R707, a fully human antibody directed against CC-chemokine receptor 7, attenuates xenogeneic acute graft-versus-host disease

被引:7
|
作者
Fowler, Kenneth A. [1 ]
Vasilieva, Viktoria [2 ]
Ivanova, Ekaterina [2 ]
Rimkevich, Olga [2 ]
Sokolov, Andrey [2 ,4 ]
Abbasova, Svetlana [2 ]
Kim, Eldar [2 ]
Coghill, James M. [1 ,3 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA
[2] MSM Prot Technol, Waltham, MA USA
[3] Univ N Carolina, Dept Med, Chapel Hill, NC 27515 USA
[4] Russian Acad Sci, Pushchino Res Ctr, Inst Biol Instrumentat, Moscow, Russia
关键词
animal models; murine; bone marrow; hematopoietic stem cell transplantation; chemokines; chemokine receptors; graft-versus-host disease (GVHD); graft-versus-leukemia (GVL); graft versus tumor; hematology; oncology; immunosuppressant; immunosuppression; immune modulation; translational research; science; MEMORY T-CELLS; PREVENTION; INCREASES; SEVERITY; NAIVE; MODEL;
D O I
10.1111/ajt.15298
中图分类号
R61 [外科手术学];
学科分类号
摘要
Acute graft-versus-host disease (aGVHD) remains a barrier to the success of allogeneic hematopoietic stem cell transplantation (HSCT). Previously, we demonstrated that CC-chemokine receptor 7 (CCR7) is critical for aGVHD pathogenesis but dispensable for beneficial graft-versus-leukemia responses. As a result, we evaluated a fully human anti-CCR7-blocking antibody as a new approach to prevent aGVHD in preclinical models. Here we report that antibody R707 is able to block human CCR7 signaling and function in vitro in response to its 2 natural ligands. The antibody was less active against the murine orthologue, however, and failed to substantially limit aGVHD in a standard murine allogeneic HSCT model. Nevertheless, R707 significantly reduced xenogeneic aGVHD induced by human peripheral blood mononuclear cells (PBMCs). R707 limited CD4(+) and in particular CD8(+) T cell expansion during the period of antibody administration. These effects were transient, however, and T cell numbers recovered after antibody cessation. R707 did not substantially impair the antitumor potential of the PBMC inoculum as antibody-treated mice retained their capacity to reject a human acute myeloid leukemia cell line. Collectively, these data indicate for the first time that an antibody directed against CCR7 might represent a viable new approach for aGVHD prevention.
引用
收藏
页码:1941 / 1954
页数:14
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