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Neoantigen-Specific Adoptive Cell Therapies for Cancer: Making T-Cell Products More Personal
by
Harari, Alexandre
, Bianchi, Valentina
, Coukos, George
in
adoptive cell therapy (ACT)
/ Animals
/ Antigens
/ Antigens, Neoplasm - immunology
/ Antitumor activity
/ Biomarkers
/ cancer immunotherapy
/ Cell therapy
/ Cells
/ Cells, Cultured
/ Clinical Studies as Topic
/ Coculture Techniques
/ Cytokines - metabolism
/ Cytomegalovirus
/ enrichment
/ Epitopes, T-Lymphocyte - immunology
/ HLA Antigens - immunology
/ Humans
/ Immune response
/ Immunology
/ Immunotherapy
/ Immunotherapy, Adoptive - methods
/ Lymphocyte Activation - immunology
/ Lymphocytes
/ Lymphocytes T
/ Lymphocytes, Tumor-Infiltrating - immunology
/ Lymphocytes, Tumor-Infiltrating - metabolism
/ Major histocompatibility complex
/ Melanoma
/ Metastases
/ Mutation
/ Neoantigens
/ Ovarian cancer
/ Patients
/ Peptides
/ Precision Medicine - methods
/ Protein Binding
/ Reagents
/ T-Cell Antigen Receptor Specificity
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ T-Lymphocytes - immunology
/ T-Lymphocytes - metabolism
/ Treatment Outcome
/ tumor-infiltrating lymphocyte (TIL)
2020
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Neoantigen-Specific Adoptive Cell Therapies for Cancer: Making T-Cell Products More Personal
by
Harari, Alexandre
, Bianchi, Valentina
, Coukos, George
in
adoptive cell therapy (ACT)
/ Animals
/ Antigens
/ Antigens, Neoplasm - immunology
/ Antitumor activity
/ Biomarkers
/ cancer immunotherapy
/ Cell therapy
/ Cells
/ Cells, Cultured
/ Clinical Studies as Topic
/ Coculture Techniques
/ Cytokines - metabolism
/ Cytomegalovirus
/ enrichment
/ Epitopes, T-Lymphocyte - immunology
/ HLA Antigens - immunology
/ Humans
/ Immune response
/ Immunology
/ Immunotherapy
/ Immunotherapy, Adoptive - methods
/ Lymphocyte Activation - immunology
/ Lymphocytes
/ Lymphocytes T
/ Lymphocytes, Tumor-Infiltrating - immunology
/ Lymphocytes, Tumor-Infiltrating - metabolism
/ Major histocompatibility complex
/ Melanoma
/ Metastases
/ Mutation
/ Neoantigens
/ Ovarian cancer
/ Patients
/ Peptides
/ Precision Medicine - methods
/ Protein Binding
/ Reagents
/ T-Cell Antigen Receptor Specificity
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ T-Lymphocytes - immunology
/ T-Lymphocytes - metabolism
/ Treatment Outcome
/ tumor-infiltrating lymphocyte (TIL)
2020
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Neoantigen-Specific Adoptive Cell Therapies for Cancer: Making T-Cell Products More Personal
by
Harari, Alexandre
, Bianchi, Valentina
, Coukos, George
in
adoptive cell therapy (ACT)
/ Animals
/ Antigens
/ Antigens, Neoplasm - immunology
/ Antitumor activity
/ Biomarkers
/ cancer immunotherapy
/ Cell therapy
/ Cells
/ Cells, Cultured
/ Clinical Studies as Topic
/ Coculture Techniques
/ Cytokines - metabolism
/ Cytomegalovirus
/ enrichment
/ Epitopes, T-Lymphocyte - immunology
/ HLA Antigens - immunology
/ Humans
/ Immune response
/ Immunology
/ Immunotherapy
/ Immunotherapy, Adoptive - methods
/ Lymphocyte Activation - immunology
/ Lymphocytes
/ Lymphocytes T
/ Lymphocytes, Tumor-Infiltrating - immunology
/ Lymphocytes, Tumor-Infiltrating - metabolism
/ Major histocompatibility complex
/ Melanoma
/ Metastases
/ Mutation
/ Neoantigens
/ Ovarian cancer
/ Patients
/ Peptides
/ Precision Medicine - methods
/ Protein Binding
/ Reagents
/ T-Cell Antigen Receptor Specificity
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ T-Lymphocytes - immunology
/ T-Lymphocytes - metabolism
/ Treatment Outcome
/ tumor-infiltrating lymphocyte (TIL)
2020
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Neoantigen-Specific Adoptive Cell Therapies for Cancer: Making T-Cell Products More Personal
Journal Article
Neoantigen-Specific Adoptive Cell Therapies for Cancer: Making T-Cell Products More Personal
2020
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Overview
Mutation-derived neoantigens are taking central stage as a determinant in eliciting effective antitumor immune responses following adoptive T-cell therapies. These mutations are patient-specific, and their targeting calls for highly personalized pipelines. The promising clinical outcomes of tumor-infiltrating lymphocyte (TIL) therapy have spurred interest in generating T-cell infusion products that have been selectively enriched in neoantigen (or autologous tumor) reactivity. The implementation of an isolation step, prior to T-cell
expansion and reinfusion, may provide a way to improve the overall response rates achieved to date by adoptive T-cell therapies in metastatic cancer patients. Here we provide an overview of the main technologies [i.e., peptide major histocompatibility complex (pMHC) multimers, cytokine capture, and activation markers] to enrich infiltrating or circulating T-cells in predefined neoantigen specificities (or tumor reactivity). The unique technical and regulatory challenges faced by such highly specialized and patient-specific manufacturing T-cell platforms are also discussed.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
/ Animals
/ Antigens
/ Antigens, Neoplasm - immunology
/ Cells
/ Epitopes, T-Lymphocyte - immunology
/ Humans
/ Immunotherapy, Adoptive - methods
/ Lymphocyte Activation - immunology
/ Lymphocytes, Tumor-Infiltrating - immunology
/ Lymphocytes, Tumor-Infiltrating - metabolism
/ Major histocompatibility complex
/ Melanoma
/ Mutation
/ Patients
/ Peptides
/ Precision Medicine - methods
/ Reagents
/ T-Cell Antigen Receptor Specificity
/ T-Lymphocyte Subsets - immunology
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