Pornprasert Sakorn, Dettrairat Sakchai, Vongchan Preeyanat, Apichatpiyakul Chatchawan
Deparetment of Clinical Microscopy, Faculty of Associated Medical Sciences, Chiang Mai University, 110 Intawarorost Road, Mueang, Chiang Mai, 50200, Thailand.
Southeast Asian J Trop Med Public Health. 2005 Jul;36(4):966-9.
Monoclonal antibody against P. mameffei yeast secreted antigen was produced in order to develop a serological test for penicilliosis marneffei. The yeast form of P. marneffei was cultured in brain heart infusion broth at 37 degrees C for 7 days. A secreted antigen was prepared, partially purified from culture supernatant and subsequently immunized in a BALB/c mouse. Mouse monoclonal antibody was produced from immune spleen cells by a standard hybridoma technique. Specificity of the obtained monoclonal antibody was assessed with yeast secreted antigens for P. mameffei, C. alblicans, C. neoformans, and H. capsulatum by an indirect ELISA. Three of 46 hybrid clones (1 F1, 2G5, and 3G4) reacted positively with P mameffei secreted antigen. 1 F1 and 3G4 were cloned by two rounds of limiting dilution. Partially purified monoclonal antibody and rabbit polyclonal antibody against P. marneffei yeast secreted antigen were used to develop a double antibody sandwich ELISA to detect P. marneffei antigen in plasma or serum samples of 7 patients with penicilliosis marneffei and 5 healthy controls. The sandwich ELISA developed using monoclonal antibody as a capture antibody and rabbit polyclonal antibody as a detector was able to detect P. marneffei antigen in all the plasma and serum samples of penicilliosis marneffei patients, while negative in all the healthy controls. Thus, the monoclonal antibody produced in the present study appeared to be highly specific for P. marneffei and the double antibody sandwich ELISA developed using monoclonal and polyclonal antibodies against the yeast secreted antigen of P. marneffei showed a strong potential for the diagnosis of penicilliosis marneffei.
为了开发一种马尔尼菲青霉病的血清学检测方法,制备了抗马尔尼菲青霉酵母分泌抗原的单克隆抗体。马尔尼菲青霉的酵母形式在脑心浸液肉汤中于37℃培养7天。制备分泌抗原,从培养上清液中部分纯化,随后在BALB/c小鼠中进行免疫。通过标准杂交瘤技术从免疫脾细胞中产生小鼠单克隆抗体。通过间接ELISA用马尔尼菲青霉、白色念珠菌、新型隐球菌和荚膜组织胞浆菌的酵母分泌抗原评估所获得单克隆抗体的特异性。46个杂交克隆中的3个(1F1、2G5和3G4)与马尔尼菲青霉分泌抗原呈阳性反应。通过两轮有限稀释对1F1和3G4进行克隆。使用部分纯化的单克隆抗体和抗马尔尼菲青霉酵母分泌抗原的兔多克隆抗体开发双抗体夹心ELISA,以检测7例马尔尼菲青霉病患者和5名健康对照的血浆或血清样本中的马尔尼菲青霉抗原。以单克隆抗体作为捕获抗体、兔多克隆抗体作为检测抗体开发的夹心ELISA能够检测所有马尔尼菲青霉病患者的血浆和血清样本中的马尔尼菲青霉抗原,而所有健康对照均为阴性。因此,本研究中产生的单克隆抗体似乎对马尔尼菲青霉具有高度特异性,并且使用针对马尔尼菲青霉酵母分泌抗原的单克隆和多克隆抗体开发的双抗体夹心ELISA在马尔尼菲青霉病的诊断中显示出强大的潜力。