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Updated: Jan 24, 2026

Establishment of a Human Multiple Myeloma Xenograft Model in the Chicken to Study Tumor Growth, Invasion and Angiogenesis
Published on: May 1, 2015
Immunotherapeutics in Multiple Myeloma: How Can Translational Mouse Models Help?
Rachel E Cooke1,2, Rachel Koldej1,2, David Ritchie1,2
1Australian Cancer Research Foundation (ACRF) Translational Laboratory, Royal Melbourne Hospital, Melbourne, Australia.
Abstract:
Multiple myeloma (MM) is usually diagnosed in older adults at the time of immunosenescence, a collection of age-related changes in the immune system that contribute to increased susceptibility to infection and cancer. The MM tumor microenvironment and cumulative chemotherapies also add to defects in immunity over the course of disease. In this review we discuss how mouse models have furthered our understanding of the immune defects caused by MM and enabled immunotherapeutics to progress to clinical trials, but also question the validity of using immunodeficient models for these purposes. Immunocompetent models, in particular the 5T series and Vk⁎MYC models, are increasingly being utilized in preclinical studies and are adding to our knowledge of not only the adaptive immune system but also how the innate system might be enhanced in anti-MM activity. Finally we discuss the concept of immune profiling to target patients who might benefit the most from immunotherapeutics, and the use of humanized mice and 3D culture systems for personalized medicine.
Insights
Mouse models are crucial for understanding multiple myeloma (MM) and developing immunotherapies. Immunocompetent models offer new insights into innate and adaptive immunity for MM treatment.
Area of Science:
- Immunology
- Oncology
- Preclinical Research
Background:
- Multiple myeloma (MM) often affects older adults, coinciding with immunosenescence, increasing infection and cancer risk.
- The MM tumor microenvironment and chemotherapy exacerbate immune system defects during disease progression.
- Understanding MM-induced immune dysfunction is critical for effective treatment strategies.
Purpose of the Study:
- To review the role of mouse models in advancing MM research and immunotherapy development.
- To evaluate the utility of immunodeficient versus immunocompetent models for MM studies.
- To explore personalized medicine approaches for MM treatment.
Main Methods:
- Review of existing literature on mouse models in multiple myeloma research.
- Analysis of immunocompetent models (e.g., 5T series, Vk*MYC) for MM studies.
- Discussion of immune profiling, humanized mice, and 3D culture systems.
Main Results:
- Mouse models have significantly contributed to understanding MM-related immune defects and advancing immunotherapeutics.
- Immunocompetent models provide valuable insights into both adaptive and innate immune responses against MM.
- Immunodeficient models may have limitations in fully recapitulating MM's immune landscape.
Conclusions:
- Immunocompetent mouse models are increasingly important for preclinical MM research.
- Immune profiling and advanced models (humanized mice, 3D cultures) hold promise for personalized MM medicine.
- Further research using appropriate models is essential for optimizing MM immunotherapies.
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