Zarember Kol A, Malech Harry L
Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
J Clin Invest. 2005 Jul;115(7):1702-4. doi: 10.1172/JCI25740.
In the days following infection, when the human body develops and refines antibodies and prepares to mount an adaptive immune response, the bulwark of innate host defense against microbial infection is the polymorphonuclear leukocyte (PMN). PMNs seek out, identify, engulf, and sterilize invading microbes using both O2-dependent and O2-independent antimicrobial systems. A decrease in PMN numbers or function caused by immunosuppression or disease increases the risk of infection. In this issue of the JCI, Peyssonnaux et al. identify a novel and essential role for hypoxia-inducible factor-1alpha in regulating several important PMN functions relevant to host defense, including transcription of cationic antimicrobial polypeptides and induction of NO synthase.
在感染后的数天里,当人体产生并完善抗体,准备发起适应性免疫反应时,抵御微生物感染的固有宿主防御的堡垒是多形核白细胞(PMN)。PMN利用依赖氧气和不依赖氧气的抗菌系统寻找、识别、吞噬并杀灭入侵的微生物。免疫抑制或疾病导致的PMN数量减少或功能下降会增加感染风险。在本期《临床研究杂志》中,佩松诺等人发现缺氧诱导因子-1α在调节与宿主防御相关的几种重要PMN功能中具有新的关键作用,包括阳离子抗菌多肽的转录和一氧化氮合酶的诱导。