Goldman M
Bull Mem Acad R Med Belg. 2000;155(1-2):141-5; discussion 145-6.
Interleukin-5 produced by Th2-type lymphocytes is involved in the pathogenesis of several hypereosinophilic disorders. We have identified clonal Th2 cells in the peripheral blood of three patients with the idiopathic hypereosinophilic syndrome. Costimulatory signaling through B7/CD28 and LFA-3/CD2 pathways cooperates with an autocrine interleukin-2/interleukin-2 receptor loop for the survival and proliferation of these Th2 cells, as well as their production of cytokines, independently of T cell receptor engagement. The high-level of spontaneous apoptosis displayed by these cells was inhibited by interleukin-2 and interferon-g. New therapeutic strategies could result from our observations. Indeed, the hypereosinophilic syndrome may represent an unexpected indication for new immunomodulatory molecules such as CTLA4-Ig and anti-il-2 receptor antibodies.
Th2型淋巴细胞产生的白细胞介素-5参与多种嗜酸性粒细胞增多性疾病的发病机制。我们在3例特发性嗜酸性粒细胞增多综合征患者的外周血中鉴定出克隆性Th2细胞。通过B7/CD28和LFA-3/CD2途径的共刺激信号与自分泌白细胞介素-2/白细胞介素-2受体环协同作用,促进这些Th2细胞的存活和增殖以及它们的细胞因子产生,这一过程独立于T细胞受体的参与。这些细胞表现出的高水平自发凋亡受到白细胞介素-2和干扰素-γ的抑制。我们的观察结果可能会带来新的治疗策略。事实上,嗜酸性粒细胞增多综合征可能是新型免疫调节分子如CTLA4-Ig和抗白细胞介素-2受体抗体意想不到的适应证。