Fedorko D P, Ilstrup D M, Smith T F
Section of Clinical Microbiology, Mayo Clinic, Rochester, MN 55905.
Diagn Microbiol Infect Dis. 1990 Jan-Feb;13(1):41-4. doi: 10.1016/0732-8893(90)90052-w.
Pretreatment of MRC-5 cell monolayers in commercially prepared shell vials with 1% dimethyl sulfoxide (DMSO) and 10(-5) mol/L dexamethasone (DEX) was evaluated. Preliminary experiments indicated enhanced infectivity of AD-169 for pretreated MRC-5 cells in shell vials of ages 9 and 16 days. Compared with untreated shell vials, DMSO-DEX increased positivity (day 9, 19 vs. 26 shell vials, p less than 0.03; day 16, 13 vs. 29 shell vials, p less than 0.001) and increased the mean number of fluorescent foci (days 9 and 16, p less than 0.001). Pretreatment of 8-15-day-old monolayers was evaluated clinically using 146 urine specimens. Fifty specimens were positive for cytomegalovirus (CMV) in both treated and untreated shell vials with ten positive in untreated only and three positive in treated only (p = NS). The median number of fluorescent foci was not significantly higher in treated shell vials. Increased toxicity of MRC-5 cells was observed in treated monolayers (p less than 0.0001). Pretreatment with DMSO-DEX did not enhance CMV isolation from clinical specimens and can be toxic to MRC-5 monolayers.
评估了在商业制备的细胞培养瓶中,用1%二甲基亚砜(DMSO)和10⁻⁵mol/L地塞米松(DEX)对MRC-5细胞单层进行预处理的效果。初步实验表明,对于9日龄和16日龄细胞培养瓶中经预处理的MRC-5细胞,AD-169的感染性增强。与未处理的细胞培养瓶相比,DMSO-DEX处理组的阳性率增加(9日龄时,19个 vs. 26个细胞培养瓶,p<0.03;16日龄时,13个 vs. 29个细胞培养瓶,p<0.001),且荧光灶的平均数量增加(9日龄和16日龄时,p<0.001)。使用146份尿液标本对8至15日龄的细胞单层预处理进行了临床评估。在处理和未处理的细胞培养瓶中,50份标本的巨细胞病毒(CMV)检测均为阳性,其中仅未处理组有10份阳性,仅处理组有3份阳性(p=无显著性差异)。处理后的细胞培养瓶中荧光灶的中位数没有显著更高。在处理后的细胞单层中观察到MRC-5细胞毒性增加(p<0.0001)。用DMSO-DEX预处理并不能增强从临床标本中分离CMV,且对MRC-5细胞单层可能有毒性。