Flescher E, Bowlin T L, Ballester A, Houk R, Talal N
Clinical Immunology Section, Audie L. Murphy Memorial Veterans Hospital, San Antonio, Texas.
J Clin Invest. 1989 Apr;83(4):1356-62. doi: 10.1172/JCI114023.
Polyamines downregulate immune reactivity. RA is associated with decreased IL 2 production. In this study, we present evidence to suggest that excessive polyamines can contribute to the IL 2 deficiency in RA. Blocking polyamine production with inhibitors of ornithine decarboxylase results in increased IL 2 production by RA PBMC. Moreover, polyamine oxidase (PAO) inhibitors and catalase also increase IL 2 production by RA PBMC. This effect of PAO inhibition is monocyte mediated. After 3 d in culture, RA PBMC produce three times more IL 2 than do normal PBMC. This rise is prevented by exogenous spermidine but only in the presence of monocytes. The concentration of polyamines in RA PBMC and synovial fluid MNC is 2-20-fold higher than in normal cells. Thus, polyamines and their oxidation products downregulate IL 2 production by RA PBMC and may account for the decreased T cell effector function seen in this disease.
多胺可下调免疫反应性。类风湿关节炎(RA)与白细胞介素2(IL - 2)产生减少有关。在本研究中,我们提供证据表明,过多的多胺可能导致RA患者IL - 2缺乏。用鸟氨酸脱羧酶抑制剂阻断多胺生成会使RA患者外周血单个核细胞(PBMC)的IL - 2产生增加。此外,多胺氧化酶(PAO)抑制剂和过氧化氢酶也会增加RA患者PBMC的IL - 2产生。PAO抑制的这种作用是由单核细胞介导的。培养3天后,RA患者PBMC产生的IL - 2比正常PBMC多两倍。外源性亚精胺可阻止这种升高,但仅在有单核细胞存在时有效。RA患者PBMC和滑膜液单个核细胞(MNC)中的多胺浓度比正常细胞高2至20倍。因此,多胺及其氧化产物下调RA患者PBMC的IL - 2产生,这可能是该疾病中T细胞效应功能降低的原因。