Karray S, DeFrance T, Merle-Béral H, Banchereau J, Debré P, Galanaud P
Institut National de la Recherche Scientifique, Unité 131, Clamart, France.
J Exp Med. 1988 Jul 1;168(1):85-94. doi: 10.1084/jem.168.1.85.
B cells from patients suffering from B-type chronic lymphocytic leukemia (B-CLL) are susceptible to the effects of several interleukins. Using the cells from 12 different patients we show that IL-4 does not synergize with anti-mu antibody for the enhancement of DNA synthesis. Moreover IL-4 profoundly (90%) suppresses the response to IL-2 in the 10 patient responders to this interleukin. This suppression occurs whether IL-2 is used alone, in costimulation with anti-mu antibody, or in synergy with IFN-gamma. In no instance did IL-4 induce terminal differentiation. This negative effect of IL-4 can take place in monoclonal B-CLL cells where IL-4 enhances the expression of CD23. IL-4 does not interfere with the upregulation of CD25 by IL-2. Thus, IL-4 may display inhibitory effects on the proliferative response of selected B cell populations. The antagonism between IL-4 and IL-2 has important implications for the potential use of cytokines in the management of B-CLL patients.
患有B型慢性淋巴细胞白血病(B-CLL)的患者的B细胞对多种白细胞介素的作用敏感。我们使用来自12名不同患者的细胞表明,IL-4不能与抗μ抗体协同作用来增强DNA合成。此外,在10名对这种白细胞介素产生反应的患者中,IL-4显著(90%)抑制了对IL-2的反应。无论IL-2单独使用、与抗μ抗体共刺激还是与IFN-γ协同使用,这种抑制都会发生。IL-4在任何情况下都不会诱导终末分化。IL-4的这种负面影响可发生在单克隆B-CLL细胞中,其中IL-4可增强CD23的表达。IL-4不会干扰IL-2对CD25的上调。因此,IL-4可能对选定的B细胞群体的增殖反应具有抑制作用。IL-4和IL-2之间的拮抗作用对细胞因子在B-CLL患者管理中的潜在应用具有重要意义。