首页> 美国卫生研究院文献>British Journal of Experimental Pathology >Inhibition of the presentation of dengue virus antigen by macrophages to B cells by serine-protease inhibitors.
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Inhibition of the presentation of dengue virus antigen by macrophages to B cells by serine-protease inhibitors.

机译:丝氨酸蛋白酶抑制剂抑制巨噬细胞向B细胞呈递登革热病毒抗原。

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摘要

It has been shown that macrophages (M phi) process dengue type 2 virus (DV) antigen and present it to B cells leading to their clonal expansion as shown by DV-specific IgM antibody plaque-forming cell (PFC) count in spleen. The present study was undertaken to find out the nature of enzymes responsible for the processing of DV antigen in M phi. DV-pulsed M phi were treated with seven different protease inhibitors and then assayed for antigen presentation to B cells. It was observed that maximum inhibition occurred by treatment of M phi with PMSF, a serine-protease inhibitor. The effect of PMSF was dose dependent and was abolished by using predigested antigen. PMSF inhibited presentation of DV and sheep RBC antigens but had no effect on presentation of bovine serum albumin which does not require processing. The results thus identify the serine group of proteases as the main enzymes involved in processing the DV antigen in M phi.
机译:已显示巨噬细胞(M phi)处理登革2型病毒(DV)抗原并将其呈递给B细胞,导致其克隆扩增,如脾脏中DV特异性IgM抗体斑块形成细胞(PFC)所示。进行本研究以发现负责处理M phi中DV抗原的酶的性质。用七种不同的蛋白酶抑制剂处理DV脉冲的M phi,然后测定向B细胞的抗原呈递。观察到最大抑制作用是通过用丝氨酸蛋白酶抑制剂PMSF处理M phi而发生的。 PMSF的作用是剂量依赖性的,并且通过使用预先消化的抗原可以消除。 PMSF抑制了DV和绵羊RBC抗原的呈递,但对不需要加工的牛血清白蛋白的呈递没有影响。因此,结果确定了蛋白酶的丝氨酸基团是参与在M phi中加工DV抗原的主要酶。

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