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利用有益的同种异体反应性T细胞。

Exploiting beneficial alloreactive T cells.

作者信息

Barber L D, Madrigal J A

机构信息

The Anthony Nolan Research Institute, Royal Free Hospital, Pond Street, Hampstead, London, UK.

出版信息

Vox Sang. 2006 Jul;91(1):20-7. doi: 10.1111/j.1423-0410.2006.00775.x.

DOI:10.1111/j.1423-0410.2006.00775.x
PMID:16756597
Abstract

Although the T-cell response to allogeneic cells is typically regarded as a detrimental phenomenon responsible for rejection of transplanted allografts and graft-vs.-host disease following haematopoietic stem cell transplantation, beneficial components also exist within the alloreactive population. Alloreactive T cells specific for tumour antigens can contribute to the elimination of malignant cells, and alloantigen-specific regulatory T cells can promote transplant tolerance. The challenge is to separate the good from the bad. We review how the identification, isolation and manipulation of beneficial alloreactive T cells has grown from a greater understanding of the molecular basis of the T-cell alloresponse and how alloaggression could be exploited for immunotherapy.

摘要

尽管对同种异体细胞的T细胞反应通常被视为一种有害现象,它会导致移植的同种异体移植物被排斥以及造血干细胞移植后发生移植物抗宿主病,但同种反应性群体中也存在有益成分。对肿瘤抗原有特异性的同种反应性T细胞有助于消除恶性细胞,而异种抗原特异性调节性T细胞可促进移植耐受。挑战在于区分好坏。我们回顾了对有益同种反应性T细胞的鉴定、分离和操控是如何基于对T细胞同种反应分子基础的更深入理解而发展起来的,以及同种攻击如何能够被用于免疫治疗。

相似文献

1
Exploiting beneficial alloreactive T cells.利用有益的同种异体反应性T细胞。
Vox Sang. 2006 Jul;91(1):20-7. doi: 10.1111/j.1423-0410.2006.00775.x.
2
Cytolytic pathways in haematopoietic stem-cell transplantation.造血干细胞移植中的细胞溶解途径。
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Haematopoietic cell transplantation as immunotherapy.造血细胞移植作为免疫疗法。
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4
Alloreactivity as therapeutic principle in the treatment of hematologic malignancies. Studies of clinical and immunologic aspects of allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning.异基因反应性作为血液系统恶性肿瘤治疗的治疗原则。非清髓性预处理的异基因造血细胞移植的临床和免疫学方面的研究。
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Ex vivo selection of recipient-type alloantigen-specific CD4(+)CD25(+) immunoregulatory T cells for the control of graft-versus-host disease after allogeneic hematopoietic stem-cell transplantation.体外选择受者型同种异体抗原特异性CD4(+)CD25(+)免疫调节性T细胞,用于控制异基因造血干细胞移植后的移植物抗宿主病
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Induction of acute graft-versus-host disease by T cells that do not respond to in vitro alloantigen stimulation.对体外同种异体抗原刺激无反应的T细胞诱导急性移植物抗宿主病。
Br J Haematol. 2004 Sep;126(6):828-36. doi: 10.1111/j.1365-2141.2004.05131.x.
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Minor histocompatibility antigens: targets for tumour therapy and transplant tolerance.次要组织相容性抗原:肿瘤治疗和移植耐受的靶点
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Minors come of age: Minor histocompatibility antigens and graft-versus-host disease.未成年人成年:次要组织相容性抗原与移植物抗宿主病。
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引用本文的文献

1
A phase I trial of adoptive transfer of allogeneic natural killer cells in patients with advanced non-small cell lung cancer.一项异体自然杀伤细胞过继转移治疗晚期非小细胞肺癌的 I 期临床试验。
Cancer Immunol Immunother. 2010 Dec;59(12):1781-9. doi: 10.1007/s00262-010-0904-3. Epub 2010 Aug 12.
2
Dendritic cell function during chronic hepatitis C virus and human immunodeficiency virus type 1 infection.慢性丙型肝炎病毒和1型人类免疫缺陷病毒感染期间树突状细胞的功能
Clin Vaccine Immunol. 2007 Sep;14(9):1127-37. doi: 10.1128/CVI.00141-07. Epub 2007 Jul 18.
3
Semi-allogeneic dendritic cells can induce antigen-specific T-cell activation, which is not enhanced by concurrent alloreactivity.
半同种异体树突状细胞可诱导抗原特异性T细胞活化,同时存在的同种异体反应性并不会增强这种活化。
Cancer Immunol Immunother. 2007 Dec;56(12):1861-73. doi: 10.1007/s00262-007-0328-x. Epub 2007 May 9.
4
Clonotypic analysis of T cell reconstitution after haematopoietic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency.严重联合免疫缺陷患者造血干细胞移植(HSCT)后T细胞重建的克隆型分析。
Clin Exp Immunol. 2007 Jun;148(3):450-60. doi: 10.1111/j.1365-2249.2007.03378.x. Epub 2007 Mar 21.