Mueller D L, Chiodetti L, Bacon P A, Schwartz R H
Harold C. Simmons Arthritis Research Center, Dallas, TX.
J Immunol. 1991 Dec 15;147(12):4118-25.
In this report we extend the in vitro clonal anergy model to examine the regulation of proliferation in T cells that secrete both IL-2 and IL-4. Newly cloned Ag-specific murine T cells are shown to depend on both IL-2 and IL-4 synthesis for maximal proliferation. Whereas IL-2 responsiveness is constitutive in these cells, IL-4 responsiveness develops only after Ag and APC stimulation. Remarkably, proliferation of these cells to Ag is sensitive to inhibition by clonal anergy, even though IL-4 synthesis remains inducible. Anergy in these cells is associated with an inability to respond to IL-4, in addition to the development of an IL-2 production defect. The results suggest that anergy induction may be capable of preventing the clonal expansion of autoreactive T cells producing both IL-2 and IL-4 in vivo.
在本报告中,我们扩展了体外克隆无能模型,以研究分泌白细胞介素-2(IL-2)和白细胞介素-4(IL-4)的T细胞的增殖调控。新克隆的抗原特异性小鼠T细胞显示,最大程度的增殖依赖于IL-2和IL-4的合成。虽然这些细胞对IL-2的反应性是组成性的,但IL-4反应性仅在抗原和抗原呈递细胞(APC)刺激后才发展。值得注意的是,尽管IL-4的合成仍可诱导,但这些细胞对抗原的增殖对克隆无能的抑制敏感。这些细胞中的无能除了产生IL-2缺陷外,还与无法对IL-4作出反应有关。结果表明,无能诱导可能能够在体内阻止产生IL-2和IL-4的自身反应性T细胞的克隆扩增。