School of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai 20093, China.
Shanghai Prajna Biology Technique Co.Ltd., Shangai 200433, China.
J Immunol Methods. 2021 Jul;494:113014. doi: 10.1016/j.jim.2021.113014. Epub 2021 Mar 19.
Unlike traditional immunoassay strips, a novel antigen immunechromatography fluorometric strip (AICFS) using inactivated bacterial antigen instead of an antibody as a test line and goat anti-mouse IgG-FITC as a tracer was developed. The applicability survey of AICFS indicated that E. coli O157:H7 (D3) and Acidovorax citrulli (6F) hybridoma cell cultures could be detected, but Vibrio parahemolyticus (H7, C9) hybridoma cell cultures were missed compared with the indirect enzyme-linked immunosorbent assay (ELISA). The four antibody affinity constants (Ka) were measured and compared, and AICFS could be suitable for high-affinity antibody detection. Compared with the traditional indirect ELISA, the AICFS sensitivity for D3 cell cultures, ascites, and purified antibodies was at least 2-fold more sensitive, the AICFS specific for D3 cell cultures by comparative interpretation was compliant except for the strain ATCC 43895, and the indirect ELISA missed it. More importantly, the AICFS method was confirmed by various real samples that it could be used in different scenarios regarding the antibody, including McAb preparation, the effective antibody use, and high-affinity antibody-secreted hybridoma auxiliary preparation and screening. It could be an excellent alternative method with less than 5% corresponding processing time for indirect ELISA method for pathogenic bacterial high-quality antibody detection. This is the first report of using AICFS for bacterial high-quality antibody detection and application in different samples, which demonstrates a rapid auxiliary tool for high-affinity antibody secreted-hybridoma screening and an excellent alternative method for high-quality antibody application.
与传统的免疫层析条相比,本研究开发了一种新型的抗原免疫层析荧光条(AICFS),该条使用灭活的细菌抗原代替抗体作为检测线,用山羊抗小鼠 IgG-FITC 作为示踪剂。AICFS 的适用性调查表明,该方法可以检测到大肠杆菌 O157:H7(D3)和酸蚀醋酸菌(6F)杂交瘤细胞培养物,但与间接酶联免疫吸附试验(ELISA)相比,未能检测到副溶血性弧菌(H7、C9)杂交瘤细胞培养物。测量并比较了四种抗体亲和力常数(Ka),结果表明 AICFS 适用于高亲和力抗体的检测。与传统的间接 ELISA 相比,AICFS 对 D3 细胞培养物、腹水和纯化抗体的检测灵敏度至少提高了 2 倍,通过比较解读,AICFS 对 D3 细胞培养物的特异性除了 ATCC 43895 菌株外均符合要求,而间接 ELISA 则未能检测到该菌株。更重要的是,通过各种实际样本验证了 AICFS 方法的有效性,该方法可用于不同场景下的抗体检测,包括 McAb 制备、有效抗体使用以及高亲和力抗体分泌杂交瘤辅助制备和筛选。它可以作为一种极好的替代方法,与间接 ELISA 方法相比,处理时间不到 5%,用于检测致病菌的高质量抗体。这是首次报道使用 AICFS 进行细菌高质量抗体检测和在不同样本中的应用,证明了该方法是一种快速的辅助工具,可用于筛选高亲和力抗体分泌杂交瘤,也是高质量抗体应用的一种极好的替代方法。