Jian You-Qiang, Ye Jian, Qi Hui, Deng Chun-Yan, Deng Shao-Ping, Li Fu-Rong
Department of General surgery, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen, China.
The Key Laboratory of stem cell and Cellular therapy, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen, China.
Immunol Cell Biol. 2017 Feb;95(2):189-197. doi: 10.1038/icb.2016.88. Epub 2016 Sep 12.
Donor-reactive memory T (Tm)cells mediate accelerated rejection, which is known as a barrier to the survival of transplanted organs. Selective interference with the anti-CD45RB monoclonal antibody (α-CD45RB) reliably induces donor-specific tolerance. In this study, pre-sensitization to female C57BL/6 mice with the skin of female BLAB/c mice generated a large number of Tm cells and resulted in rapid rejection of the secondly transplanted allografts. α-CD45RB did induce the tolerance to skin allograft primarily transplanted but failed to induce tolerance in the pre-sensitized mice. Donor-specific spleen cell transfusion (DST) alone also failed to induce the tolerance in the pre-sensitized recipients. Interestingly, combination of α-CD45RB with DST inhibited the rejection induced by memory T cells in the pre-sensitized mice. CD25+ T-cell depletion in α-CD45RB combined with DST therapy recipients could prevent skin allograft tolerance from establishing. In addition, adoptive transfer of donor-primed memory T cells into the tolerant recipients markedly broke the established tolerance. Our findings indicate that α-CD45RB and DST can synergistically inhibit the accelerated rejection mediated by memory T cells and induce long-term skin allograft acceptance in mice.
供体反应性记忆T(Tm)细胞介导加速排斥反应,这是移植器官存活的一个障碍。抗CD45RB单克隆抗体(α-CD45RB)的选择性干扰可可靠地诱导供体特异性耐受。在本研究中,用雌性BLAB/c小鼠的皮肤对雌性C57BL/6小鼠进行预致敏,产生了大量Tm细胞,并导致二次移植的同种异体移植物快速排斥。α-CD45RB确实诱导了对初次移植皮肤同种异体移植物的耐受,但未能在预致敏小鼠中诱导耐受。单独的供体特异性脾细胞输注(DST)也未能在预致敏受体中诱导耐受。有趣的是,α-CD45RB与DST联合使用可抑制预致敏小鼠中记忆T细胞诱导的排斥反应。α-CD45RB联合DST治疗的受体中CD25 + T细胞的清除可阻止皮肤同种异体移植物耐受的建立。此外,将供体启动的记忆T细胞过继转移到耐受受体中可明显打破已建立的耐受。我们的研究结果表明,α-CD45RB和DST可协同抑制记忆T细胞介导的加速排斥反应,并诱导小鼠长期接受皮肤同种异体移植物。