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Virotherapy Using Myxoma Virus Prevents Lethal Graft-versus-Host Disease following Xeno-Transplantation with Primary Human Hematopoietic Stem Cells

机译:病毒疗法使用粘液瘤病毒防止致命的移植物抗宿主病以下异种移植原发性人类造血干细胞

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摘要

Graft-versus-host disease (GVHD) is a potentially lethal clinical complication arising from the transfer of alloreactive T lymphocytes into immunocompromised recipients. Despite conventional methods of T cell depletion, GVHD remains a major challenge in allogeneic hematopoietic cell transplant. Here, we demonstrate a novel method of preventing GVHD by ex vivo treatment of primary human hematopoietic cell sources with myxoma virus, a rabbit specific poxvirus currently under development for oncolytic virotherapy. This pretreatment dramatically increases post-transplant survival of immunocompromised mice injected with primary human bone marrow or peripheral blood cells and prevents the expansion of human CD3+ lymphocytes in major recipient organs. Similar viral treatment also prevents human-human mixed alloreactive T lymphocyte reactions in vitro. Our data suggest that ex vivo virotherapy with myxoma virus can be a simple and effective method for preventing GVHD following infusion of hematopoietic products containing alloreactive T lymphocytes such as: allogeneic hematopoietic stem and progenitor cells, donor leukocyte infusions and blood transfusions.
机译:移植物抗宿主病(GVHD)是由于将同种反应性T淋巴细胞转移至免疫功能低下的受体而引起的潜在致命性临床并发症。尽管有常规的T细胞清除方法,但GVHD仍是同种异体造血细胞移植中的主要挑战。在这里,我们展示了一种通过粘液瘤病毒(一种目前正在开发溶瘤病毒疗法的兔特异性痘病毒)离体治疗原代人造血细胞源来预防GVHD的新方法。这种预处理极大地增加了注射原代人骨髓或外周血细胞的免疫受损小鼠的移植后存活率,并防止了主要受体器官中人CD3 + 淋巴细胞的扩增。相似的病毒治疗也可以防止人与人混合的异源性T淋巴细胞体外反应。我们的数据表明,粘液瘤病毒的离体病毒疗法可以是一种简单而有效的方法,用于预防输注含有同种异体反应性T淋巴细胞的造血产物,例如同种异体造血干细胞和祖细胞,供体白细胞输注和输血。

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