Newton R C
Immunology. 1985 Nov;56(3):441-9.
This study investigates the effect of interferons on the induction of human monocyte secretion of interleukin-1 (IL-1) activity by lipopolysaccharides (LPS). Monocytes do not spontaneously produce IL-1 and the addition of interferons to the culture does not lead to detectable secretion. Addition of LPS alone induces the release of measurable amounts of IL-1 activity. The addition of low doses (1-10 units/ml) of alpha, beta, or gamma interferon to the LPS-stimulated cultures further increases this secretion by 50%. The addition of 1000 units/ml of alpha or beta interferon leads to inhibition of IL-1 release. By contrast, gamma interferon is a dose dependent enhancer of IL-1 release. The effect of gamma interferon is on the production of IL-1 and is not an enhancement of IL-1 activity in the biological assay. Results demonstrate that addition of gamma interferon to monocytes increases the rate of secretion of IL-1 by these cells. Gamma interferon also appears to abrogate the loss in the ability of monocytes to produce IL-1 activity after overnight culture. This last result parallels the maintainence of the expression of the HLA-DR surface marker on monocytes by gamma interferon. These results may help define a mechanism involving IL-1 generation which could have bearing on the in vivo pyrogenic effects of purified gamma interferon.
本研究调查了干扰素对脂多糖(LPS)诱导人单核细胞分泌白细胞介素-1(IL-1)活性的影响。单核细胞不会自发产生IL-1,且在培养物中添加干扰素不会导致可检测到的分泌。单独添加LPS可诱导释放可测量量的IL-1活性。向LPS刺激的培养物中添加低剂量(1 - 10单位/毫升)的α、β或γ干扰素可使这种分泌进一步增加50%。添加1000单位/毫升的α或β干扰素会导致IL-1释放受到抑制。相比之下,γ干扰素是IL-1释放的剂量依赖性增强剂。γ干扰素的作用在于IL-1的产生,而非在生物学检测中增强IL-1活性。结果表明,向单核细胞中添加γ干扰素可增加这些细胞分泌IL-1的速率。γ干扰素似乎还能消除单核细胞在过夜培养后产生IL-1活性的能力损失。这一最终结果与γ干扰素维持单核细胞表面HLA - DR标记物表达的情况相似。这些结果可能有助于确定一种涉及IL-1产生的机制,这可能与纯化的γ干扰素在体内的致热作用有关。