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含脂质A的脂质体的佐剂效应:增强脂质体抗原呈递及巨噬细胞募集。

Adjuvant effects of liposomes containing lipid A: enhancement of liposomal antigen presentation and recruitment of macrophages.

作者信息

Verma J N, Rao M, Amselem S, Krzych U, Alving C R, Green S J, Wassef N M

机构信息

Department of Membrane Biochemistry, Walter Reed Army Institute of Research, Washington, D.C. 20307-5100.

出版信息

Infect Immun. 1992 Jun;60(6):2438-44. doi: 10.1128/iai.60.6.2438-2444.1992.

DOI:10.1128/iai.60.6.2438-2444.1992
PMID:1587611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC257178/
Abstract

Liposomes containing lipid A induced potent humoral immune responses in mice against an encapsulated malaria antigen (R32NS1) containing NANP epitopes. The immune response was not enhanced by lipid A alone or by empty liposomes containing lipid A. Experiments to investigate the adjuvant mechanisms of liposomes and lipid A revealed that liposome-encapsulated R32NS1 was actively presented by bone marrow-derived macrophages to NANP-specific cloned T cells. The degree of presentation was related to the amount of liposomal antigen added per macrophage in the culture medium. At high cell densities, poor presentation occurred when liposomes lacked lipid A but excellent presentation occurred when the liposomes contained lipid A. Liposomes containing lipid A and encapsulated antigen also activated gamma interferon-treated macrophages to produce nitric oxide. Macrophage activation and antigen presentation occurred with liposomes that could not be detected by the Limulus amebocyte lysis assay. Intraperitoneal injection of liposomal lipid A caused a marked increase in the recruitment of immature (peroxidase-positive) macrophages to the peritoneum. On the basis of these experiments, we propose that the mechanism of the adjuvant action of liposomal lipid A is partly due to increased antigen presentation by macrophages and partly due to recruitment of an increased number of macrophages serving as antigen-presenting cells.

摘要

含有脂多糖A的脂质体在小鼠体内诱导了针对含NANP表位的包囊型疟疾抗原(R32NS1)的强烈体液免疫反应。单独的脂多糖A或含有脂多糖A的空脂质体均未增强免疫反应。研究脂质体和脂多糖A佐剂机制的实验表明,脂质体包裹的R32NS1由骨髓来源的巨噬细胞呈递给NANP特异性克隆T细胞。呈递程度与培养基中每个巨噬细胞添加的脂质体抗原量有关。在高细胞密度下,当脂质体缺乏脂多糖A时呈递较差,但当脂质体含有脂多糖A时呈递良好。含有脂多糖A和包裹抗原的脂质体还激活经γ干扰素处理的巨噬细胞产生一氧化氮。巨噬细胞激活和抗原呈递发生在鲎试剂检测无法检测到的脂质体中。腹腔注射脂质体脂多糖A导致未成熟(过氧化物酶阳性)巨噬细胞向腹膜的募集显著增加。基于这些实验,我们提出脂质体脂多糖A的佐剂作用机制部分归因于巨噬细胞抗原呈递增加,部分归因于作为抗原呈递细胞的巨噬细胞数量增加。

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