Jiwa N M, Kanavaros P, De Bruin P C, van der Valk P, Horstman A, Vos W, Mullink H, Walboomers J M, Meijer C J
Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.
J Pathol. 1993 Jun;170(2):129-36. doi: 10.1002/path.1711700206.
Forty-four cases of Hodgkin's disease (HD), mostly of the nodular sclerosing type, were investigated for the presence of Epstein-Barr virus (EBV) by polymerase chain reaction (PCR) and DNA and RNA in situ hybridization (DISH, RISH), as well as by immunohistochemistry for the detection of latent membrane protein-1 (LMP-1) of EBV. In situ hybridization (ISH) was combined with immunohistochemistry to correlate the presence and activity of the virus at the cellular level. In 18/34 (53 per cent) cases, EBV-DNA sequences could be detected with the PCR method. In 12/18 positive cases, DISH and RISH were also positive. In the remaining six EBV-PCR positive cases, two were also positive with RISH and LMP-1, whereas no positive signal with DISH could be obtained. All DISH and/or RISH positive cases were also positive for LMP-1. With RISH, not only the Reed-Sternberg cells and their mononuclear variants (RS cells) stained positive, but also small and intermediate cells frequently reacted with the EBV-specific probes (EBER-1 and -2). Double staining with cellular markers (CD3, CD20, CD45, CD45RO, CD68, and the lectin PNA) revealed that most of the smaller EBER-positive cells frequently did not express T, B, or histiocytic markers, but that they, as well as the RS cells, showed cytoplasmic and membranous staining with PNA. These smaller EBER-positive cells were not found in EBV-PCR negative HD. EBER-positive RS cells were almost always LMP-1 positive, as well as a substantial proportion of the intermediate-sized cells, whereas the majority of the small EBER-positive cells remained LMP-1 negative.(ABSTRACT TRUNCATED AT 250 WORDS)
对44例霍奇金淋巴瘤(HD)患者进行了研究,这些患者大多为结节硬化型。采用聚合酶链反应(PCR)、DNA和RNA原位杂交(DISH、RISH)以及免疫组织化学方法检测爱泼斯坦-巴尔病毒(EBV)的潜伏膜蛋白-1(LMP-1),以确定EBV的存在情况。原位杂交(ISH)与免疫组织化学相结合,在细胞水平上关联病毒的存在和活性。在34例患者中的18例(53%),可通过PCR方法检测到EBV-DNA序列。在18例阳性病例中的12例,DISH和RISH也呈阳性。在其余6例EBV-PCR阳性病例中,2例RISH和LMP-1也呈阳性,而DISH未获得阳性信号。所有DISH和/或RISH阳性病例的LMP-1也呈阳性。采用RISH时,不仅里德-施特恩伯格细胞及其单核变体(RS细胞)染色呈阳性,而且小细胞和中等大小细胞也经常与EBV特异性探针(EBER-1和-2)发生反应。用细胞标志物(CD3、CD20、CD45、CD45RO、CD68和凝集素PNA)进行双重染色显示,大多数较小的EBER阳性细胞通常不表达T、B或组织细胞标志物,但它们以及RS细胞用PNA染色时显示胞质和膜染色。在EBV-PCR阴性HD中未发现这些较小的EBER阳性细胞。EBER阳性的RS细胞几乎总是LMP-1阳性,相当一部分中等大小细胞也是如此,而大多数小EBER阳性细胞LMP-1仍为阴性。(摘要截短至250字)