Belosevic M, Davis C E, Meltzer M S, Nacy C A
Department of Immunology, Walter Reed Army Institute of Research, Washington, DC 20307.
J Immunol. 1988 Aug 1;141(3):890-6.
Macrophages exposed to lymphokines (LK) before exposure to parasites develop the capacity to resist infection with amastigotes of Leishmania major. Activity of LK for induction of this activated macrophage effector function is abrogated by depleting the LK of IFN-gamma, yet IFN-gamma is incapable of inducing the activity by itself. To identify the factors in LK that serve as second signals for induction of resistance to infection, we exposed macrophages to the following cytokines available as recombinant or highly purified reagents: CSF-1, granulocyte/macrophage colony-stimulating factor (GM-CSF), IL-1, -2, -3, -4, and -5, and IFN-alpha/beta. None of these factors induced resistance to infection by themselves or in combination with each other; in the presence of 50 U/ml IFN-gamma, three cytokines were active: GM-CSF, IL-2, and IL-4. IFN-gamma was an essential component of the activation cascade but was insufficient by itself to induce the effector reaction. Cytokines that act as cofactors with IFN-gamma worked directly on macrophages and not through another cell in the peritoneal cell (PC) cultures. Activation of PC depleted of Thy-1.2+ cells (85 +/- 5% macrophages) and bone marrow-derived macrophages (100% macrophages) showed that 50% maximal doses of GM-CSF, IL-2, and IL-4 for these macrophage-enriched populations were not different than for untreated PC. Unlike other effector reactions of activated macrophages, bacterial LPS did not synergistically enhance the activity of any of the cytokines, alone or in combination with IFN-gamma. Antibody depletion of the active cytokines from LK, singly or in combination, failed to alter the dose response of the active factors in whole LK for induction of resistance to infection. Thus, multiple factors can provide the second signal for IFN-gamma in the induction of resistance to infection, namely, GM-CSF, IL-2, IL-4, and at least two additional undefined factors in whole LK. Resistance to infection may be the first example of an activated macrophage effector reaction that has an absolute requirement for more than one endogenous signal for its induction.
在接触寄生虫之前先接触淋巴因子(LK)的巨噬细胞会产生抵抗硕大利什曼原虫无鞭毛体感染的能力。通过去除LK中的γ干扰素(IFN-γ),可消除LK诱导这种活化巨噬细胞效应功能的活性,但IFN-γ自身无法诱导该活性。为了确定LK中作为诱导抗感染能力第二信号的因子,我们将巨噬细胞暴露于以下可作为重组或高度纯化试剂获得的细胞因子:集落刺激因子-1(CSF-1)、粒细胞/巨噬细胞集落刺激因子(GM-CSF)、白细胞介素-1、-2、-3、-4和-5,以及α/β干扰素。这些因子单独或相互组合均不能诱导抗感染能力;在存在50 U/ml IFN-γ的情况下,三种细胞因子具有活性:GM-CSF、白细胞介素-2和白细胞介素-4。IFN-γ是激活级联反应的必需成分,但自身不足以诱导效应反应。与IFN-γ起辅助因子作用的细胞因子直接作用于巨噬细胞,而不是通过腹腔细胞(PC)培养中的另一种细胞。对去除Thy-1.2+细胞(85±5%为巨噬细胞)的PC和骨髓来源的巨噬细胞(100%为巨噬细胞)进行激活,结果表明,对于这些富含巨噬细胞的群体,GM-CSF、白细胞介素-2和白细胞介素-4的50%最大剂量与未处理的PC并无差异。与活化巨噬细胞的其他效应反应不同,细菌脂多糖单独或与IFN-γ联合使用时,均不会协同增强任何一种细胞因子的活性。从LK中单独或联合去除活性细胞因子的抗体,不会改变整个LK中活性因子诱导抗感染能力的剂量反应。因此,多种因子可在诱导抗感染能力时为IFN-γ提供第二信号,即GM-CSF、白细胞介素-2和白细胞介素-4,以及整个LK中至少另外两种未明确的因子。抗感染能力可能是活化巨噬细胞效应反应的首个例子,即其诱导绝对需要不止一种内源性信号。