Vretou E, Mentis A, Psarrou E, Tsoumaris L, Conidou G, Spiliopoulou D
Department of Biotechnology, Institut Pasteur Hellenique, Athens, Greece.
Sex Transm Dis. 1992 Mar-Apr;19(2):78-83.
Twenty-seven monoclonal antibodies (mAb), eight with subclass-specificities and nineteen reacting with one or two C. trachomatis serovars, were developed and used to immunotype twenty-six clinical isolates from Greek patients with chlamydial infections. Twelve samples, first classified as serovar D, were identified as the recently established serovar Da on the basis of their negative reaction with mAb JG9, an mAb previously shown to distinguish between D and Da, and a new mAb 114D9 with similar specificity. The 12 Da strains represent the highest prevalence of the rare serovar Da that has been reported worldwide. Further characterization of mAbs JG9 and 114D9 revealed a unique cross-reactivity of the D-specific JG9 with the mouse biovar MoPn. Epitope mapping studies on overlapping synthetic peptides of the fourth variable domain of the MOMP of serovar D and Da localized the epitopes of JG9 and 114D9 and a D/Da specific mAb 113D5 within this domain. The results were consistent with the specificity of these mAbs observed with whole microorganisms and indicated their usefulness as epidemiologic markers.
研制出了27种单克隆抗体(mAb),其中8种具有亚类特异性,19种与一两种沙眼衣原体血清型发生反应,并用于对来自希腊衣原体感染患者的26株临床分离株进行免疫分型。最初被归类为血清型D的12个样本,基于它们与mAb JG9(一种先前已证明可区分D和Da的单克隆抗体)以及具有相似特异性的新单克隆抗体114D9的阴性反应,被鉴定为最近确定的血清型Da。这12株Da菌株代表了全球范围内报道的罕见血清型Da的最高流行率。对单克隆抗体JG9和114D9的进一步表征揭示了D特异性JG9与小鼠生物变种MoPn的独特交叉反应性。对血清型D和Da的主要外膜蛋白(MOMP)第四可变结构域的重叠合成肽进行的表位作图研究,将JG9和114D9以及D/Da特异性单克隆抗体113D5的表位定位在该结构域内。结果与这些单克隆抗体对完整微生物观察到的特异性一致,并表明它们作为流行病学标志物的有用性。