Focus on Adoptive T Cell Transfer Trials in Melanoma

被引:31
作者
Hershkovitz, Liat [1 ]
Schachter, Jacob [1 ]
Treves, Avraham J. [2 ]
Besser, Michal J. [1 ,3 ]
机构
[1] Chaim Sheba Med Ctr, Ella Inst Melanoma, IL-52621 Tel Hashomer, Israel
[2] Chaim Sheba Med Ctr, Sheba Canc Res Ctr, IL-52621 Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Sch Med, Dept Human Microbiol & Immunol, IL-69978 Tel Aviv, Israel
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2010年
关键词
TUMOR-INFILTRATING LYMPHOCYTES; DOSE RECOMBINANT INTERLEUKIN-2; ACTIVATED KILLER-CELLS; IN-VIVO PERSISTENCE; METASTATIC MELANOMA; CANCER REGRESSION; TRANSFER THERAPY; CUTTING EDGE; LAK CELLS; IMMUNOTHERAPY;
D O I
10.1155/2010/260267
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adoptive Cell Transfer (ACT) of Tumor-Infiltrating Lymphocytes (TIL) in combination with lymphodepletion has proven to be an effective treatment for metastatic melanoma patients, with an objective response rate in 50%-70% of the patients. It is based on the ex vivo expansion and activation of tumor-specific T lymphocytes extracted from the tumor and their administration back to the patient. Various TIL-ACT trials, which differ in their TIL generation procedures and patient preconditioning, have been reported. In the latest clinical studies, genetically engineered peripheral T cells were utilized instead of TIL. Further improvement of adoptive T cell transfer depends on new investigations which seek higher TIL quality, increased durable response rates, and aim to treat more patients. Simplifying this therapy may encourage cancer centers worldwide to adopt this promising technology. This paper focuses on the latest progress regarding adoptive T cell transfer, comparing the currently available protocols and discussing their advantages, disadvantages, and implication in the future.
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页数:11
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