Khusmith S, Intapan P, Tharavanij S, Tuntrakul S, Indravijit K A, Bunnag D
Department of Microbiology, Faculty of Tropical Medicine, Hospital for Tropical Diseases, Mahidol University, Bangkok, Thailand.
Southeast Asian J Trop Med Public Health. 1992 Dec;23(4):745-51.
Two systems of sandwich enzyme-linked immunosorbent assay (ELISA), a two-site monoclonal antibody sandwich ELISA MAb-MAb sandwich ELISA) and a two site polyclonal-monoclonal antibody sandwich ELISA (PAb-MAb sandwich ELISA) for the detection of Plasmodium vivax antigens were developed. The assays showed good correlation with the level of parasitemia when tested against serially diluted P. vivax parasites (r = 0.937, and 0.997 for MAb-MAb and PAb-MAb sandwich ELISA, respectively), with the ability to detect as few as 6.68 parasites/10(6) erythrocytes and 2.69 parasites/10(3) erythrocytes, respectively. The MAb-MAb sandwich ELISA was specific, since it was positive only with P. vivax-infected erythrocytes from vivax malaria patients and negative when erythrocytes from 34 healthy individuals and 30 falciparum malaria cases were tested. In contrast, cross-reaction was found in the PAb-MAb sandwich ELISA when the plates were coated with polyclonal IgG and tested against the serially diluted P. falciparum SO strain antigen prepared from in vitro cultures. Comparison between the two systems of two-site sandwich ELISA showed that the MAb-MAb sandwich ELISA was superior to the PAb-MAb sandwich ELISA: (1) it gave a higher sensitivity when tested with serially diluted P. vivax antigen preparations from vivax malaria patients; (2) it gave a higher specificity when tested with the SO strain of P. falciparum from in vitro cultures, (3) it gave a lower absorbance value when tested with erythrocytes from healthy individuals. All 281 cases of vivax malaria already proven by microscopic examination were positive by MAb-MAb sandwich ELISA.(ABSTRACT TRUNCATED AT 250 WORDS)
开发了两种夹心酶联免疫吸附测定(ELISA)系统,即双位点单克隆抗体夹心ELISA(MAb-MAb夹心ELISA)和双位点多克隆-单克隆抗体夹心ELISA(PAb-MAb夹心ELISA),用于检测间日疟原虫抗原。当用系列稀释的间日疟原虫寄生虫进行检测时,这些测定与寄生虫血症水平显示出良好的相关性(MAb-MAb和PAb-MAb夹心ELISA的r分别为0.937和0.997),分别能够检测低至6.68个寄生虫/10⁶个红细胞和2.69个寄生虫/10³个红细胞。MAb-MAb夹心ELISA具有特异性,因为它仅对间日疟患者的间日疟感染红细胞呈阳性,而对34名健康个体和30例恶性疟病例的红细胞进行检测时呈阴性。相比之下,当用多克隆IgG包被酶标板并针对从体外培养物中制备的系列稀释的恶性疟原虫SO株抗原进行检测时,在PAb-MAb夹心ELISA中发现了交叉反应。两种双位点夹心ELISA系统之间的比较表明,MAb-MAb夹心ELISA优于PAb-MAb夹心ELISA:(1)用间日疟患者的系列稀释间日疟原虫抗原制剂进行检测时,它具有更高的灵敏度;(2)用体外培养的恶性疟原虫SO株进行检测时,它具有更高的特异性;(3)用健康个体的红细胞进行检测时,它具有更低的吸光度值。所有281例经显微镜检查已确诊的间日疟病例,通过MAb-MAb夹心ELISA检测均为阳性。(摘要截断于250字)