Mukerjee R, Chaturvedi U C, Dhawan R
Postgraduate Department of Microbiology, K. G. Medical College, Lucknow, India.
Clin Exp Immunol. 1995 Nov;102(2):262-7. doi: 10.1111/j.1365-2249.1995.tb03775.x.
During dengue type 2 virus (DV) infection of mice a unique cytokine, the cytotoxic factor (CF), is produced which reproduces the pathological lesions seen in patients of dengue haemorrhagic fever (DHF). Recently we have observed a CF-like protein in the sera of DHF cases. The present study was undertaken to investigate whether DV can stimulate human peripheral blood mononuclear cells (PBMC) in vitro to produce human CF (hCF). Cultures prepared from PBMC or its enriched subpopulations were inoculated with 1000 LD50 of DV and controls with normal mouse brain suspension (NMB). Aliquots of cultures were harvested daily from 24 h to 96 h and their supernatant (CS) and cells were separated. CS were screened for viral titres and for the presence of hCF by cytotoxicity assay, inhibition ELISA, dot blot and Western blot tests using anti-mouse-CF antibodies. The RNA from the cells was screened in Northern blot and dot blot tests for the presence of mRNA for CF. It was observed that hCF appeared in the CS of DV-infected culture of PBMC and T-enriched cells at 48 h and was present until 96 h; no CF was detected in CS of B cells or monocyte cultures. The production of hCF was abrogated by pretreatment of the T cells with anti-CD4 antibodies but not with anti-CD8 antibodies, indicating that hCF was produced by CD4+ T cells. The Northern blot analysis using oligonucleotide probes prepared on the basis of amino-terminal sequence of mouse CF, showed presence of mRNA for hCF in PBMC and T cell cultures. DV replicated in PBMC cultures with peak titres at 48 h. The findings of the present study demonstrate that DV-induced hCF is produced by human T cells.
在小鼠感染2型登革病毒(DV)期间,会产生一种独特的细胞因子——细胞毒性因子(CF),它会重现登革出血热(DHF)患者身上出现的病理损伤。最近我们在DHF病例的血清中观察到一种类似CF的蛋白质。本研究旨在调查DV是否能在体外刺激人外周血单核细胞(PBMC)产生人CF(hCF)。用1000 LD50的DV接种由PBMC或其富集亚群制备的培养物,并以正常小鼠脑悬液(NMB)作为对照。从24小时到96小时每天收集培养物的等分试样,并分离其上清液(CS)和细胞。通过细胞毒性试验、抑制ELISA、斑点印迹和使用抗小鼠CF抗体的蛋白质印迹试验,对CS进行病毒滴度和hCF存在情况的筛查。通过Northern印迹和斑点印迹试验对细胞的RNA进行CF mRNA存在情况的筛查。观察到hCF在PBMC和富含T细胞的培养物被DV感染后的CS中于48小时出现,并持续存在至96小时;在B细胞或单核细胞培养物的CS中未检测到CF。用抗CD4抗体预处理T细胞可消除hCF的产生,但用抗CD8抗体则不能,这表明hCF是由CD4 + T细胞产生的。使用基于小鼠CF氨基末端序列制备的寡核苷酸探针进行的Northern印迹分析表明,PBMC和T细胞培养物中存在hCF的mRNA。DV在PBMC培养物中复制,在48小时达到滴度峰值。本研究结果表明,DV诱导产生的hCF是由人T细胞产生的。