Swan D C, Tucker R A, Tortolero-Luna G, Mitchell M F, Wideroff L, Unger E R, Nisenbaum R A, Reeves W C, Icenogle J P
National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Atlanta, Georgia 30333, USA.
J Clin Microbiol. 1999 Apr;37(4):1030-4. doi: 10.1128/JCM.37.4.1030-1034.1999.
The association between human papillomavirus (HPV) DNA copy number and cervical disease was investigated. Viral DNA copy number for the most common high-risk HPV types in cervical cancer (types 16, 18, 31, and 45) was determined in cervical cytobrush specimens from 149 women with high-grade cervical intraepithelial neoplasias (CIN II-CIN III), 176 with low-grade CIN (CIN I), and 270 with normal cytology. Quantitative, PCR-based fluorescent assays for each of the HPV genotypes and for the beta-globin gene were used. The amount of cellular DNA increased significantly with increasing disease; thus, HPV was expressed as copies per microgram of cellular DNA. The assay had a dynamic range of >10(7), allowing documentation for the first time of the wide range of HPV copy numbers seen in clinical specimens. Median HPV DNA copy number varied by more than 10(4) among the viral types. HPV16 was present in the highest copy number; over 55% of HPV16-positive samples contained more than 10(8) copies/microgram. Median copy number for HPV16 showed dramatic increases with increasing epithelial abnormality, an effect not seen with the other HPV types. HPV16 increased from a median of 2.2 x 10(7) in patients with normal cytology, to 4.1 x 10(7) in CIN I patients, to 1.3 x 10(9) copies/microgram in CIN II-III patients. Even when stratified by cervical disease and viral type, the range of viral DNA copies per microgram of cellular DNA was quite large, precluding setting a clinically significant cutoff value for "high" copy numbers predictive of disease. This study suggests that the clinical usefulness of HPV quantitation requires reassessment and is assay dependent.
研究了人乳头瘤病毒(HPV)DNA拷贝数与宫颈疾病之间的关联。在149例高级别宫颈上皮内瘤变(CIN II - CIN III)、176例低级别CIN(CIN I)以及270例细胞学正常的女性宫颈细胞刷标本中,测定了宫颈癌中最常见的高危HPV类型(16、18、31和45型)的病毒DNA拷贝数。采用基于PCR的针对每种HPV基因型以及β - 珠蛋白基因的定量荧光检测法。细胞DNA的量随着疾病程度加重而显著增加;因此,HPV以每微克细胞DNA的拷贝数来表示。该检测方法的动态范围大于10⁷,首次记录了临床标本中所见的广泛HPV拷贝数范围。病毒类型之间HPV DNA拷贝数中位数相差超过10⁴。HPV16的拷贝数最高;超过55%的HPV16阳性样本每微克含有超过10⁸个拷贝。HPV16的拷贝数中位数随着上皮异常程度的增加而显著升高,其他HPV类型未见此效应。HPV16从细胞学正常患者的中位数2.2×10⁷,增加到CIN I患者的4.1×10⁷,再到CIN II - III患者的1.3×10⁹拷贝/微克。即使按宫颈疾病和病毒类型分层,每微克细胞DNA的病毒DNA拷贝数范围仍然很大,无法设定一个具有临床意义的“高”拷贝数临界值来预测疾病。这项研究表明,HPV定量检测的临床实用性需要重新评估,且依赖于检测方法。