Appelmelk B J, Verweij-van Vught A M, Brade H, Maaskant J J, Schouten W F, Thijs L G, MacLaren D M
Department of Medical Microbiology, Vrije Universiteit, School of Medicine, Amsterdam, The Netherlands.
Microb Pathog. 1988 Oct;5(4):251-7. doi: 10.1016/0882-4010(88)90097-6.
Murine monoclonal antibodies reacting with lipopolysaccharide (LPS) of Salmonella minnesota strain R595 (Re chemotype) were prepared, and tested for their ability to protect actinomycin D-sensitized mice against lethal endotoxemia. Protection was found with some antibodies up to a 90-fold increase in LD50, whereas others exhibited no protection. The various protective antibodies did not all bind to the same epitope. The same applied for non-protective clones. Protective and non-protective clones could not be discriminated by ELISA. One protective monoclonal antibody (clone 20) was specific for ketodeoxyoctonate, a structural element common to various LPS. These findings show that the involvement of lipid A in the binding site of monoclonal antibodies is no prerequisite for protection.
制备了与明尼苏达沙门氏菌R595菌株(Re化学型)脂多糖(LPS)反应的鼠单克隆抗体,并测试了它们保护放线菌素D致敏小鼠免受致死性内毒素血症的能力。发现一些抗体具有保护作用,使半数致死剂量(LD50)增加了90倍,而其他抗体则没有保护作用。各种保护性抗体并非都结合到相同的表位。非保护性克隆也是如此。通过酶联免疫吸附测定(ELISA)无法区分保护性和非保护性克隆。一种保护性单克隆抗体(克隆20)对酮脱氧辛糖酸具有特异性,酮脱氧辛糖酸是各种LPS共有的结构成分。这些发现表明,脂质A参与单克隆抗体的结合位点并非保护作用的先决条件。