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Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. SY18-02 - SY18-02
Journal Article
Nature, ISSN 0028-0836, 07/2015, Volume 523, Issue 7559, pp. 231 - 235
Journal Article
Immunity, ISSN 1074-7613, 07/2018, Volume 49, Issue 1, pp. 11 - 13
Pancreatic adenocarcinoma (PDAC) is mostly refractory to immunotherapies. In this issue of , generate a library of clonal PDAC tumors to examine the... 
IMMUNOLOGY | Career development | T cells | Pancreatic cancer | Immunotherapy | Adenocarcinoma | Antigens | Immune response | Dendritic cells | Lung cancer | Cloning | Melanoma | T cell receptors | Lymphocytes T | Metastasis | Immunity | Metastases | Ovarian cancer | Genotype & phenotype | Lymphocytes | Medical prognosis | Epigenetics | Infiltration | Pancreas | Chemokines | Tumors | Immune system
Journal Article
Journal for ImmunoTherapy of Cancer, ISSN 2051-1426, 2013, Volume 1, Issue 1, p. 16
An effective anti-tumor immune response requires the coordinated action of the innate and adaptive phases of the immune system. Critical processes include the... 
Denileukin diftitox | Tumor-associated antigen | Immunotherapy | Regulatory T cell | PD-L1 | CTLA-4 | Interferon | Indoleamine-2 | PD-1 | 3,-dioxygenase | Cancer | Antigens | Care and treatment | Immune response | Dendritic cells | Biological markers
Journal Article
Journal for ImmunoTherapy of Cancer, ISSN 2051-1426, 09/2015, Volume 3, Issue 1, p. 43
Increasing evidence is emerging that immunotherapeutic interventions, including checkpoint blockade, are predominantly effective in patients with a... 
Checkpoint inhibition | T-cell infiltration | Immune evasion | Tumor microenvironment | METASTASIS | IMMUNOLOGY | NEGATIVE BREAST-CANCER | MELANOMA | ONCOLOGY | MICE | BLOCKADE | EXPRESSION | PD-1 | Antigens | Medical research | Melanoma | T cell receptors | Genomes | Gene expression | Skin cancer | Studies | Genotype & phenotype | Lymphocytes | Immunotherapy | Ligands | Tumors
Journal Article
Cancer Cell, ISSN 1535-6108, 05/2017, Volume 31, Issue 5, pp. 711 - 723.e4
Effector T cells have the capability of recognizing and killing cancer cells. However, whether tumors can become immune resistant through exclusion of effector... 
T cell-inflamed tumor microenvironment | non-T cell-inflamed tumor microenvironment | immunotherapy resistance | immune escape | adoptive T cell transfer | METASTATIC MELANOMA | RESPONSES | IMMUNITY | MECHANISM | ONCOLOGY | CANCER REGRESSION | REJECTION | ANTIGENS | MICE | BLOCKADE | EXPRESSION | CELL BIOLOGY | Chemotaxis, Leukocyte | Tumor Escape | Basic-Leucine Zipper Transcription Factors - metabolism | Cell Proliferation | Dendritic Cells - immunology | Tumor Microenvironment | T-Lymphocytes - transplantation | Antigens, CD - metabolism | Repressor Proteins - deficiency | T-Lymphocytes - metabolism | Time Factors | Basic-Leucine Zipper Transcription Factors - deficiency | CD8-Positive T-Lymphocytes - metabolism | Dendritic Cells - metabolism | Repressor Proteins - metabolism | Melanoma - metabolism | Skin Neoplasms - pathology | Immunotherapy, Adoptive - methods | Signal Transduction | Skin Neoplasms - immunology | Skin Neoplasms - therapy | Repressor Proteins - genetics | Genotype | Integrin alpha Chains - metabolism | Basic-Leucine Zipper Transcription Factors - genetics | Melanoma - pathology | Tumor Burden | beta Catenin - metabolism | Mice, Knockout | Skin Neoplasms - metabolism | Phenotype | Animals | Melanoma - immunology | Chemokine CXCL9 - metabolism | Cell Line, Tumor | Immunologic Memory | T-Lymphocytes - immunology | CD8-Positive T-Lymphocytes - immunology | Melanoma - therapy | Chemokine CXCL10 - metabolism | Dendritic cells | T cells | Cancer | Immunotherapy | Adoptive T cell transfer
Journal Article