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WT1 Pulsed Human CD141+ Dendritic Cell Vaccine Has High Potential in Solid Tumor-Targeted Immunotherapy.
Cho, Sung Yoon; Jeong, Seong Mun; Jeon, Young Joo; Yang, Sun Ja; Hwang, Ju Eun; Yoo, Byung Moo; Kim, Hyun Soo.
Afiliação
  • Cho SY; R&D Center, Pharmicell Co., Ltd., Seongnam 13229, Republic of Korea.
  • Jeong SM; R&D Center, Pharmicell Co., Ltd., Seongnam 13229, Republic of Korea.
  • Jeon YJ; R&D Center, Pharmicell Co., Ltd., Seongnam 13229, Republic of Korea.
  • Yang SJ; R&D Center, Pharmicell Co., Ltd., Seongnam 13229, Republic of Korea.
  • Hwang JE; Dr. Kim's Stem Cell Clinic, 874 Eonju-ro Gangnam, Seoul 06027, Republic of Korea.
  • Yoo BM; Department of Gastroenterology, Ajou University School of Medicine, Worldcup-ro 164, Youngtong-gu, Suwon 16499, Republic of Korea.
  • Kim HS; R&D Center, Pharmicell Co., Ltd., Seongnam 13229, Republic of Korea.
Int J Mol Sci ; 24(2)2023 Jan 12.
Article em En | MEDLINE | ID: mdl-36675017
ABSTRACT
Dendritic cells (DC) are powerful cells that play critical roles in anti-tumor immunity, and their use in cancer immunotherapy unlocks hidden capabilities as an effective therapeutic. In order to maximize the full potential of DC, we developed a DC vaccine named CellgramDC-WT1 (CDW). CDW was pulsed with WT1, an antigen commonly expressed in solid tumors, and induced with zoledronate to aid DC maturation. Although our previous study focused on using Rg3 as an inducer of DC maturation, problems with quality control and access led us to choose zoledronate as a better alternative. Furthermore, CDW secreted IL-12 and IFN-γ, which induced the differentiation of naïve T cells to active CD8+ T cells and elicited cytotoxic T lymphocyte (CTL) response against cancer cells with WT1 antigens. By confirming the identity and function of CDW, we believe CDW is an improved DC vaccine and holds promising potential in the field of cancer immunotherapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas / Vacinas Anticâncer / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas / Vacinas Anticâncer / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article