Reprint

Tumor Immunology and Immunotherapy Resistance

Edited by
September 2023
246 pages
  • ISBN978-3-0365-8702-8 (Hardback)
  • ISBN978-3-0365-8703-5 (PDF)

This book is a reprint of the Special Issue Tumor Immunology and Immunotherapy Resistance that was published in

Biology & Life Sciences
Medicine & Pharmacology
Summary

In recent years, cancer immunotherapy has made remarkable progress, revolutionizing cancer treatment. Our Special Issue "Cancer Immunology" in the journal Cancers showcased cutting-edge research and reviews. Building on that success, this new Special Issue explores recent advancements, technologies, and future prospects in cancer immunology, pre-clinical assessments, and clinical trials. While immune checkpoint inhibitors have been transformative, addressing limited response remains crucial. Strategies to overcome resistance, such as combination therapies and targeted pathways, are discussed in the issue. Chimeric antigen receptor (CAR) T cell therapy is an important area of immunotherapy, with exciting findings for enhancing CAR persistence and efficacy. Conventional treatments and monoclonal antibodies also activate immunological mechanisms, boosting cytotoxic efficacy against specific cancers. Identifying biomarkers associated with treatment response is vital for personalized cancer immunotherapy. Potential biomarkers like immune cell densities and estrogen receptor expression are explored in this Issue. The review articles cover advancements in CAR T cell therapy, tumor metabolic alterations, immune suppressive cells, and the role of bacteria in cancer immunotherapy. This Special Issue is a valuable resource for researchers, clinicians, and industry professionals, guiding future developments towards more effective and personalized cancer immunotherapies.

Format
  • Hardback
License and Copyright
© 2022 by the authors; CC BY-NC-ND license
Keywords
chimeric antigen receptor-T cells; neuroendocrine neoplasm; neuroendocrine tumor; neuroendocrine carcinoma; carcinoid tumor; somatostatin receptors; programmed death-ligand 1; cyclooxygenase-2; tumour resistance; immunosuppression; neuroblastoma; immunotherapy; dinutuximab beta; fibroblast activation protein α; FAP-IL-2v; myeloid-derived suppressor cells; tumor therapy; engineered bacteria; bacteria-based cancer treatment; microbiome; micronutrients; immunotherapy; cancer; pancreatic adenocarcinoma; estrogen receptor; tertiary lymphoid structure; tumor microenvironment; ADCC; carboplatin; chemoimmunotherapy; cisplatin; cyclophosphamide; dinutuximab beta; etoposide; neuroblastoma; vincristine; immunotherapy; chemotherapy; CSF1R; tumor-associated macrophages; myeloid-derived suppressor cells; trogocytosis; epidermal growth factor receptor variant III; chimeric antigen receptor T cells; autophagy; phagocytosis; glioblastoma; computational pathology; digital pathology; artificial intelligence; tumor-infiltrating lymphocytes; anti-tumor immune response; tumor microenvironment; predictive model; immunotherapy; Hodgkin’s lymphoma; nivolumab; ibrutinib; glioblastoma; immunotherapy; metabolism; tumor microenvironment; glycolysis; glutamine metabolism; lipid metabolism; tryptophan metabolism; PDOTS; ovarian cancer; ascites; epigenetic; methylation; ICB; PD-L1; PD-1; n/a

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