Henry M, Uthman A, Geusau A, Rieger A, Furci L, Lazzarin A, Lusso P, Tschachler E
Division of Immunology, Allergy and Infectious Diseases, Department of Dermatology, Vienna Medical School, Austria.
J Invest Dermatol. 1999 Oct;113(4):613-6. doi: 10.1046/j.1523-1747.1999.00733.x.
Human herpesvirus type 8 (HHV-8) has been identified as the most likely candidate to be involved in the development of Kaposi's Sarcoma (KS). HHV-8 has been associated with all forms of KS, primary effusion lymphoma, and multicentric Castleman's disease and detected in various non-neoplastic cells. Its presence in cells of the different hemopoietic lineages has not yet been investigated in a comprehensive and systematic manner. In this study we searched for the presence of HHV-8 in different subpopulations of peripheral blood mononuclear cells (PBMC) from patients with classic and AIDS-associated KS, as well as from HIV-1 sero-positive and sero-negative persons without KS. Thirty-four samples of PBMC were isolated from 30 patients. Subpopulations were isolated with immunomagnetic beads. Polymerase chain reaction for HHV-8 DNA was performed on PBMC and subpopulations with a primer pair selected from ORF26 of the viral genome. Polymerase chain reaction products were subsequently Southern blotted and hybridized. In patients with KS, HHV-8 DNA was detected in nine of 11 (81%) CD19+ cells, four of 11 (36%) CD2+ cells, three of 11 (27%) CD14+ cells, and nine of 11 (81%) of the remaining depleted cell populations (DP) that contain CD34 positive cells. In a subsequent set of experiments HHV-8 DNA was detected in 10 of 12 (83%) CD34 positive cell fractions. All cell subpopulations from the non-KS group were HHV-8 negative, with the exception of one positive B cell sample obtained from an HIV-infected patient. Our data demonstrate that in peripheral blood HHV-8 is detectable not only in CD19+ cells, as previously reported, but also in other cells, including T cells, monocytes, and cells devoid of specific lineage markers. We also show for the first time that CD34+ cells in peripheral blood of KS patients are a predominant HHV-8-harboring population, suggesting that they represent an additional important reservoir for this virus in vivo.
人类疱疹病毒8型(HHV-8)已被确定为最有可能与卡波西肉瘤(KS)发病相关的病毒。HHV-8与各种形式的KS、原发性渗出性淋巴瘤和多中心Castleman病相关,并在多种非肿瘤细胞中被检测到。其在不同造血谱系细胞中的存在尚未得到全面系统的研究。在本研究中,我们在经典型和艾滋病相关型KS患者以及无KS的HIV-1血清阳性和血清阴性个体的外周血单个核细胞(PBMC)的不同亚群中寻找HHV-8的存在。从30例患者中分离出34份PBMC样本。用免疫磁珠分离亚群。用从病毒基因组的ORF26中选择的引物对,对PBMC及其亚群进行HHV-8 DNA的聚合酶链反应。聚合酶链反应产物随后进行Southern印迹和杂交。在KS患者中,在11个CD19 +细胞中的9个(81%)、11个CD2 +细胞中的4个(36%)、11个CD14 +细胞中的3个(27%)以及11个包含CD34阳性细胞的其余耗尽细胞群体(DP)中的9个(81%)中检测到HHV-8 DNA。在随后的一组实验中,在12个CD34阳性细胞组分中的10个(83%)中检测到HHV-8 DNA。除了从一名HIV感染患者获得的一份阳性B细胞样本外,非KS组的所有细胞亚群均为HHV-8阴性。我们的数据表明,在外周血中,HHV-8不仅如先前报道的那样可在CD19 +细胞中检测到,而且还可在包括T细胞、单核细胞和缺乏特异性谱系标记的细胞在内的其他细胞中检测到。我们还首次表明,KS患者外周血中的CD34 +细胞是携带HHV-8的主要细胞群体,这表明它们在体内代表了该病毒的另一个重要储存库。