Nature Immunology, ISSN 1529-2908, 09/2019, Volume 20, Issue 9, pp. 1231 - 1243
Understanding resistance to antibody to programmed cell death protein 1 (PD-1; anti-PD-1) is crucial for the development of reversal strategies. In...
Antigens | Therapy | PD-1 protein | CD8 antigen | Antibodies | Reversing | Priming | T cell receptors | Lymphocytes T | Vaccines | Optimization | T-cell receptor | Cell death | Lymphocytes | CD38 antigen | Biomarkers | Tumors | Apoptosis
Antigens | Therapy | PD-1 protein | CD8 antigen | Antibodies | Reversing | Priming | T cell receptors | Lymphocytes T | Vaccines | Optimization | T-cell receptor | Cell death | Lymphocytes | CD38 antigen | Biomarkers | Tumors | Apoptosis
Journal Article
Nature Immunology, ISSN 1529-2908, 11/2019, Volume 20, Issue 11, pp. 1555 - 1555
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
PD-1 protein | CD8 antigen
PD-1 protein | CD8 antigen
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1136 - 11
Treatment with immune checkpoint blockade (CPB) therapies often leads to prolonged responses in patients with metastatic melanoma, but the common mechanisms of...
PLATFORM | METASTATIC MELANOMA | CTLA-4 BLOCKADE | PEMBROLIZUMAB | GENOMICS | PD-1 BLOCKADE | MULTIDISCIPLINARY SCIENCES | ACQUIRED-RESISTANCE | CANCER-IMMUNOTHERAPY | MUTATIONS | TUMORS | Humans | Mice, Inbred C57BL | Antibodies, Monoclonal - therapeutic use | Antigen Presentation - genetics | Melanoma - pathology | CTLA-4 Antigen - immunology | Loss of Heterozygosity | Mice, Knockout | Neoplasms, Experimental - pathology | Point Mutation | Drug Resistance, Neoplasm - genetics | Neoplasm Metastasis | Animals | Melanoma - genetics | Melanoma - drug therapy | Neoplasms, Experimental - genetics | Female | Antigen Presentation - drug effects | Programmed Cell Death 1 Receptor - immunology | Neoplasms, Experimental - drug therapy | Antibodies, Monoclonal - immunology | beta 2-Microglobulin - genetics | Drug Resistance, Neoplasm - drug effects | Antigen presentation | Deactivation | PD-1 protein | Melanoma | Metastasis | Inactivation | Patients | Metastases | Heterozygosity | CTLA-4 protein | Major histocompatibility complex | Immune checkpoint | Loss of heterozygosity | Mutation | Target acquisition
PLATFORM | METASTATIC MELANOMA | CTLA-4 BLOCKADE | PEMBROLIZUMAB | GENOMICS | PD-1 BLOCKADE | MULTIDISCIPLINARY SCIENCES | ACQUIRED-RESISTANCE | CANCER-IMMUNOTHERAPY | MUTATIONS | TUMORS | Humans | Mice, Inbred C57BL | Antibodies, Monoclonal - therapeutic use | Antigen Presentation - genetics | Melanoma - pathology | CTLA-4 Antigen - immunology | Loss of Heterozygosity | Mice, Knockout | Neoplasms, Experimental - pathology | Point Mutation | Drug Resistance, Neoplasm - genetics | Neoplasm Metastasis | Animals | Melanoma - genetics | Melanoma - drug therapy | Neoplasms, Experimental - genetics | Female | Antigen Presentation - drug effects | Programmed Cell Death 1 Receptor - immunology | Neoplasms, Experimental - drug therapy | Antibodies, Monoclonal - immunology | beta 2-Microglobulin - genetics | Drug Resistance, Neoplasm - drug effects | Antigen presentation | Deactivation | PD-1 protein | Melanoma | Metastasis | Inactivation | Patients | Metastases | Heterozygosity | CTLA-4 protein | Major histocompatibility complex | Immune checkpoint | Loss of heterozygosity | Mutation | Target acquisition
Journal Article
Nature immunology, 09/2019, Volume 20, Issue 9, p. 1231
Understanding resistance to antibody to programmed cell death protein 1 (PD-1; anti-PD-1) is crucial for the development of reversal strategies. In...
Journal Article
5.
Full Text
Defining T Cell States Associated with Response to Checkpoint Immunotherapy in Melanoma
Cell, ISSN 0092-8674, 11/2018, Volume 175, Issue 4, pp. 998 - 1013.e20
Treatment of cancer has been revolutionized by immune checkpoint blockade therapies. Despite the high rate of response in advanced melanoma, the majority of...
checkpoint blockade | CD8+ T cells | single-cell RNA-seq | cancer immunotherapy | TCF7 | T cells | CD8 | METASTATIC MELANOMA | CTLA-4 BLOCKADE | READ ALIGNMENT | RNA-SEQ | PD-1 BLOCKADE | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR-CELLS | CANCER-IMMUNOTHERAPY | CHRONIC VIRAL-INFECTION | ANTITUMOR-ACTIVITY | CLINICAL-RESPONSE | CELL BIOLOGY | Proteins | Care and treatment | RNA | Immunotherapy | Melanoma | Development and progression | Drug therapy | Cancer
checkpoint blockade | CD8+ T cells | single-cell RNA-seq | cancer immunotherapy | TCF7 | T cells | CD8 | METASTATIC MELANOMA | CTLA-4 BLOCKADE | READ ALIGNMENT | RNA-SEQ | PD-1 BLOCKADE | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR-CELLS | CANCER-IMMUNOTHERAPY | CHRONIC VIRAL-INFECTION | ANTITUMOR-ACTIVITY | CLINICAL-RESPONSE | CELL BIOLOGY | Proteins | Care and treatment | RNA | Immunotherapy | Melanoma | Development and progression | Drug therapy | Cancer
Journal Article
6.
Full Text
Defining T Cell States Associated with Response to Checkpoint Immunotherapy in Melanoma
Cell, ISSN 0092-8674, 01/2019, Volume 176, Issue 1-2, pp. 404 - 404
Journal Article
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