Dunn D L
Pharmacotherapy. 1987;7(2):S31-5. doi: 10.1002/j.1875-9114.1987.tb03511.x.
Gram-negative bacterial sepsis continues to represent a significant cause of morbidity and mortality in hospitalized patients. Currently available medical therapy (antimicrobial agents, hemodynamic monitoring, aggressive fluid resuscitation, and nutritional support) for this disease process has reduced but not eliminated the severe consequences that may ensue. Recent investigations have demonstrated the ability of antibody directed against gram-negative bacterial lipopolysaccharide (LPS or endotoxin) to afford protection during experimental gram-negative bacillary sepsis. The core LPS-lipid A portion of endotoxin represents a determinant shared by many common gram-negative microorganisms that is luxuriantly expressed on the cell surface of rough mutants of Escherichia coli and Salmonella minnesota. These organisms or the outer membrane LPS isolated from them thus represent suitable immunogens for the development of cross-protective antibody preparations. Large quantities of highly cross-reactive antibody may potentially be obtained from several sources: murine or human monoclonal antibodies, immunization of large animals or humans with subsequent plasmapharesis and antibody isolation, affinity purification of large amounts of normal antibody, and pooling of prescreened lots of normal animal or human antibody that react to a particular bacterial antigen.
革兰氏阴性菌败血症仍然是住院患者发病和死亡的一个重要原因。目前针对这一疾病过程的医学治疗方法(抗菌药物、血流动力学监测、积极的液体复苏和营养支持)虽已降低但并未消除可能随之而来的严重后果。最近的研究表明,针对革兰氏阴性菌脂多糖(LPS或内毒素)的抗体在实验性革兰氏阴性杆菌败血症期间具有保护作用。内毒素的核心LPS-脂质A部分是许多常见革兰氏阴性微生物共有的决定簇,在大肠杆菌和明尼苏达沙门氏菌粗糙突变体的细胞表面大量表达。因此,这些生物体或从它们中分离出的外膜LPS代表了开发交叉保护性抗体制剂的合适免疫原。大量高度交叉反应性抗体可能从几个来源获得:鼠源或人源单克隆抗体、用后续血浆置换和抗体分离法对大型动物或人进行免疫、大量正常抗体的亲和纯化,以及汇集预先筛选的对特定细菌抗原产生反应的正常动物或人抗体批次。