Singh-Naz N, Rodriguez W J, Kidd A H, Brandt C D
Department of Infectious Diseases, Children's Hospital National Medical Center, Washington, D.C.
J Clin Microbiol. 1988 Feb;26(2):297-300. doi: 10.1128/jcm.26.2.297-300.1988.
Monoclonal antibody specific for subgroup F enteric adenoviruses (EAds) was prepared by fusing P3-NS1/Ag4-1 mouse myeloma cells with lymphocytes from BALB/c mice immunized with G1105, an adenovirus type 41 (Ad41) strain. Monoclone 3F11/2H9, which specifically recognized Ad41, was successfully used as detector antibody in an enzyme-linked immunosorbent assay (ELISA). Additionally, previously prepared monoclones 5D8/2C2 and 2H6/1E11, recognizing Ad40 plus Ad41 and Ad40 alone, respectively, were used to study stool and/or tissue culture specimens from 106 patients with adenovirus-positive gastroenteritis. By ELISA, 91 had EAds (22 were Ad40 and 69 were Ad41) and 15 had non-EAds. ELISA results were in concordance with restriction endonuclease results for 38 of 39 specimens, with dot blot data for 19 of 20 specimens, and with neutralization test results for 74 of 78 specimens. ELISA was at least 10-fold more sensitive than direct electron microscopy was for the detection of EAds in stool specimens.
通过将P3-NS1/Ag4-1小鼠骨髓瘤细胞与用41型腺病毒(Ad41)毒株G1105免疫的BALB/c小鼠的淋巴细胞融合,制备了针对F亚群肠道腺病毒(EAds)的单克隆抗体。特异性识别Ad41的单克隆3F11/2H9成功用作酶联免疫吸附测定(ELISA)中的检测抗体。此外,先前制备的分别识别Ad40加Ad41和单独Ad40的单克隆5D8/2C2和2H6/1E11,用于研究106例腺病毒阳性肠胃炎患者的粪便和/或组织培养标本。通过ELISA检测,91例患者感染了EAds(22例为Ad40,69例为Ad41),15例感染了非EAds。ELISA结果与39份标本中的38份的限制性内切酶结果、20份标本中的19份的斑点印迹数据以及78份标本中的74份的中和试验结果一致。在粪便标本中检测EAds时,ELISA的灵敏度至少比直接电子显微镜高10倍。