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4-1BB-based isolation and expansion of CD8+ T cells specific for self-tumor and non-self-tumor antigens for adoptive T-cell therapy.
Choi, Beom K; Lee, Sang C; Lee, Myoung J; Kim, Young H; Kim, Young-Woo; Ryu, Keun-Won; Lee, Jun-Ho; Shin, Su M; Lee, Sang-Ho; Suzuki, Susumu; Oh, Ho S; Kim, Chang H; Lee, Don G; Hwang, Sun H; Yu, Eun-Mi; Lee, In O; Kwon, Byoung S.
  • Choi BK; *Immune & Cell Therapy Branch, Division of Cancer Biology ‡Biomedicine Production Branch §Center for Gastric Cancer, National Cancer Center, Goyang †Personalized Medicine System R&D Center, Bio-Support Co., Ltd, Gwanyang, Dongan, Anyang, Gyeonggi ∥Department of Surgery, Kosin University College of Medicine, Busan, Korea ¶T Cell Technologies Inc., Nagoya, Aichi, Japan #Section of Clinical Immunology, Allergy, and Rheumatology, Department of Medicine, Tulane University Health Sciences Cent
J Immunother ; 37(4): 225-36, 2014 May.
Article en En | MEDLINE | ID: mdl-24714356
ABSTRACT
Adoptive T-cell therapy is a promising approach to the immunotherapy of cancer, but for it to be a general cancer therapy a simple and standardized procedure for producing tumor-specific CD8 T cells is needed. On the basis of a unique property of 4-1BB (CD137), the selective expression on activated T cells, we have developed a simple and practical protocol to produce antigen-specific CD8 T cells from peripheral blood mononuclear cells. We have proved the feasibility of this procedure by isolating and expanding cytomegalovirus-specific CD8 T cells, and applied the procedure to produce Epstein-Barr virus (EBV)-specific CD8 T cells. By using this procedure, we could readily produce 10-10 antigen-specific CD8 T cells from 30 to 50 mL of blood in about 4 weeks. Moreover, our protocol allowed us to produce, from solid cancer patients, CD8 T cells that were specific for self/tumor antigens such as human telomerase reverse transcriptase (hTERT). It is interesting to note that, we were unable to amplify hTERT-specific CD8 T cells from healthy donors. Our protocol can be readily translated into cGMP-compliant production and is currently being used to produce EBV-specific CD8 T cells for phase I clinical trial. We believe that our method will provide a practical and effective option for adoptive T-cell therapy in the clinic.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Autoantígenos / Inmunoterapia Adoptiva / Linfocitos T CD8-positivos / Miembro 9 de la Superfamilia de Receptores de Factores de Necrosis Tumoral / Antígenos de Neoplasias / Neoplasias Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Autoantígenos / Inmunoterapia Adoptiva / Linfocitos T CD8-positivos / Miembro 9 de la Superfamilia de Receptores de Factores de Necrosis Tumoral / Antígenos de Neoplasias / Neoplasias Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Año: 2014 Tipo del documento: Article