Randhawa P S, Jaffe R, Faruki H, Rinaldo C R, Ho M, Demetris A J, Manez R, Kusne S, Ehrlich G D
Department of Pathology, Presbyterian University Hospital, Pittsburgh, Pennsylvania.
Mod Pathol. 1994 Jan;7(1):125-8.
A multiplex polymerase chain reaction (PCR)-liquid hybridization assay detecting a minimum 10 fg of cytomegaloviral (CMV) DNA has been developed. This assay successfully detected viral nucleic acids in 25/26 (96.2%) routinely embedded allograft liver biopsies with CMV hepatitis. No CMV DNA was detected in 15 native and 12 donor liver tissues sampled at the time of liver transplantation. These results indicate that archived formalin-fixed, paraffin-embedded liver tissues obtained from patients with significant liver disease can be successfully analyzed for CMV by PCR, retrospectively. Failure to detect CMV in native and donor livers implies that any latent virus present within these tissues is very focally distributed, or is below the threshold of detection applicable to PCR.
已开发出一种多重聚合酶链反应(PCR)-液体杂交检测法,可检测至少10 fg的巨细胞病毒(CMV)DNA。该检测法成功在26例常规包埋的伴有CMV肝炎的同种异体移植肝活检组织中的25例(96.2%)中检测到病毒核酸。在肝移植时采集的15例自体肝组织和12例供体肝组织中未检测到CMV DNA。这些结果表明,对于患有严重肝病的患者所获得的存档福尔马林固定、石蜡包埋肝组织,可通过PCR进行回顾性分析,以成功检测CMV。在自体肝和供体肝中未检测到CMV意味着这些组织中存在的任何潜伏病毒分布非常局限,或低于适用于PCR的检测阈值。