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粒细胞输注后脐血CD8 + T细胞扩增可根除难治性白血病。

Cord blood CD8+ T-cell expansion following granulocyte transfusions eradicates refractory leukemia.

作者信息

Hiwarkar Prashant, Adams Stuart, Gilmour Kimberly, Nataraj Ramya, Bonney Denise, Poulton Kay, Wynn Robert

机构信息

Department of Bone Marrow Transplantation, Royal Manchester Children's Hospital, Manchester, United Kingdom.

Department of Bone Marrow Transplantation, Bai Jerbai Wadia Hospital for Children, Mumbai, India.

出版信息

Blood Adv. 2020 Sep 8;4(17):4165-4174. doi: 10.1182/bloodadvances.2020001737.

DOI:10.1182/bloodadvances.2020001737
PMID:32886752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7479944/
Abstract

The action of hematopoietic cell transplantation in controlling leukemia is principally mediated by donor T cells directed against residual recipient malignant cells. However, its utility is limited by graft-versus-host disease (GVHD), where alloreactivity is extended beyond leukemic and marrow cells. In a human/murine chimeric model, we previously showed that the preferential infiltration of cord blood (CB) CD8+ T cells eradicates an Epstein-Barr virus-driven lymphoblastoid tumor without causing xenogeneic GVHD. In the clinic, however, cord blood CD8+ T-cell reconstitution is significantly delayed, and the observation of such a robust antileukemia effect mediated by cord blood CD8+ T cells has not been reported. We describe an observation of very early T-cell expansion in 4 high-risk pediatric leukemia patients receiving third-party, pooled granulocytes after T cell-replete CB transplantation (CBT). The T-cell expansion was transient but robust, including expansion of CD8+ T cells, in contrast to the delayed CD8+ T-cell expansion ordinarily observed after T cell-replete CBT. The CD8+ T cells were polyclonal, rapidly switched to memory phenotype, and had the ability to mediate cytotoxicity. This phenomenon is reproducible, and each patient remains in long-term remission without GVHD. The results suggest that fetal-derived CB CD8+ T cells can be exploited to generate robust antileukemia effects without GVHD.

摘要

造血细胞移植控制白血病的作用主要由针对残留受体恶性细胞的供体T细胞介导。然而,其效用受到移植物抗宿主病(GVHD)的限制,在这种疾病中,同种异体反应性超出了白血病细胞和骨髓细胞的范围。在一个人/鼠嵌合模型中,我们先前表明,脐血(CB)CD8+T细胞的优先浸润可根除爱泼斯坦-巴尔病毒驱动的淋巴母细胞瘤,而不会引起异种GVHD。然而,在临床上,脐血CD8+T细胞重建明显延迟,并且尚未有关于脐血CD8+T细胞介导如此强大的抗白血病作用的观察报道。我们描述了在4例接受T细胞充足的CB移植(CBT)后接受第三方混合粒细胞的高危儿科白血病患者中观察到的非常早期的T细胞扩增。与通常在T细胞充足的CBT后观察到的延迟的CD8+T细胞扩增相反,T细胞扩增是短暂但强烈的,包括CD8+T细胞的扩增。CD8+T细胞是多克隆的,迅速转变为记忆表型,并具有介导细胞毒性的能力。这种现象是可重复的,并且每个患者都保持长期缓解且无GVHD。结果表明,源自胎儿的CB CD8+T细胞可被利用来产生强大的抗白血病作用而无GVHD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d8/7479944/81a6665e57fe/advancesADV2020001737absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d8/7479944/81a6665e57fe/advancesADV2020001737absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d8/7479944/81a6665e57fe/advancesADV2020001737absf1.jpg

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