Conlan J W, North R J
Trudeau Institute, Inc., Saranac Lake, NY 12983.
J Leukoc Biol. 1992 Jul;52(1):130-2. doi: 10.1002/jlb.52.1.130.
Treatment of mice with a monoclonal antibody (mAb) designated NIMP-R10, directed against the CD11b polypeptide of the CD18/CD11b heterodimeric type 3 complement receptor (CR3), exacerbates listeriosis by preventing myelomonocytic cells from focusing at sites of infected hepatocytes in the liver. Under these conditions an otherwise sublethal Listeria inoculum grows unrestrictedly within hepatocytes and causes death in 3 days. The results obtained with NIMP-R10 are similar to those previously obtained with a different anti-CD11b mAb (5C6), although mAb NIMP-R10 is more effective at enhancing infection. Therefore, both mAbs can be used to analyze host antibacterial defenses in vivo.
用一种名为NIMP-R10的单克隆抗体(mAb)治疗小鼠,该抗体针对CD18/CD11b异二聚体型3补体受体(CR3)的CD11b多肽,通过阻止骨髓单核细胞聚集在肝脏中受感染的肝细胞部位,加重了李斯特菌病。在这些条件下,原本亚致死剂量的李斯特菌接种物在肝细胞内不受限制地生长,并在3天内导致死亡。用NIMP-R10获得的结果与先前用另一种抗CD11b mAb(5C6)获得的结果相似,尽管mAb NIMP-R10在增强感染方面更有效。因此,这两种mAb均可用于体内分析宿主的抗菌防御。