Han X, Itoh K, Balch C M, Pellis N R
Capital Institute of Medicine, Beijing, China.
Lymphokine Res. 1988 Fall;7(3):227-35.
Recombinant interleukin 4 (rIL4) inhibited the proliferation and induction of lymphokine activated killer (LAK) cells in human peripheral blood mononuclear cells (PBMC) cultured in recombinant interleukin 2 (rIL2). Other recombinant cytokines, such as rIFN gamma, rTNF alpha, rIL1, and rIL3, did not inhibit LAK cell induction. rIL4-mediated suppression was dose dependent. As little as 1 U/ml of rIL4 significantly decreased both LAK activity and proliferation of cells induced by incubation of PBMC with 200 U/ml rIL2. Suppression was specific for the induction phase of LAK activity, because rIL4 did not suppress the cytotoxic capability of previously activated LAK cells. rIL4 directly suppressed rIL2-induced activation of precursors into LAK cells, since it inhibited both rIL2-induced proliferation and LAK cell activity in LGL-enriched cell fractions or in purified CD16+ NK cells. Suppressive effects of rIL4 were overcome by adding rIFN gamma to the culture. These results suggest that rIL4 is a potent inhibitor of rIL2-induced activation of PBL, and that the net LAK response in the host may be a function of the production of IL-2, IL-4 and rIFN gamma.
重组白细胞介素4(rIL4)可抑制在重组白细胞介素2(rIL2)中培养的人外周血单个核细胞(PBMC)中淋巴因子激活的杀伤细胞(LAK)的增殖和诱导。其他重组细胞因子,如rIFNγ、rTNFα、rIL1和rIL3,并不抑制LAK细胞的诱导。rIL4介导的抑制作用呈剂量依赖性。低至1 U/ml的rIL4就能显著降低PBMC与200 U/ml rIL2孵育诱导的细胞的LAK活性和增殖。这种抑制作用对LAK活性的诱导阶段具有特异性,因为rIL4并不抑制先前激活的LAK细胞的细胞毒性能力。rIL4直接抑制rIL2诱导的前体细胞向LAK细胞的激活,因为它能抑制富含大颗粒淋巴细胞(LGL)的细胞组分或纯化的CD16 + 自然杀伤细胞(NK细胞)中rIL2诱导的增殖和LAK细胞活性。向培养物中添加rIFNγ可克服rIL4的抑制作用。这些结果表明,rIL4是rIL2诱导的外周血淋巴细胞(PBL)激活的有效抑制剂,并且宿主中的LAK净反应可能是IL-2、IL-4和rIFNγ产生的函数。