Loo L S, Tang J P, Kohl S
J Infect Dis. 1982 Jul;146(1):64-70. doi: 10.1093/infdis/146.1.64.
The effect of intralipid, a lipid emulsion used in total parenteral nutrition, on cellular cytotoxicity for herpes simplex virus (HSV)-infected cells was analyzed. In vitro, intralipid inhibited antibody-dependent cellular cytotoxicity (ADCC) of lymphocytes, monocytes-macrophages, and polymorphonuclear leukocytes and natural killer cytotoxicity of lymphocytes for radiolabeled HSV-infected liver cells. This was due to an effect on the leukocytes, rather than on the target cells. Intralipid did not affect leukocyte viability but inhibited the expression of leukocyte Fc receptors necessary for cytotoxicity. In vivo, intralipid inhibited murine ADCC and completely nullified the protection against lethal infection with HSV in neonatal mice afforded by the administration of human leukocytes and antibody. These data suggest that high levels of circulating intralipid may interfere with antiviral immunity in humans and predispose hosts who are already compromised to severe viral infections.
分析了全胃肠外营养中使用的脂肪乳剂英脱利匹特对单纯疱疹病毒(HSV)感染细胞的细胞毒性作用。在体外,英脱利匹特抑制淋巴细胞、单核巨噬细胞和多形核白细胞的抗体依赖性细胞毒性(ADCC)以及淋巴细胞对放射性标记的HSV感染肝细胞的自然杀伤细胞毒性。这是由于对白细胞的作用,而非对靶细胞的作用。英脱利匹特不影响白细胞活力,但抑制细胞毒性所需的白细胞Fc受体的表达。在体内,英脱利匹特抑制小鼠ADCC,并完全消除了给予人白细胞和抗体对新生小鼠HSV致死性感染的保护作用。这些数据表明,高水平循环的英脱利匹特可能干扰人体的抗病毒免疫,并使已处于免疫受损状态的宿主易患严重病毒感染。