Field Elizabeth H, Kulhankova Katarina, Nasr Mohamed E
Department of Medicine, Division of Rheumatology, Roy J and Lucille A Carver College of Medicine, Iowa City, IA, USA.
Immunol Res. 2007;39(1-3):62-78. doi: 10.1007/s12026-007-0064-5.
The natural CD4+CD25+ T regulatory (Treg) lymphocyte has emerged as a critical cell for controlling immune responses to self, foreign proteins, and pathogens. Identified initially by the constitutive expression of CD4 and CD25, natural Tregs suppress a variety of immune cells and responses, including CD4+CD25- proliferation and IL-2 production, and CD8 cell proliferation, IFNgamma production and CTL activity. Although natural Tregs require activation with specific antigen to attain their suppressive phenotype, once activated they execute inhibition in an antigen specific as well as non-specific (bystander) fashion. Treg suppression depends on IL-2, CD25, and cell:cell contact. The use of live cell imaging in vivo and in vitro to visualize the dynamic cell:cell interactions involving natural Tregs as well as the CD4+CD25+ Treg inhibitory hybridoma RD6 has refined the mechanistic models of contact dependent Treg suppression.
天然CD4+CD25+调节性T(Treg)淋巴细胞已成为控制针对自身、外来蛋白质和病原体的免疫反应的关键细胞。天然Tregs最初通过CD4和CD25的组成性表达得以识别,它可抑制多种免疫细胞和免疫反应,包括CD4+CD25-细胞的增殖和白细胞介素-2的产生,以及CD8细胞的增殖、γ干扰素的产生和细胞毒性T淋巴细胞(CTL)活性。尽管天然Tregs需要通过特定抗原激活才能获得其抑制表型,但一旦被激活,它们就会以抗原特异性以及非特异性(旁观者)方式执行抑制作用。Treg抑制作用依赖于白细胞介素-2、CD25和细胞间接触。运用体内和体外活细胞成像技术来观察涉及天然Tregs以及CD4+CD25+ Treg抑制性杂交瘤RD6的动态细胞间相互作用,完善了接触依赖性Treg抑制作用的机制模型。