Thangavelu Govindarajan, Anderson Colin C
Departments of Surgery and Medical Microbiology and Immunology, and Alberta Diabetes Institute; University of Alberta; Edmonton, AB Canada.
Chimerism. 2011 Jan;2(1):29-32. doi: 10.4161/chim.2.1.15083.
One of the main objectives in allogeneic hematopoietic stem cell transplantation (aHSCT) research is the prevention of graft versus host disease (GVHD) while maintaining the graft versus leukemia/lymphoma (GVL) effect. Whether these two responses generated by donor T cells can be sufficiently separated and controlled remains controversial. While various approaches have been tested to achieve this goal, success has been relatively limited. Lymphocyte responses are negatively regulated by a series of receptors that function along with antigen receptors to deliver co-inhibitory signals. B and T lymphocyte associated (BTLA) is a novel co-inhibitory molecule expressed by activated T cells, B cells and other immune cells. A study by Albring et al. has now shown in a murine model that a single injection of agonistic anti-BTLA monoclonal antibody can inhibit GVHD long-term while maintaining GVL responses and immunity to infection. These studies suggest that future development of biologics to harness the function of co-inhibitory signals will be an important approach in the prevention of autoimmunity and GVHD and in protocols to achieve transplantation tolerance.
异基因造血干细胞移植(aHSCT)研究的主要目标之一是预防移植物抗宿主病(GVHD),同时维持移植物抗白血病/淋巴瘤(GVL)效应。供体T细胞产生的这两种反应是否能够充分分离和控制仍存在争议。虽然已经测试了各种方法来实现这一目标,但成功相对有限。淋巴细胞反应受到一系列受体的负调控,这些受体与抗原受体共同发挥作用,传递共抑制信号。B和T淋巴细胞相关分子(BTLA)是一种由活化T细胞、B细胞和其他免疫细胞表达的新型共抑制分子。Albring等人的一项研究现已在小鼠模型中表明,单次注射激动性抗BTLA单克隆抗体可长期抑制GVHD,同时维持GVL反应和抗感染免疫力。这些研究表明,未来开发利用共抑制信号功能的生物制剂将是预防自身免疫和GVHD以及实现移植耐受方案的重要途径。