Yahata G
Department of Obstetrics and Gynecology, Niigata University School of Medicine.
Nihon Sanka Fujinka Gakkai Zasshi. 1992 Jun;44(6):695-702.
In recent years, human papillomavirus (HPV) infection in female genital organs has attracted increasing attention because of its association with lesions in the uterine cervix, especially cervical carcinoma. In this study, the author attempted to determine the presence or absence of HPV infection in the cervical region by means of the polymerase chain reaction (PCR) method, which has become practical thanks to the development of thermostable DNA polymerase, and compared this method with traditional Southern blotting. Moreover, we conducted PCR after detecting DNA by two methods: target punch biopsy and cervicovaginal lavage, and compared the results in terms of detection. 1. The results of HPV detection from the isolated tissue were compared with those of traditional Southern blotting and PCR combined with subsequent hybridization under high stringency (PCR-H). Among the cases that showed negative response with the former method, two of six specimens of cervical carcinoma tissue, and four of eight specimens of normal cervical tissue yielded a positive response as a result of hybridization under low stringency after PCR (PCR-L). HPV was investigated in 56 clinical specimens by PCR. PCR-L was positive in 50.0% and 20.0% of the specimens of cervical carcinoma and normal cervical tissue, respectively. With PCR-H, the positive rates were 37.5% and 7.5% in cervical carcinoma and normal cervical tissue, respectively. 2. Among CIN patients who were followed up at the outpatient clinic, PCR was conducted in specimens obtained by cervicovaginal lavage and target punch biopsy, and the rates of HPV detection were compared.(ABSTRACT TRUNCATED AT 250 WORDS)
近年来,女性生殖器官的人乳头瘤病毒(HPV)感染因其与子宫颈病变尤其是宫颈癌的关联而受到越来越多的关注。在本研究中,作者尝试借助聚合酶链反应(PCR)方法来确定宫颈区域是否存在HPV感染,由于耐热DNA聚合酶的发展,该方法已变得切实可行,并且将此方法与传统的Southern印迹法进行了比较。此外,我们通过两种方法检测DNA后进行PCR:目标打孔活检和宫颈阴道灌洗,并在检测方面比较了结果。1. 将从分离组织中检测HPV的结果与传统Southern印迹法以及PCR结合随后的高严谨度杂交(PCR-H)的结果进行比较。在前者方法显示阴性反应的病例中,6份宫颈癌组织标本中的2份以及8份正常宫颈组织标本中的4份在PCR后低严谨度杂交(PCR-L)时产生了阳性反应。通过PCR对56份临床标本进行了HPV检测。PCR-L在宫颈癌标本和正常宫颈组织标本中的阳性率分别为50.0%和20.0%。采用PCR-H时,宫颈癌和正常宫颈组织中的阳性率分别为37.5%和7.5%。2. 在门诊随访的CIN患者中,对通过宫颈阴道灌洗和目标打孔活检获得的标本进行PCR,并比较HPV检测率。(摘要截断于250字)