Publication:
Humanized Mouse Models to Evaluate Cancer Immunotherapeutics

dc.contributor.authorGuil-Luna, Silvia
dc.contributor.authorSedlik, Christine
dc.contributor.authorPiaggio, Eliane
dc.contributor.authorJacks, T
dc.contributor.authorSawyers, CL
dc.contributor.authoraffiliation[Guil-Luna, Silvia] Maimonides Inst Biomed Res Cordoba IMIBIC, Cordoba 14004, Spain
dc.contributor.authoraffiliation[Sedlik, Christine] PSL Res Univ, Inst Curie, Res Ctr, Translat Res Dept,INSERM,U932, F-75248 Paris, France
dc.contributor.authoraffiliation[Piaggio, Eliane] PSL Res Univ, Inst Curie, Res Ctr, Translat Res Dept,INSERM,U932, F-75248 Paris, France
dc.contributor.funderSiRIC-Curie Program
dc.contributor.funderLabEx DCBIOL
dc.contributor.funderCenter of Clinical Investigation (CIC IGR-Curie )
dc.contributor.funderConsejeria de Salud de la Junta de Andalusia
dc.contributor.funderConsejería de Salud de la Junta de Andalusia
dc.date.accessioned2023-02-12T02:21:47Z
dc.date.available2023-02-12T02:21:47Z
dc.date.issued2021-01-01
dc.description.abstractImmunotherapy 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.
dc.description.sponsorshipThe TransImm team is supported by the SiRIC-Curie Program (grant INCa-DGOS-12554), the LabEx DCBIOL (ANR-10-IDEX-0001-02 PSL and ANR-11-LABX-0043), and the Center of Clinical Investigation (CIC IGR-Curie 1428). This work was partially supported by funding from “Consejería de Salud de la Junta de Andalusia” through the project PI-0150-2017.
dc.identifier.citationGuil-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
dc.identifier.doi10.1146/annurev-cancerbio-050520-100526
dc.identifier.issn2472-3428
dc.identifier.urihttp://hdl.handle.net/10668/19041
dc.identifier.wosID627716400007
dc.journal.titleAnnual review of cancer biology, vol 5, 2021
dc.journal.titleabbreviationAnnu. rev. canc. biol.
dc.language.isoen
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.page.number119-136
dc.publisherAnnual Reviews
dc.relation.ispartofseriesAnnual Review of Cancer Biology-Series
dc.relation.projectIDPI-0150-2017
dc.relation.publisherversionhttps://www.annualreviews.org/content/journals/10.1146/annurev-cancerbio-050520-100526
dc.subjectHumanized mice
dc.subjectImmuno-oncology
dc.subjectPreclinical research
dc.subjectImmunotherapy
dc.subject Cancer
dc.subjectPatient-derived xenograft
dc.subjectLymphoid-system mice
dc.subject.decsFactor estimulante de colonias de granulocitos y macrófagos
dc.subject.decsLinfocitos T
dc.subject.decsNeoplasias
dc.subject.meshT-cells
dc.subject.meshImmune-responses
dc.subject.meshAntitumor-activity
dc.subject.meshClass-i
dc.subject.meshSolid tumors
dc.subject.meshGm-csf
dc.subject.meshReconstitution
dc.subject.meshGeneration
dc.subject.meshInduction
dc.titleHumanized Mouse Models to Evaluate Cancer Immunotherapeutics
dc.typeresearch article
dc.typebook part
dc.volume.number5
dc.wostypeArticle
dc.wostypeBook Chapter
dspace.entity.typePublication

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