Nature Biotechnology, ISSN 1087-0156, 07/2012, Volume 30, Issue 7, pp. 658 - 670
Oncolytic virotherapy is an emerging treatment modality that uses replication-competent viruses to destroy cancers. Recent advances include preclinical proof...
TUMOR-SPECIFIC DEFECTS | MEDIATED GENE-EXPRESSION | HERPES-SIMPLEX-VIRUS | INTRATUMORAL SPREAD | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | NONLINEAR DOSE-RESPONSE | MEASLES-VIRUS | VESICULAR STOMATITIS-VIRUS | PHASE-I | MESENCHYMAL STEM-CELLS | T-CELLS | Neoplasms - therapy | Humans | Simplexvirus - genetics | Adenoviridae - genetics | Oncolytic Viruses - genetics | Clinical Trials as Topic | Genetic Vectors | Immunity, Cellular | Oncolytic Virotherapy | Biotechnology | Oncology | Viruses | Propagation | Cancer therapies
TUMOR-SPECIFIC DEFECTS | MEDIATED GENE-EXPRESSION | HERPES-SIMPLEX-VIRUS | INTRATUMORAL SPREAD | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | NONLINEAR DOSE-RESPONSE | MEASLES-VIRUS | VESICULAR STOMATITIS-VIRUS | PHASE-I | MESENCHYMAL STEM-CELLS | T-CELLS | Neoplasms - therapy | Humans | Simplexvirus - genetics | Adenoviridae - genetics | Oncolytic Viruses - genetics | Clinical Trials as Topic | Genetic Vectors | Immunity, Cellular | Oncolytic Virotherapy | Biotechnology | Oncology | Viruses | Propagation | Cancer therapies
Journal Article
Journal of Vascular and Interventional Radiology, ISSN 1051-0443, 2013, Volume 24, Issue 8, pp. 1115 - 1122
Abstract Oncolytic virotherapy is an emerging technology that uses engineered viruses to treat malignancies. Viruses can be designed with biological...
Radiology | VIRUS NV1020 | JX-594 | I/II TRIAL | THERAPY | CLINICAL-TRIAL | PHASE-I TRIAL | INJECTION | PERIPHERAL VASCULAR DISEASE | REPLICATION-COMPETENT | CANCER | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | ADENOVIRUS ONYX-015 | Radiography, Interventional | History, 21st Century | History, 20th Century | Humans | Cytopathogenic Effect, Viral | Host Specificity | Oncolytic Viruses - genetics | Oncolytic Viruses - pathogenicity | Treatment Outcome | Neoplasms - history | Neoplasms - virology | Neoplasms - therapy | Animals | Oncolytic Virotherapy - history | Neoplasms - pathology | Oncolytic Virotherapy - adverse effects
Radiology | VIRUS NV1020 | JX-594 | I/II TRIAL | THERAPY | CLINICAL-TRIAL | PHASE-I TRIAL | INJECTION | PERIPHERAL VASCULAR DISEASE | REPLICATION-COMPETENT | CANCER | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | ADENOVIRUS ONYX-015 | Radiography, Interventional | History, 21st Century | History, 20th Century | Humans | Cytopathogenic Effect, Viral | Host Specificity | Oncolytic Viruses - genetics | Oncolytic Viruses - pathogenicity | Treatment Outcome | Neoplasms - history | Neoplasms - virology | Neoplasms - therapy | Animals | Oncolytic Virotherapy - history | Neoplasms - pathology | Oncolytic Virotherapy - adverse effects
Journal Article
2012
Source: National Library of New Zealand Te Puna Matauranga o Aotearoa, licensed by the Department of Internal Affairs for re-use under the Creative Commons...
Viruses | Treatment | Therapeutic use | Cancer
Viruses | Treatment | Therapeutic use | Cancer
eJournal
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2018, Volume 1045, pp. 63 - 84
Oncolytic virotherapy is a kind of antitumor therapy using viruses with natural or engineered tumor-selective replication to intentionally infect and kill...
G207 | HSV1716 | Talimogene laherparepvec | OncoVEX | Oncolytic virotherapy | NV1020 | HSV | HF10 | Herpes simplex virus | T-VEC | MEDICINE, RESEARCH & EXPERIMENTAL | TUMOR | INTRATUMORAL INJECTION | REPLICATION-COMPETENT | PHASE I/II | CANCER | OncoVEX(GM-CSF) | HERPES-SIMPLEX-VIRUS | VIROLOGY | DNA-SEQUENCE | VIRAL THERAPY | BIOLOGY | TYPE-1 MUTANT HF10 | Oncolytic Virotherapy - methods | Neoplasms - therapy | Animals | Oncolytic Virotherapy - trends | Simplexvirus - physiology | Humans | Simplexvirus - genetics | Oncolytic Viruses - physiology | Oncolytic Viruses - genetics
G207 | HSV1716 | Talimogene laherparepvec | OncoVEX | Oncolytic virotherapy | NV1020 | HSV | HF10 | Herpes simplex virus | T-VEC | MEDICINE, RESEARCH & EXPERIMENTAL | TUMOR | INTRATUMORAL INJECTION | REPLICATION-COMPETENT | PHASE I/II | CANCER | OncoVEX(GM-CSF) | HERPES-SIMPLEX-VIRUS | VIROLOGY | DNA-SEQUENCE | VIRAL THERAPY | BIOLOGY | TYPE-1 MUTANT HF10 | Oncolytic Virotherapy - methods | Neoplasms - therapy | Animals | Oncolytic Virotherapy - trends | Simplexvirus - physiology | Humans | Simplexvirus - genetics | Oncolytic Viruses - physiology | Oncolytic Viruses - genetics
Journal Article
Archives of disease in childhood - Education & practice edition, ISSN 1743-0585, 02/2018, Volume 103, Issue 1, pp. 43 - 45
oncolytic virotherapy | PEDIATRICS | paediatric practice | IMMUNOTHERAPY | oncolytic virus | VIRUSES | Humans | Child, Preschool | Infant | Male | Oncolytic Viruses - pathogenicity | Neoplasms - virology | Oncolytic Virotherapy - methods | Neoplasms - therapy | Pediatrics - methods | Adolescent | Female | Child | Infant, Newborn
Journal Article
Expert Opinion on Biological Therapy, ISSN 1471-2598, 06/2019, Volume 19, Issue 6, pp. 561 - 573
Introduction: Over the last decade, advances in biological therapies have resulted in remarkable clinical responses for the treatment of some previously...
Vaccinia virus | Myxoma virus | oncolytic | virotherapy | oncolytic virus | MULTIPLE-MYELOMA | MEDICINE, RESEARCH & EXPERIMENTAL | SAFETY | IMMUNOTHERAPEUTIC VACCINIA VIRUS | IMMUNOCOMPETENT MOUSE MODEL | TUMOR-INITIATING CELLS | IN-VITRO | THERAPY | PEXA-VEC JX-594 | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | XENOGRAFT MODEL
Vaccinia virus | Myxoma virus | oncolytic | virotherapy | oncolytic virus | MULTIPLE-MYELOMA | MEDICINE, RESEARCH & EXPERIMENTAL | SAFETY | IMMUNOTHERAPEUTIC VACCINIA VIRUS | IMMUNOCOMPETENT MOUSE MODEL | TUMOR-INITIATING CELLS | IN-VITRO | THERAPY | PEXA-VEC JX-594 | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | XENOGRAFT MODEL
Journal Article
Cancer, ISSN 0008-543X, 11/2014, Volume 120, Issue 21, pp. 3277 - 3286
Recently, the century‐old idea of targeting cancer with viruses (oncolytic viruses) has come of age, and promise has been documented in early stage and several...
innate antiviral response | eIF4G | oncolytic virus | nectin‐like molecule 5 | translation | interferon | internal ribosomal entry site | poliovirus | CD155 | nectin-like molecule 5 | VIRUS | CELL-MOVEMENT | FACTOR 4G1 EIF4G1 | TRANSLATION INITIATION | SIGNAL-TRANSDUCTION | MALIGNANT GLIOMA | HELICASE COMPLEX | MESSENGER-RNA | ONCOLOGY | RIBOSOME ENTRY SITE | BINDING | Neoplasms - virology | Neoplasms - therapy | Neoplasms - genetics | Humans | Immunotherapy | Immunity, Innate - genetics | Receptors, Virus - immunology | Oncolytic Viruses - genetics | Poliomyelitis - genetics | Oncolytic Virotherapy | Virus Internalization | IRES | Necl5
innate antiviral response | eIF4G | oncolytic virus | nectin‐like molecule 5 | translation | interferon | internal ribosomal entry site | poliovirus | CD155 | nectin-like molecule 5 | VIRUS | CELL-MOVEMENT | FACTOR 4G1 EIF4G1 | TRANSLATION INITIATION | SIGNAL-TRANSDUCTION | MALIGNANT GLIOMA | HELICASE COMPLEX | MESSENGER-RNA | ONCOLOGY | RIBOSOME ENTRY SITE | BINDING | Neoplasms - virology | Neoplasms - therapy | Neoplasms - genetics | Humans | Immunotherapy | Immunity, Innate - genetics | Receptors, Virus - immunology | Oncolytic Viruses - genetics | Poliomyelitis - genetics | Oncolytic Virotherapy | Virus Internalization | IRES | Necl5
Journal Article
Cell, ISSN 0092-8674, 09/2017, Volume 170, Issue 6, pp. 1109 - 1119.e10
Here we report a phase 1b clinical trial testing the impact of oncolytic virotherapy with talimogene laherparepvec on cytotoxic T cell infiltration and...
T lymphocytes | pembrolizumab | interferon gamma | talimogene laherparepvec | biomarkers | tumor | oncolytic immunotherapy | melanoma | cytotixic | tumor microenvironment | oncolytic viruses | anti-PD-1 | PEMBROLIZUMAB | THERAPY | ADVANCED MELANOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ADAPTIVE IMMUNE RESISTANCE | ANTIBODY | BLOCKADE | CANCER | TALIMOGENE LAHERPAREPVEC | IPILIMUMAB | CELL BIOLOGY | Antibodies, Monoclonal, Humanized - administration & dosage | Humans | Immunotherapy | Herpesviridae - genetics | Tumor Microenvironment | Programmed Cell Death 1 Receptor - antagonists & inhibitors | Combined Modality Therapy | Melanoma - therapy | Oncolytic Virotherapy - adverse effects | Melanoma | Metastasis | Biological response modifiers | T cells | Gene expression | Health aspects | Interferon gamma
T lymphocytes | pembrolizumab | interferon gamma | talimogene laherparepvec | biomarkers | tumor | oncolytic immunotherapy | melanoma | cytotixic | tumor microenvironment | oncolytic viruses | anti-PD-1 | PEMBROLIZUMAB | THERAPY | ADVANCED MELANOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ADAPTIVE IMMUNE RESISTANCE | ANTIBODY | BLOCKADE | CANCER | TALIMOGENE LAHERPAREPVEC | IPILIMUMAB | CELL BIOLOGY | Antibodies, Monoclonal, Humanized - administration & dosage | Humans | Immunotherapy | Herpesviridae - genetics | Tumor Microenvironment | Programmed Cell Death 1 Receptor - antagonists & inhibitors | Combined Modality Therapy | Melanoma - therapy | Oncolytic Virotherapy - adverse effects | Melanoma | Metastasis | Biological response modifiers | T cells | Gene expression | Health aspects | Interferon gamma
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2018, Volume 36, Issue 14, pp. 1440 - 1442
Journal Article
Mayo Clinic Proceedings, ISSN 0025-6196, 2014, Volume 89, Issue 7, pp. 926 - 933
Abstract MV-NIS is an engineered measles virus that is selectively destructive to myeloma plasma cells and can be monitored by noninvasive radioiodine imaging...
Internal Medicine | MULTIPLE-MYELOMA | ANTIBODIES | CELLS | IMMUNITY | MEDICINE, GENERAL & INTERNAL | CYCLOPHOSPHAMIDE | POXVIRUS | MEASLES-VIRUS | INDUCTION | CARRIERS | DELIVERY | Multiple Myeloma - diagnostic imaging | Oncolytic Virotherapy - methods | Multiple Myeloma - therapy | Humans | Middle Aged | Radionuclide Imaging | Female | Aged | Infusions, Intravenous | Oncolytic Viruses | Measles virus | Melanoma | Genetic aspects | Dosage and administration | Research | Gene expression | Drug therapy | Health aspects | Isotopes | Oncogenic viruses | Iodine
Internal Medicine | MULTIPLE-MYELOMA | ANTIBODIES | CELLS | IMMUNITY | MEDICINE, GENERAL & INTERNAL | CYCLOPHOSPHAMIDE | POXVIRUS | MEASLES-VIRUS | INDUCTION | CARRIERS | DELIVERY | Multiple Myeloma - diagnostic imaging | Oncolytic Virotherapy - methods | Multiple Myeloma - therapy | Humans | Middle Aged | Radionuclide Imaging | Female | Aged | Infusions, Intravenous | Oncolytic Viruses | Measles virus | Melanoma | Genetic aspects | Dosage and administration | Research | Gene expression | Drug therapy | Health aspects | Isotopes | Oncogenic viruses | Iodine
Journal Article
Science Translational Medicine, ISSN 1946-6234, 01/2018, Volume 10, Issue 422, p. eaao1641
Triple-negative breast cancer (TNBC) is an aggressive disease for which treatment options are limited and associated with severe toxicities. Immunotherapeutic...
MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | JX-594 | VIRUS | IMMUNOTHERAPY | VEC | DISEASE | OUTCOMES | CARCINOMA | CELL BIOLOGY | Oncolytic Virotherapy - methods | Female | Humans | Neoadjuvant Therapy - methods | Triple Negative Breast Neoplasms - therapy | Oncolytic Viruses - physiology
MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | JX-594 | VIRUS | IMMUNOTHERAPY | VEC | DISEASE | OUTCOMES | CARCINOMA | CELL BIOLOGY | Oncolytic Virotherapy - methods | Female | Humans | Neoadjuvant Therapy - methods | Triple Negative Breast Neoplasms - therapy | Oncolytic Viruses - physiology
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12.
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TGFβ treatment enhances glioblastoma virotherapy by inhibiting the innate immune response
Cancer Research, ISSN 0008-5472, 12/2015, Volume 75, Issue 24, pp. 5273 - 5282
Oncolytic viruses, including oncolytic herpes simplex virus (oHSV), have produced provocative therapeutic responses in patients with glioblastoma, the most...
GROWTH-FACTOR-BETA | NKG2D | ONCOLYTIC VIRUS THERAPY | NK CELLS | ONCOLOGY | INDUCTION | TUMORS | BRAIN | Immunity, Innate - drug effects | Humans | Reverse Transcriptase Polymerase Chain Reaction | Xenograft Model Antitumor Assays | Oncolytic Virotherapy - methods | Transforming Growth Factor beta - pharmacology | Simplexvirus | Animals | Brain Neoplasms - immunology | Flow Cytometry | Glioblastoma - immunology | Mice, Inbred NOD | Mice | Oncolytic Viruses | Immunosuppressive Agents - pharmacology | Real-Time Polymerase Chain Reaction | Disease Models, Animal | TGF-β | NK cells | glioblastoma | Oncolytic Herpes Simplex Virus | oncolytic viruses | innate immune response
GROWTH-FACTOR-BETA | NKG2D | ONCOLYTIC VIRUS THERAPY | NK CELLS | ONCOLOGY | INDUCTION | TUMORS | BRAIN | Immunity, Innate - drug effects | Humans | Reverse Transcriptase Polymerase Chain Reaction | Xenograft Model Antitumor Assays | Oncolytic Virotherapy - methods | Transforming Growth Factor beta - pharmacology | Simplexvirus | Animals | Brain Neoplasms - immunology | Flow Cytometry | Glioblastoma - immunology | Mice, Inbred NOD | Mice | Oncolytic Viruses | Immunosuppressive Agents - pharmacology | Real-Time Polymerase Chain Reaction | Disease Models, Animal | TGF-β | NK cells | glioblastoma | Oncolytic Herpes Simplex Virus | oncolytic viruses | innate immune response
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 10/2018, Volume 837, pp. 117 - 126
Oncolytic viruses are a fast-developing cancer treatment field. Numerous viruses have been tested in clinical trials and three are approved. The first, Rigvir,...
Rigvir | Oncolytic | ECHO-7 virus | Oncotropism | Melanoma | Virotherapy | NEWCASTLE-DISEASE-VIRUS | ECHOVIRUS INFECTION | ROSETTE FORMATION | FACTOR CD55 | CONTINUING SURVEILLANCE | CANCER-TREATMENT | HISTIOCYTIC SARCOMA | DECAY-ACCELERATING FACTOR | RHABDOMYOSARCOMA CELLS | PHARMACOLOGY & PHARMACY | Oncolytic Virotherapy - methods | Animals | Humans | Enterovirus B, Human | Clinical Trials as Topic | Drug Evaluation, Preclinical | Melanoma - therapy | Oncolytic Virotherapy - adverse effects | Immunologic Factors - therapeutic use | Melanoma - mortality | Oncology, Experimental | Mortality | Colorectal cancer | Development and progression | Metastasis | Research | Prevention | Analysis | Immunotherapy | Skin care products | Health aspects | Cancer
Rigvir | Oncolytic | ECHO-7 virus | Oncotropism | Melanoma | Virotherapy | NEWCASTLE-DISEASE-VIRUS | ECHOVIRUS INFECTION | ROSETTE FORMATION | FACTOR CD55 | CONTINUING SURVEILLANCE | CANCER-TREATMENT | HISTIOCYTIC SARCOMA | DECAY-ACCELERATING FACTOR | RHABDOMYOSARCOMA CELLS | PHARMACOLOGY & PHARMACY | Oncolytic Virotherapy - methods | Animals | Humans | Enterovirus B, Human | Clinical Trials as Topic | Drug Evaluation, Preclinical | Melanoma - therapy | Oncolytic Virotherapy - adverse effects | Immunologic Factors - therapeutic use | Melanoma - mortality | Oncology, Experimental | Mortality | Colorectal cancer | Development and progression | Metastasis | Research | Prevention | Analysis | Immunotherapy | Skin care products | Health aspects | Cancer
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Defining effective combinations of immune checkpoint blockade and oncolytic virotherapy
Clinical Cancer Research, ISSN 1078-0432, 12/2015, Volume 21, Issue 24, pp. 5543 - 5551
Purpose: Recent data from randomized clinical trials with oncolytic viral therapies and with cancer immunotherapies have finally recapitulated the promise...
INTERFERON | THERAPY | PROTEIN | ONCOLOGY | SAFETY | POXVIRUS | TUMOR | ANTIBODY | VACCINIA VIRUS | CANCER-IMMUNOTHERAPY | CELL | Neoplasms - metabolism | T-Lymphocyte Subsets - immunology | Immunomodulation - drug effects | Immunotherapy - methods | Interleukin-2 Receptor alpha Subunit - antagonists & inhibitors | Programmed Cell Death 1 Receptor - antagonists & inhibitors | Neoplasms - diagnosis | Molecular Targeted Therapy | Vaccinia virus - drug effects | Vaccinia virus - genetics | Neoplasms - therapy | Female | Antineoplastic Agents - pharmacology | Disease Models, Animal | Virus Replication - drug effects | Antibodies, Monoclonal - pharmacology | Oncolytic Viruses - genetics | Combined Modality Therapy | Genetic Vectors - genetics | Oncolytic Virotherapy - methods | Animals | B7-H1 Antigen - antagonists & inhibitors | Tumor Burden - drug effects | Neoplasms - immunology | T-Lymphocyte Subsets - metabolism | Cell Line, Tumor | Mice | CTLA-4 Antigen - antagonists & inhibitors | Immunity, Cellular | CTLA4 | Vaccinia | Oncolytic Virus | immunotherapy | checkpoint inhibitor
INTERFERON | THERAPY | PROTEIN | ONCOLOGY | SAFETY | POXVIRUS | TUMOR | ANTIBODY | VACCINIA VIRUS | CANCER-IMMUNOTHERAPY | CELL | Neoplasms - metabolism | T-Lymphocyte Subsets - immunology | Immunomodulation - drug effects | Immunotherapy - methods | Interleukin-2 Receptor alpha Subunit - antagonists & inhibitors | Programmed Cell Death 1 Receptor - antagonists & inhibitors | Neoplasms - diagnosis | Molecular Targeted Therapy | Vaccinia virus - drug effects | Vaccinia virus - genetics | Neoplasms - therapy | Female | Antineoplastic Agents - pharmacology | Disease Models, Animal | Virus Replication - drug effects | Antibodies, Monoclonal - pharmacology | Oncolytic Viruses - genetics | Combined Modality Therapy | Genetic Vectors - genetics | Oncolytic Virotherapy - methods | Animals | B7-H1 Antigen - antagonists & inhibitors | Tumor Burden - drug effects | Neoplasms - immunology | T-Lymphocyte Subsets - metabolism | Cell Line, Tumor | Mice | CTLA-4 Antigen - antagonists & inhibitors | Immunity, Cellular | CTLA4 | Vaccinia | Oncolytic Virus | immunotherapy | checkpoint inhibitor
Journal Article
Molecular Therapy, ISSN 1525-0016, 05/2017, Volume 25, Issue 5, pp. 1107 - 1116
Viruses can be engineered or adapted for selective propagation in neoplastic tissues and further modified for therapeutic transgene expression to enhance their...
competitive landscape | oncolytic virotherapy | viro-immuno-oncology | T-VEC | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICAL-TRIAL | MEASLES VIRUSES | INTRAVENOUS DELIVERY | OVARIAN-CANCER | CANCER-THERAPY | HERPES-SIMPLEX-VIRUS | LAHERPAREPVEC T-VEC | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | VESICULAR STOMATITIS-VIRUS | TALIMOGENE LAHERPAREPVEC | ANTITUMOR EFFICACY | Lymph Nodes - pathology | Humans | Mutant Chimeric Proteins - genetics | Plasmacytoma - genetics | Multiple Myeloma - immunology | Plasmacytoma - immunology | Plasmacytoma - pathology | Measles virus - genetics | Multiple Myeloma - therapy | Antigen Presentation | Melanoma - genetics | Mutant Chimeric Proteins - metabolism | T-Lymphocytes - pathology | Skin Neoplasms - pathology | Antigens, Neoplasm - genetics | Oncolytic Virotherapy - trends | Genetic Vectors - chemistry | Herpesvirus 1, Human - metabolism | Skin Neoplasms - immunology | Skin Neoplasms - therapy | Antigens, Neoplasm - immunology | Genetic Vectors - metabolism | Oncolytic Viruses - genetics | Lymph Nodes - immunology | Melanoma - pathology | Oncolytic Virotherapy - methods | Multiple Myeloma - pathology | Measles virus - metabolism | Melanoma - immunology | Oncolytic Viruses - immunology | Plasmacytoma - therapy | Skin Neoplasms - genetics | Herpesvirus 1, Human - genetics | T-Lymphocytes - immunology | Melanoma - therapy | Multiple Myeloma - genetics | Tumor cells | Immunomodulation | Melanoma | Antibodies | Viruses | Lymphocytes T | Kinases | Macrophages | Lymph nodes | Skin cancer | Metastases | Immune checkpoint | Immunotherapy | Antigen (tumor-associated) | Oncolysis | Review
competitive landscape | oncolytic virotherapy | viro-immuno-oncology | T-VEC | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICAL-TRIAL | MEASLES VIRUSES | INTRAVENOUS DELIVERY | OVARIAN-CANCER | CANCER-THERAPY | HERPES-SIMPLEX-VIRUS | LAHERPAREPVEC T-VEC | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | VESICULAR STOMATITIS-VIRUS | TALIMOGENE LAHERPAREPVEC | ANTITUMOR EFFICACY | Lymph Nodes - pathology | Humans | Mutant Chimeric Proteins - genetics | Plasmacytoma - genetics | Multiple Myeloma - immunology | Plasmacytoma - immunology | Plasmacytoma - pathology | Measles virus - genetics | Multiple Myeloma - therapy | Antigen Presentation | Melanoma - genetics | Mutant Chimeric Proteins - metabolism | T-Lymphocytes - pathology | Skin Neoplasms - pathology | Antigens, Neoplasm - genetics | Oncolytic Virotherapy - trends | Genetic Vectors - chemistry | Herpesvirus 1, Human - metabolism | Skin Neoplasms - immunology | Skin Neoplasms - therapy | Antigens, Neoplasm - immunology | Genetic Vectors - metabolism | Oncolytic Viruses - genetics | Lymph Nodes - immunology | Melanoma - pathology | Oncolytic Virotherapy - methods | Multiple Myeloma - pathology | Measles virus - metabolism | Melanoma - immunology | Oncolytic Viruses - immunology | Plasmacytoma - therapy | Skin Neoplasms - genetics | Herpesvirus 1, Human - genetics | T-Lymphocytes - immunology | Melanoma - therapy | Multiple Myeloma - genetics | Tumor cells | Immunomodulation | Melanoma | Antibodies | Viruses | Lymphocytes T | Kinases | Macrophages | Lymph nodes | Skin cancer | Metastases | Immune checkpoint | Immunotherapy | Antigen (tumor-associated) | Oncolysis | Review
Journal Article