Bernard C, Mougin C, Bettinger D, Didier J M, Lab M
Laboratoire de Virologie, CHU Saint-Jacques, Besançon.
Mol Cell Probes. 1994 Oct;8(5):337-43. doi: 10.1006/mcpr.1994.1049.
The efficiency of the in situ polymerase chain reaction (PCR) for the detection of human papillomavirus (HPV) DNA sequences in 20 cervical biopsies fixed with buffered formalin, paraffin-embedded and revealed negatively by conventional in situ hybridization (ISH) has been investigated. The biopsies were classified histologically into condylomata acuminata without dysplasia, cervical intraepithelial neoplasia and carcinoma in situ. Amplified HPV DNA was performed after an optimal proteolytic digestion using one pair of consensus oligonucleotide primers located in the L1 ORF of HPV 6 and ISH was carried out after the PCR assay with a cocktail of biotinylated HPV probes. Viral DNA was detected in 100% of high grade squamous intraepithelial lesions (SIL) and in 50 to 60% of low grade SIL. The high sensitivity of the in situ PCR applicable to paraffin-embedded archival biopsies facilitated the detection of cells poorly reactive by conventional ISH. In situ PCR appeared clearly an efficient tool to investigate HPV infection in tissue sections.
研究了原位聚合酶链反应(PCR)检测20例经缓冲福尔马林固定、石蜡包埋且传统原位杂交(ISH)呈阴性的宫颈活检组织中人乳头瘤病毒(HPV)DNA序列的效率。活检组织经组织学分类为无发育异常的尖锐湿疣、宫颈上皮内瘤变和原位癌。使用位于HPV 6的L1开放阅读框中的一对共有寡核苷酸引物进行最佳蛋白水解消化后进行HPV DNA扩增,并在PCR检测后用生物素化HPV探针混合物进行ISH。在100%的高级别鳞状上皮内病变(SIL)和50%至60%的低级别SIL中检测到病毒DNA。适用于石蜡包埋存档活检组织的原位PCR的高灵敏度有助于检测传统ISH反应性差的细胞。原位PCR显然是研究组织切片中HPV感染的有效工具。