Verdrengh M, Springer T A, Gutierrez-Ramos J C, Tarkowski A
Department of Clinical Immunology, University of Göteborg, Sweden.
Infect Immun. 1996 Jul;64(7):2804-7. doi: 10.1128/iai.64.7.2804-2807.1996.
Intercellular adhesion molecule 1 (ICAM-1) is a member of the immunoglobulin superfamily that interacts with two integrins, LFA-1 and Mac-1. These interactions are critical for leukocyte extravasation into inflamed tissue. To assess the role of ICAM-1 expression in the pathogenesis of bacterial infection, homozygously mutant mice lacking the ICAM-1 gene were exposed to Staphylococcus aureus. Within 6 days after inoculation 50% of the animals in the ICAM-1(-/-) group, but none of the controls, had died. Despite the high level of mortality, ICAM-1(-/-) mice developed less frequent and less severe arthritis than their wild-type littermates. In agreement, normal mice inoculated with staphylococci and administered anti-ICAM-1 antibodies exhibited a higher frequency of mortality but less severe arthritis than the controls. Our results indicate that ICAM-1 on the one hand provides protection against systemic disease but on the other hand aggravates the local disease manifestation.
细胞间黏附分子1(ICAM-1)是免疫球蛋白超家族的成员,它可与两种整合素LFA-1和Mac-1相互作用。这些相互作用对于白细胞渗入炎症组织至关重要。为了评估ICAM-1表达在细菌感染发病机制中的作用,将缺乏ICAM-1基因的纯合突变小鼠暴露于金黄色葡萄球菌。接种后6天内,ICAM-1(-/-)组中有50%的动物死亡,而对照组无一死亡。尽管死亡率很高,但ICAM-1(-/-)小鼠发生关节炎的频率和严重程度均低于其野生型同窝小鼠。同样,接种葡萄球菌并给予抗ICAM-1抗体的正常小鼠死亡率较高,但关节炎严重程度低于对照组。我们的结果表明,ICAM-1一方面提供针对全身性疾病的保护,但另一方面会加重局部疾病表现。