Publication: Humanized Mouse Models to Evaluate Cancer Immunotherapeutics
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Identifiers
Date
2021-01-01
Authors
Guil-Luna, Silvia
Sedlik, Christine
Piaggio, Eliane
Jacks, T
Sawyers, CL
Advisors
Journal Title
Journal ISSN
Volume Title
Publisher
Annual Reviews
Abstract
Immunotherapy is at the forefront of cancer treatment. The advent of numerous novel approaches to cancer immunotherapy, including immune checkpoint antibodies, adoptive transfer of CAR (chimeric antigen receptor) T cells and TCR (T cell receptor) T cells, NK (natural killer) cells, T cell engagers, oncolytic viruses, and vaccines, is revolutionizing the treatment for different tumor types. Some are already in the clinic, and many others are underway. However, not all patients respond, resistance develops, and as available therapies multiply there is a need to further understand how they work, how to prioritize their clinical evaluation, and how to combine them. For this, animal models have been highly instrumental, and humanized mice models (i.e., immunodeficient mice engrafted with human immune and cancer cells) represent a step forward, although they have several limitations. Here, we review the different humanized models available today, the approaches to overcome their flaws, their use for the evaluation of cancer immunotherapies, and their anticipated evolution as tools to help personalized clinical decision-making.
Description
MeSH Terms
T-cells
Immune-responses
Antitumor-activity
Class-i
Solid tumors
Gm-csf
Reconstitution
Generation
Induction
Immune-responses
Antitumor-activity
Class-i
Solid tumors
Gm-csf
Reconstitution
Generation
Induction
DeCS Terms
Factor estimulante de colonias de granulocitos y macrófagos
Linfocitos T
Neoplasias
Linfocitos T
Neoplasias
CIE Terms
Keywords
Humanized mice, Immuno-oncology, Preclinical research, Immunotherapy, Cancer, Patient-derived xenograft, Lymphoid-system mice
Citation
Guil-Luna S, Sedlik C, Piaggio E. Humanized Mouse Models to Evaluate Cancer Immunotherapeutics. Annual Review Of Cancer Biology [Internet]. 4 de marzo de 2021;5(1):119-36