Haake David A
Division of Infectious Diseases, 111F, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA 90073; and Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095; Tel.: 310-268-3814; ,
For Immunopathol Dis Therap. 2016;7(3-4):167-174. doi: 10.1615/ForumImmunDisTher.2017020293.
The immune response is a cornerstone in the body's struggle against microbial pathogens. In ways that we do not yet completely understand, the mammalian immune response has evolved to identify proteins of pathogens that are either important virulence factors or key immunoprotective targets. Professor James N. Miller suggested that one way to discover such proteins is to harness the power of the immune system in the laboratory.This general concept, referred to here as the Miller Hypothesis, took several different manifestations in the discovery of some of the best known and widely studied leptospiral proteins: The porin OmpL1 was identified by surface immunoprecipitation, leptospiral immunoglobulin-like proteins were uncovered by screening a genomic library with sera from leptospirosis patients, and the major outer-membrane lipoprotein LipL32 was recognized through immunoblot studies. Such approaches will continue to bear fruit for both the leptospiral research field and research on other invasive pathogens.
免疫反应是机体对抗微生物病原体斗争的基石。以我们尚未完全理解的方式,哺乳动物的免疫反应已经进化到能够识别病原体的蛋白质,这些蛋白质要么是重要的毒力因子,要么是关键的免疫保护靶点。詹姆斯·N·米勒教授提出,发现此类蛋白质的一种方法是在实验室中利用免疫系统的力量。这一总体概念,在此称为米勒假说,在一些最知名且研究广泛的钩端螺旋体蛋白的发现过程中有几种不同的表现形式:孔蛋白OmpL1是通过表面免疫沉淀法鉴定的,钩端螺旋体免疫球蛋白样蛋白是通过用钩端螺旋体病患者的血清筛选基因组文库发现的,主要外膜脂蛋白LipL32是通过免疫印迹研究识别的。此类方法将继续为钩端螺旋体研究领域以及其他侵袭性病原体的研究带来成果。