Childers N K, Denys F R, McGee N F, Michalek S M
Department of Community and Public Health Dentistry, School of Dentistry University of Alabama, Birmihgam 35294.
Reg Immunol. 1990 Jan-Feb;3(1):8-16.
Liposomes (phospholipid artificial membrane vesicles) have been used in targeted drug delivery and recently in the development of oral vaccines using purified soluble antigens for the induction of mucosal immune responses. Although the mechanisms by which liposomes promote the induction of responses to soluble antigens have not been clearly shown, it has been suggested that these vesicles, when given orally, are taken up by M cells for delivery of antigen to underlying lymphoid cells of the Peyer's patch. This study investigated in vivo the uptake of liposomes by cells of Peyer's patch. Following exposure of surgically constricted segments of rat small intestine to small unilamellar liposomes or gold-labelled solid core liposomes, Peyer's patches were removed, fixed, and processed for examination by transmission electron microscopy. Sections of Peyer's patch from experimental animals showed M cells with endocytic vesicles containing liposomes. Vesicles containing liposomes were also observed between M cells and lymphoid cells. These results indicate that intact liposomes are endocytosed by M cells and provide evidence for a possible mechanism by which M cells deliver antigen to lymphoid cells in the Peyer's patch. These findings support the potential usefulness of liposomes in oral vaccine development.
脂质体(磷脂人工膜囊泡)已被用于靶向给药,最近还被用于开发口服疫苗,该疫苗使用纯化的可溶性抗原来诱导黏膜免疫反应。尽管脂质体促进对可溶性抗原诱导反应的机制尚未明确,但有人提出,这些囊泡口服给药时会被M细胞摄取,从而将抗原递送至派尔集合淋巴结的下层淋巴细胞。本研究在体内研究了派尔集合淋巴结细胞对脂质体的摄取情况。将大鼠小肠手术缩窄段暴露于小单层脂质体或金标记的实心核脂质体后,取出派尔集合淋巴结,固定并进行处理,以便通过透射电子显微镜检查。实验动物的派尔集合淋巴结切片显示,M细胞含有包含脂质体的内吞囊泡。在M细胞和淋巴细胞之间也观察到了含有脂质体的囊泡。这些结果表明,完整的脂质体被M细胞内吞,并为M细胞将抗原递送至派尔集合淋巴结中的淋巴细胞的可能机制提供了证据。这些发现支持了脂质体在口服疫苗开发中的潜在用途。