Razi-Wolf Z, Höllander G A, Reiser H
Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2903-8. doi: 10.1073/pnas.93.7.2903.
Interleukin 2 (IL-2)-deficient (IL-2-/-) mice develop hemolytic anemia and chronic inflammatory bowel disease. Importantly, the induction of disease in IL-2-deficient mice is critically dependent on CD4+ T cells. We have studied the requirements of T cells from IL-2-deficient mice for costimulation with B7 antigens. Stable B7-1 or B7-2 chinese hamster ovary (CHO) cell transfectants could synergize with anti-CD3 monoclonal antibody (mAb) to induce the proliferation of CD4+ T cells from IL-2-/- mutant mice. Further mechanistic studies established that B7-induced activation resulted in surface expression of the alpha chain of the IL-2 receptor. B7-induced proliferation occurred independently of IL-4 and was largely independent of the common gamma chain of the IL-2, IL-4, IL-7, IL-9, and IL-15 receptors. Finally, anti-B7-2 but not anti-B7-1 mAb was able to inhibit the activation of IL-2-/- T cells induced by anti-CD3 mAb in the presence of syngeneic antigen-presenting cells. The results of our experiments indicate that IL-2-/- CD4+ T cells remain responsive to B7 stimulation and raise the possibility that B7 antagonists have a role in the prevention/treatment of inflammatory bowel disease.
白细胞介素2(IL-2)缺陷(IL-2-/-)小鼠会发生溶血性贫血和慢性炎症性肠病。重要的是,IL-2缺陷小鼠中疾病的诱导严重依赖于CD4+T细胞。我们研究了来自IL-2缺陷小鼠的T细胞与B7抗原共刺激的需求。稳定的B7-1或B7-2中国仓鼠卵巢(CHO)细胞转染子可与抗CD3单克隆抗体(mAb)协同作用,诱导IL-2-/-突变小鼠的CD4+T细胞增殖。进一步的机制研究表明,B7诱导的激活导致IL-2受体α链的表面表达。B7诱导的增殖独立于IL-4发生,并且在很大程度上独立于IL-2、IL-4、IL-7、IL-9和IL-15受体的共同γ链。最后,在同基因抗原呈递细胞存在的情况下,抗B7-2单克隆抗体而非抗B7-1单克隆抗体能够抑制抗CD3单克隆抗体诱导的IL-2-/-T细胞的激活。我们的实验结果表明,IL-2-/-CD4+T细胞对B7刺激仍有反应,并增加了B7拮抗剂在预防/治疗炎症性肠病中发挥作用的可能性。