Rudolph D L, Khabbaz R F, Folks T M, Lal R B
Retrovirus Diseases Branch, Centers for Disease Control, Atlanta, Georgia 30333.
Diagn Microbiol Infect Dis. 1993 Jul;17(1):35-9. doi: 10.1016/0732-8893(93)90067-h.
Two recombinant fusion proteins representing the C-terminus of the envelope glycoprotein of HTLV-I (rEnv-93(201-440)) and the C-terminus of the external glycoprotein (RE-3(165-306)) were tested in a Western blot (WB) assay for their ability to detect the presence of env antibodies in serum specimens from HTLV-I (n = 27) and HTLV-II (n = 22) infected individuals. The rEnv-93 reacted with 27 (100%) of 27 HTLV-I-infected specimens and 19 (86%) of 22 of HTLV-II-infected specimens. In contrast, RE-3 reacted with 25 (93%) of 27 HTLV-I-infected specimens, and only six (27%) of 22 HTLV-II-infected specimens, thus demonstrating predominant reactivity with HTLV-I compared with HTLV-II. Because of the high sensitivity of rEnv-93 reactivity in both HTLV-I and HTLV-II, the specificity of this env protein was evaluated in specimens with isolated gag reactivity (HTLVind). Of the 44 HTLVind specimens, four (9%) demonstrated reactivity to rEnv-93 in WB assay. We, therefore, conclude that although rEnv-93 is highly sensitive for detection of env protein, it has the potential to yield some false-positive reactions presumably due to the conserved nature of retroviral transmembrane epitopes.
在蛋白质免疫印迹(WB)试验中,对两种重组融合蛋白进行了检测,这两种蛋白分别代表人类嗜T淋巴细胞病毒I型(HTLV-I)包膜糖蛋白的C端(rEnv-93(201-440))和外膜糖蛋白的C端(RE-3(165-306)),以评估它们检测HTLV-I感染个体(n = 27)和HTLV-II感染个体(n = 22)血清标本中env抗体的能力。rEnv-93与27份HTLV-I感染标本中的27份(100%)以及22份HTLV-II感染标本中的1