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异基因造血干细胞移植中自然杀伤细胞的功能重建

Functional Reconstitution of Natural Killer Cells in Allogeneic Hematopoietic Stem Cell Transplantation.

作者信息

Ullah Md Ashik, Hill Geoffrey R, Tey Siok-Keen

机构信息

Bone Marrow Transplant Laboratory, QIMR Berghofer Medical Research Institute , Brisbane, QLD , Australia.

Bone Marrow Transplant Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia; Department of Haematology and Bone Marrow Transplantation, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.

出版信息

Front Immunol. 2016 Apr 15;7:144. doi: 10.3389/fimmu.2016.00144. eCollection 2016.

Abstract

Natural killer (NK) cells are the first lymphocyte population to reconstitute following allogeneic hematopoietic stem cell transplantation (HSCT) and are important in mediating immunity against both leukemia and pathogens. Although NK cell numbers generally reconstitute within a month, the acquisition of mature NK cell phenotype and full functional competency can take 6 months or more, and is influenced by graft composition, concurrent pharmacologic immunosuppression, graft-versus-host disease, and other clinical factors. In addition, cytomegalovirus infection and reactivation have a dominant effect on NK cell memory imprinting following allogeneic HSCT just as it does in healthy individuals. Our understanding of NK cell education and licensing has evolved in the years since the "missing self" hypothesis for NK-mediated graft-versus-leukemia effect was first put forward. For example, we now know that NK cell "re-education" can occur, and that unlicensed NK cells can be more protective than licensed NK cells in certain settings, thus raising new questions about how best to harness graft-versus-leukemia effect. Here, we review current understanding of the functional reconstitution of NK cells and NK cell education following allogeneic HSCT, highlighting a conceptual framework for future research.

摘要

自然杀伤(NK)细胞是异基因造血干细胞移植(HSCT)后最早重建的淋巴细胞群体,在介导抗白血病和病原体免疫方面发挥重要作用。尽管NK细胞数量通常在一个月内重建,但获得成熟NK细胞表型和完全功能能力可能需要6个月或更长时间,并且受移植物组成、同时进行的药物免疫抑制、移植物抗宿主病及其他临床因素影响。此外,巨细胞病毒感染和再激活对异基因HSCT后的NK细胞记忆印记具有主导作用,这与在健康个体中情况相同。自从首次提出NK介导的移植物抗白血病效应的“缺失自我”假说以来,我们对NK细胞教育和许可的理解在这些年里不断发展。例如,我们现在知道NK细胞“再教育”可以发生,并且在某些情况下,未获得许可的NK细胞可能比获得许可的NK细胞更具保护作用,从而引发了关于如何最好地利用移植物抗白血病效应的新问题。在此,我们综述了目前对异基因HSCT后NK细胞功能重建和NK细胞教育的理解,突出了未来研究的概念框架。

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