Establishment and Large-scale Expansion of Minimally cultured “Young” Tumor Infiltrating Lymphocytes for Adoptive Transfer Therapy

肿瘤浸润淋巴细胞 过继性细胞移植 黑色素瘤 过继免疫治疗 CD8型 医学 年轻人 癌症 耐火材料(行星科学) 细胞疗法 内科学 肿瘤科 免疫疗法 癌症研究 免疫学 T细胞 免疫系统 细胞 生物 天体生物学 遗传学
作者
Orit Itzhaki,Einat Hovav,Yaara Ziporen,Daphna Levy,Adva Kubi,Dragoslav Zikich,Liat Hershkovitz,Avraham J. Treves,Bruria Shalmon,Douglas Zippel,Gal Markel,Ronnie Shapira‐Frommer,Jacob Schachter,Michal J. Besser
出处
期刊:Journal of Immunotherapy [Ovid Technologies (Wolters Kluwer)]
卷期号:34 (2): 212-220 被引量:172
标识
DOI:10.1097/cji.0b013e318209c94c
摘要

Treatment of metastatic melanoma patients with adoptively transferred tumor infiltrating lymphocytes (TIL) has developed into an effective therapy. Various studies reported objective responses of 50% and more. The use of unselected, minimally cultured, bulk TIL (Young-TIL) has simplified the TIL production process and may therefore, allow the accessibility of this approach to cancer centers worldwide. This article describes the precise process leading to the large-scale production of Young-TIL for therapy. We have enrolled 55 melanoma patients and optimized their Young-TIL generation process. Young-TIL cultures were successfully established for 51 of 55 (93%) patients in 16.7 ± 5.5 days. In a large-scale expansion procedure Young-TIL of 32 patients were further expanded to treatment levels, resulting in a final number of 4.5 x 10¹⁰ ± 2.0 x 10¹⁰ TIL. Fifteen of 31 (48%) patients, who were evaluated, achieved a clinical response, including 4 complete and 11 partial responses. We confirmed the significant correlation between short culture duration, high number of infused cells, and tumor regression. A high percentage of CD8 T cells in the infusion product was beneficial to achieve an objective response. All responding patients were treated with Young-TIL cultures established in < 20 days. In summary, we describe here an efficient and reliable method to generate Young-TIL for adoptive transfer therapy, which may easily be adopted by other cancer centers and can lead to objective responses in 50% of refractory melanoma patients. In the future this approach may be used also in other types of malignancies.
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