adoptive cell therapy Search Results


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Innovative Therapies adoptive cell immunotherapy
Adoptive Cell Immunotherapy, supplied by Innovative Therapies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Helmholtz Zentrum fur Infektionsforschung GmbH adoptive t cell therapies
Adoptive T Cell Therapies, supplied by Helmholtz Zentrum fur Infektionsforschung GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nature Biotechnology adoptive t-cell therapy (act)
Adoptive T Cell Therapy (Act), supplied by Nature Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sangamo Inc adoptive cell therapies
Adoptive Cell Therapies, supplied by Sangamo Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ProMab Inc adoptive cell therapies
Adoptive Cell Therapies, supplied by ProMab Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Human Protein Atlas act adoptive cell therapy
Act Adoptive Cell Therapy, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novartis adoptive cell therapies
Adoptive Cell Therapies, supplied by Novartis, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioNTech neoantigen-specific adoptive cell therapy
Neoantigen Specific Adoptive Cell Therapy, supplied by BioNTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ACTGene Inc adoptive t cell therapy act
The regulation of PD-1/PD-L1 signaling on immune cells. a . The PD-1/PD-L1 pathway promotes the exhaustion and apoptosis of effector T cells. Tex cells are characterized by increased expression of highly inhibitory receptors, including PD-1, LAG3, and TIGIT, decreased cytokine production such as TNF, IL-2, and IFN-γ, metabolic alterations, and impaired proliferative capacity and survival. b . PD-1/PD-L1 promotes the generation and development of induced Tregs (iTregs) by reducing the phosphorylation of PI3K/Akt/mTOR and S6, while enhancing PTEN, thus enhancing the immune suppression functions of Treg cells and inducing immune tolerance. c . PD-1/PD-L1 can promote the polarization of tumor-associated macrophages (TAM) toward the M2 phenotype, releasing large amounts of fibroblast growth factor, VEGF, TNF-α, and other cytokines to promote angiogenesis and support immune suppression, invasion, and metastasis of cancer cells, accelerating cancer progression. d . PD-1 on NK cells binds to PD-L1 on cancer cells, inhibiting the degranulation and cytotoxic function of NK cells, decreasing their ability to kill tumor cells, and promoting tumor immune escape. The use of PD-1 and PD-L1 <t>inhibitors</t> may reactivate the anti-tumor immune response of the above immune cells. Figure created with BioRender
Adoptive T Cell Therapy Act, supplied by ACTGene Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Lechler GmbH adoptive regulatory t cell therapy
The regulation of PD-1/PD-L1 signaling on immune cells. a . The PD-1/PD-L1 pathway promotes the exhaustion and apoptosis of effector T cells. Tex cells are characterized by increased expression of highly inhibitory receptors, including PD-1, LAG3, and TIGIT, decreased cytokine production such as TNF, IL-2, and IFN-γ, metabolic alterations, and impaired proliferative capacity and survival. b . PD-1/PD-L1 promotes the generation and development of induced Tregs (iTregs) by reducing the phosphorylation of PI3K/Akt/mTOR and S6, while enhancing PTEN, thus enhancing the immune suppression functions of Treg cells and inducing immune tolerance. c . PD-1/PD-L1 can promote the polarization of tumor-associated macrophages (TAM) toward the M2 phenotype, releasing large amounts of fibroblast growth factor, VEGF, TNF-α, and other cytokines to promote angiogenesis and support immune suppression, invasion, and metastasis of cancer cells, accelerating cancer progression. d . PD-1 on NK cells binds to PD-L1 on cancer cells, inhibiting the degranulation and cytotoxic function of NK cells, decreasing their ability to kill tumor cells, and promoting tumor immune escape. The use of PD-1 and PD-L1 <t>inhibitors</t> may reactivate the anti-tumor immune response of the above immune cells. Figure created with BioRender
Adoptive Regulatory T Cell Therapy, supplied by Lechler GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sanquin adoptive t cell therapy
The regulation of PD-1/PD-L1 signaling on immune cells. a . The PD-1/PD-L1 pathway promotes the exhaustion and apoptosis of effector T cells. Tex cells are characterized by increased expression of highly inhibitory receptors, including PD-1, LAG3, and TIGIT, decreased cytokine production such as TNF, IL-2, and IFN-γ, metabolic alterations, and impaired proliferative capacity and survival. b . PD-1/PD-L1 promotes the generation and development of induced Tregs (iTregs) by reducing the phosphorylation of PI3K/Akt/mTOR and S6, while enhancing PTEN, thus enhancing the immune suppression functions of Treg cells and inducing immune tolerance. c . PD-1/PD-L1 can promote the polarization of tumor-associated macrophages (TAM) toward the M2 phenotype, releasing large amounts of fibroblast growth factor, VEGF, TNF-α, and other cytokines to promote angiogenesis and support immune suppression, invasion, and metastasis of cancer cells, accelerating cancer progression. d . PD-1 on NK cells binds to PD-L1 on cancer cells, inhibiting the degranulation and cytotoxic function of NK cells, decreasing their ability to kill tumor cells, and promoting tumor immune escape. The use of PD-1 and PD-L1 <t>inhibitors</t> may reactivate the anti-tumor immune response of the above immune cells. Figure created with BioRender
Adoptive T Cell Therapy, supplied by Sanquin, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TxCell Inc adoptive t-cell therapy

Adoptive T Cell Therapy, supplied by TxCell Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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The regulation of PD-1/PD-L1 signaling on immune cells. a . The PD-1/PD-L1 pathway promotes the exhaustion and apoptosis of effector T cells. Tex cells are characterized by increased expression of highly inhibitory receptors, including PD-1, LAG3, and TIGIT, decreased cytokine production such as TNF, IL-2, and IFN-γ, metabolic alterations, and impaired proliferative capacity and survival. b . PD-1/PD-L1 promotes the generation and development of induced Tregs (iTregs) by reducing the phosphorylation of PI3K/Akt/mTOR and S6, while enhancing PTEN, thus enhancing the immune suppression functions of Treg cells and inducing immune tolerance. c . PD-1/PD-L1 can promote the polarization of tumor-associated macrophages (TAM) toward the M2 phenotype, releasing large amounts of fibroblast growth factor, VEGF, TNF-α, and other cytokines to promote angiogenesis and support immune suppression, invasion, and metastasis of cancer cells, accelerating cancer progression. d . PD-1 on NK cells binds to PD-L1 on cancer cells, inhibiting the degranulation and cytotoxic function of NK cells, decreasing their ability to kill tumor cells, and promoting tumor immune escape. The use of PD-1 and PD-L1 inhibitors may reactivate the anti-tumor immune response of the above immune cells. Figure created with BioRender

Journal: Molecular Cancer

Article Title: Regulatory mechanisms of PD-1/PD-L1 in cancers

doi: 10.1186/s12943-024-02023-w

Figure Lengend Snippet: The regulation of PD-1/PD-L1 signaling on immune cells. a . The PD-1/PD-L1 pathway promotes the exhaustion and apoptosis of effector T cells. Tex cells are characterized by increased expression of highly inhibitory receptors, including PD-1, LAG3, and TIGIT, decreased cytokine production such as TNF, IL-2, and IFN-γ, metabolic alterations, and impaired proliferative capacity and survival. b . PD-1/PD-L1 promotes the generation and development of induced Tregs (iTregs) by reducing the phosphorylation of PI3K/Akt/mTOR and S6, while enhancing PTEN, thus enhancing the immune suppression functions of Treg cells and inducing immune tolerance. c . PD-1/PD-L1 can promote the polarization of tumor-associated macrophages (TAM) toward the M2 phenotype, releasing large amounts of fibroblast growth factor, VEGF, TNF-α, and other cytokines to promote angiogenesis and support immune suppression, invasion, and metastasis of cancer cells, accelerating cancer progression. d . PD-1 on NK cells binds to PD-L1 on cancer cells, inhibiting the degranulation and cytotoxic function of NK cells, decreasing their ability to kill tumor cells, and promoting tumor immune escape. The use of PD-1 and PD-L1 inhibitors may reactivate the anti-tumor immune response of the above immune cells. Figure created with BioRender

Article Snippet: Currently, the therapeutic approaches targeting PD-1/PD-L1 include immune checkpoint inhibitors, adoptive T cell therapy (ACT), gene editing therapies, and tumor vaccines, which have been widely applied clinically in advanced cancer patients, particularly in melanoma and lung cancer, achieving remarkable early success and greatly improving the overall survival and progression-free survival of cancer patients [ ].

Techniques: Expressing, Phospho-proteomics

Journal: Bone Marrow Transplantation

Article Title: The 46 th Annual Meeting of the European Society for Blood and Marrow Transplantation: Physicians Poster Session (P001-P706)

doi: 10.1038/s41409-020-01120-w

Figure Lengend Snippet:

Article Snippet: Chiara Bonini received research founding by Intellia Therapeutics, is owner of patents in the field of adoptive T-cell therapy and is a consultant of Molmed Spa, Intellia therapeutics, TxCell, Novartis, GSK, Allogene and Kite/Gilead.

Techniques: