG4阳性的MDA-MB-435S细胞进行双重染色,显示染色位置相同,并且在CSPG4-siRNA处理的MDA-MB-435S细胞中观察到AHSA反应性降低。总之,我们从B细胞淋巴瘤患者的抗体文库中获得了一种人Fab,并鉴定出CSPG4为识别抗原。AHSA可能对开发针对B细胞淋巴瘤的CSPG4靶向治疗诊断方法具有潜在益处。