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白血病的T细胞疗法。

T-cell therapy of leukemia.

作者信息

Riddell Stanley R, Murata Makoto, Bryant Sophia, Warren Edis H

机构信息

Immunology Program, Fred Hutchinson Cancer Research Center, Seattle WA 98109, USA.

出版信息

Cancer Control. 2002 Mar-Apr;9(2):114-22. doi: 10.1177/107327480200900204.

Abstract

BACKGROUND

The demonstration that immune-mediated elimination of leukemia contributes to the success of allogeneic hematopoietic stem cell transplantation (HSCT) has renewed interest in the development of immune-based therapies that might be used to augment the antileukemic effect of HSCT or in patients who are not receiving HSCT.

METHODS

The authors reviewed studies that have analyzed the mechanisms that may be operative in T-cell recognition of leukemia after allogeneic HSCT, identified candidate target antigens for immunotherapy of leukemia in transplant and nontransplant patients, and evaluated expression of candidate antigens on leukemic progenitors.

RESULTS

A large number of potential targets for T-cell therapy or vaccination have now been identified in human leukemia. Studies to evaluate novel immune-based therapies are now being initiated.

CONCLUSIONS

The rapid pace of progress in cellular and molecular immunology has identified new opportunities for developing T-cell therapy or vaccination for leukemia. Obstacles must be addressed before these approaches can be applied broadly, but the promising results of preclinical studies suggest continued efforts in this area will result in the establishment of immunotherapy as a useful modality in clinical practice.

摘要

背景

免疫介导的白血病清除对异基因造血干细胞移植(HSCT)成功的证明,重新激发了人们对开发基于免疫的疗法的兴趣,这些疗法可用于增强HSCT的抗白血病作用,或用于未接受HSCT的患者。

方法

作者回顾了分析异基因HSCT后T细胞识别白血病可能起作用的机制的研究,确定了移植和非移植患者白血病免疫治疗的候选靶抗原,并评估了候选抗原在白血病祖细胞上的表达。

结果

现已在人类白血病中确定了大量T细胞治疗或疫苗接种的潜在靶点。目前正在开展评估新型免疫疗法的研究。

结论

细胞和分子免疫学的快速发展为开发白血病T细胞治疗或疫苗接种带来了新机遇。在这些方法能够广泛应用之前,必须解决一些障碍,但临床前研究的良好结果表明,在这一领域持续努力将使免疫疗法成为临床实践中的一种有用模式。

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