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过继性细胞转移疗法治疗转移性黑色素瘤。

Adoptive cell transfer in the treatment of metastatic melanoma.

作者信息

Straten Per thor, Becker Jürgen C

机构信息

Center for Cancer Immune Therapy, Department of Hematology, Herlev University Hospital, Herlev, Denmark.

出版信息

J Invest Dermatol. 2009 Dec;129(12):2743-5. doi: 10.1038/jid.2009.204.

DOI:10.1038/jid.2009.204
PMID:19901944
Abstract

Adoptive cell therapy (ACT) for metastatic cancer is the focus of considerable research effort. Rosenberg's laboratory demonstrated a 50% response rate in stage IV melanoma patients treated with in vitro expanded tumor-infiltrating lymphocytes (TILs) and high-dose IL-2 administered after nonmyeloablative conditioning (Dudley et al., 2002a). Because early attempts to use expanded TILs in melanoma therapy failed to demonstrate better efficacy than high-dose IL-2 (Rosenberg et al., 1994), the efficacy of TILs and nonmyeloablative conditioning in combination implies that patient conditioning is crucial to clinical success. The 2002 data represent a milestone in cellular cancer therapy and a turning point for ACT in cancer treatment.

摘要

转移性癌症的过继性细胞疗法(ACT)是大量研究工作的重点。罗森伯格实验室证明,接受非清髓性预处理后给予体外扩增的肿瘤浸润淋巴细胞(TIL)和高剂量白细胞介素-2治疗的IV期黑色素瘤患者,缓解率达50%(达德利等人,2002年a)。由于早期在黑色素瘤治疗中使用扩增TIL的尝试未能证明其疗效优于高剂量白细胞介素-2(罗森伯格等人,1994年),TIL与非清髓性预处理联合使用的疗效表明,患者预处理对临床成功至关重要。2002年的数据代表了细胞癌症治疗的一个里程碑,也是ACT在癌症治疗中的一个转折点。

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引用本文的文献

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Cancer Immunol Immunother. 2015 Jul;64(7):805-15. doi: 10.1007/s00262-015-1691-7. Epub 2015 Apr 7.
2
Towards neuroimmunotherapy for cancer: the neurotransmitters glutamate, dopamine and GnRH-II augment substantially the ability of T cells of few head and neck cancer patients to perform spontaneous migration, chemotactic migration and migration towards the autologous tumor, and also elevate markedly the expression of CD3zeta and CD3epsilon TCR-associated chains.迈向癌症的神经免疫疗法:神经递质谷氨酸、多巴胺和GnRH-II可显著增强少数头颈癌患者T细胞的自发迁移、趋化迁移以及向自体肿瘤迁移的能力,还能显著提高CD3ζ和CD3ε TCR相关链的表达。
J Neural Transm (Vienna). 2014 Aug;121(8):1007-27. doi: 10.1007/s00702-014-1242-y. Epub 2014 Jul 17.
3
Costimulation through the CD137/4-1BB pathway protects human melanoma tumor-infiltrating lymphocytes from activation-induced cell death and enhances antitumor effector function.CD137/4-1BB 通路共刺激可保护人黑色素瘤肿瘤浸润淋巴细胞免于激活诱导的细胞死亡,并增强抗肿瘤效应功能。
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