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autologous tumor lysate-pulsed DC-CIK cells

Development stage
Phase 2
Lead developer
CoImmune
Modality
Lymphokine-Activated Killer Cells → Native Immune Cells → Adoptive Cell Transfer → Cell Therapies, CAR-NK Cells → Other Engineered Cells → Adoptive Cell Transfer → Cell Therapies, Dendritic Cell Vaccines → Immune Effector Cells → Other Cell Types → Cell Therapies
Administration
Intravenous
01

Overview

Autologous tumor lysate-pulsed DC-CIK cells is a personalized adoptive cellular immunotherapy that combines dendritic cells (DCs) pulsed with autologous tumor lysate to prime tumor-specific immunity and cytokine-induced killer (CIK) cells expanded ex vivo to provide cytotoxic effector function. DCs are generated from patient peripheral blood monocytes with GM-CSF and IL-4, then matured and loaded with autologous tumor lysate prepared by freeze–thaw cycles, presenting a broad repertoire of tumor-associated antigens to activate T-cell responses. CIK cells are expanded from patient lymphocytes using anti-CD3, IFN-γ, and IL-2 to yield CD3+CD56+ cytotoxic cells with MHC-unrestricted killing. The combined DC vaccine plus CIK infusion aims to enhance both specificity and cytotoxicity, with reported increases in Th1 cytokines (IL-12, IFN-γ), and has been studied in gastric, colorectal, breast cancers and others, often after low-dose chemotherapy, showing potential improvements in progression-free and overall survival in non-randomized/observational settings and ongoing trials. It is an autologous, ex vivo–manufactured cell therapy rather than a single molecular drug.[3][4][5][1][2][7]

Other names
autologous tumor lysate-pulsed dendritic cell immunotherapy with cytokine-induced killer cellsDC-CIKtumor lysate-pulsed DC-CIKTL-pulsed DC-CIK
02

Targets

NKG receptor (NKG / NK cell receptors)IL-12R (Interleukin-12 receptor)IFNGR1 (Interferon gamma receptor 1)

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