Bellos F, Goldschmidt H, Dörner M, Ho A D, Moos M
Department of Internal Medicine V, University of Heidelberg, Germany.
Ann Oncol. 1999 Mar;10(3):323-7. doi: 10.1023/a:1008320717531.
An association between Kaposi's sarcoma associated herpesvirus (KSHV) and the pathogenesis of multiple myeloma (MM) was postulated recently. The dendritic cells of patients with MM were proposed to be infected with the virus.
Bone marrow mononuclear cells (MNC) of 23 patients, 22 with MM and one with MGUS, were cultured according to three distinct protocols for the generation of dendritic cells. One was essentially the stromal cell culture protocol described by Rettig et al. (Science 1997; 276: 1851-4), while the two other protocols comprised growth factors. Cultured cells were characterised by FACS analysis and assessed for the presence of KSHV DNA with a highly sensitive and specific nested PCR assay detecting the KS 330233 sequence of the virus genome followed by hybridisation with a KSHV specific oligonucleotide.
FACS analysis of the cells with the specific markers CD1a, CD86 and HLA-DR, characteristic for dendritic cells, revealed differences in the expression pattern depending on the protocol used. The proportion of CD1a+ cells was very low in the stromal cell cultures (median 0.4%), while a higher percentage of CD14+ cells could be observed (median 37.8%). Growth factor containing cultures revealed a distinctly higher median percentage of CD1a+ cells of 32.5%. The proportion of CD86+ cells varied between 10.4% and 78.5% and HLA-DR+ cells between 26% and 94.4%. Examination of those cells with PCR did not reveal positivity for KSHV in any of the 34 samples assessed. Amplification of seven samples revealed PCR products of approximately the size of the KS 330(233), which, however, could not be confirmed as KSHV specific after hybridisation.
We have no evidence that bone marrow derived dendritic cells from patients with MM are infected with KSHV.
最近有人提出卡波西肉瘤相关疱疹病毒(KSHV)与多发性骨髓瘤(MM)的发病机制之间存在关联。有人认为MM患者的树突状细胞会被该病毒感染。
对23例患者的骨髓单个核细胞(MNC)进行培养以生成树突状细胞,其中22例为MM患者,1例为意义未明的单克隆丙种球蛋白病(MGUS)患者。培养按照三种不同方案进行。一种方案本质上是Rettig等人(《科学》,1997年;276:1851 - 4)描述的基质细胞培养方案,而另外两种方案包含生长因子。通过流式细胞术(FACS)分析对培养的细胞进行表征,并用一种高度敏感且特异的巢式聚合酶链反应(PCR)检测法评估KSHV DNA的存在,该检测法先检测病毒基因组的KS 330233序列,然后与KSHV特异性寡核苷酸杂交。
对具有树突状细胞特征性的特异性标志物CD1a、CD86和HLA - DR的细胞进行FACS分析,结果显示表达模式因所用方案而异。在基质细胞培养中,CD1a +细胞的比例非常低(中位数为0.4%),而可观察到较高比例的CD14 +细胞(中位数为37.8%)。含生长因子的培养物显示CD1a +细胞的中位数百分比明显更高达32.5%。CD86 +细胞的比例在10.4%至78.5%之间,HLA - DR +细胞的比例在26%至94.4%之间。用PCR检测这些细胞,在评估的34个样本中均未发现KSHV呈阳性。7个样本的扩增显示出大小约为KS 330(233)的PCR产物,然而,杂交后不能确认为KSHV特异性。
我们没有证据表明MM患者骨髓来源的树突状细胞被KSHV感染。