New mouse model technology in Melanoma vaccine tool-box
Mar 28, 2006 - 7:44:00 PM
, Reviewed by: Priya Saxena
|
|
The models we use to investigate cancer vaccines at the preclinical level either have a defined cancer antigen in a transplanted tumor, or they have an original tumor that doesnt have a defined antigen. However, in human clinical studies, we have original tumors with defined antigens. So there has been a need for a mouse model that more closely follows the human model.
|
By Ludwig Institute for Cancer Research,
[RxPG] Cancer vaccines are being investigated in early-phase clinical trials around the world, with many of those trials recruiting patients with melanoma. Although tumor regressions have been seen in 10% to 20% of patients with metastatic melanoma, the great promise of cancer vaccines - controlling tumor growth and cancer spread without serious side-effects - remains as yet unrealized. This could be set to change with the publication of a new mouse model technology in Cancer Research, the journal of the American Association of Cancer Research, from a multi-national team led by investigators at the Brussels Branch of the international Ludwig Institute for Cancer Research (LICR).
Melanoma has been a focus of cancer vaccine development because many melanoma-specific vaccine targets, so-called cancer antigens, have been defined, says the studys senior author, LICRs Dr. Benoit Van den Eynde. However, we have a limited understanding of how most, but not all, melanomas evade an immune system that has been primed to detect and destroy cancer cells carrying one of these defined cancer antigens.
According to Dr. Van den Eynde, this is due in part to the lack of appropriate animal models in which detailed immunological analyses can be performed before and after vaccination. The models we use to investigate cancer vaccines at the preclinical level either have a defined cancer antigen in a transplanted tumor, or they have an original tumor that doesnt have a defined antigen. However, in human clinical studies, we have original tumors with defined antigens. So there has been a need for a mouse model that more closely follows the human model.
Thus the Institute that first cloned mouse and human cancer antigens, allowing the rational design of cancer vaccines, has developed a model in which melanoma with a defined cancer antigen can be induced. The model has been engineered to have several mutations found to occur together in human melanoma, and so closely mimics the genetic profile of cancers treated in the clinic. The team, which is comprised of investigators from Belgium, France and The Netherlands, has already begun characterizing a cancer antigen-specific immune reaction observed before the mice were even vaccinated, which they hope will lead to a further understanding of spontaneous melanoma regressions.
Dr. Jill ODonnell-Tormey, Executive-Director of New Yorks Cancer Research Institute, which was founded in 1953 specifically to foster cancer immunology research, believes that this model may yield information crucial for cancer vaccines for other tumor types and not just melanoma. We have clinical trials for cancer antigens for sarcoma, for melanoma, and for breast, prostate, lung and ovarian cancers. Were learning a lot from these trials, but we could learn a lot more if we have a model like this, which selectively expresses each of our target antigens. Just one example might be the analysis of the immune response to cancer antigens during the early stages of cancer onset and progression, which might indicate if there is an optimum time for vaccination.
Publication:
Cancer Research, the journal of the American Association of Cancer Research
On the web:
www.licr.org
|
Advertise in this space for $10 per month.
Contact us today.
|
|
Subscribe to Melanoma Newsletter
|
|
Additional information about the news article
|
This work was conducted by investigators from the: Brussels Branch of the Ludwig Institute for Cancer Research (LICR), Brussels, Belgium; Cellular Genetics Unit of the Catholic University of Louvain, Brussels, Belgium; Centre of Biomedical Genetics, and Divisions of Molecular Genetics and Experimental Animal Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands; Immunology Center of Marseille-Luminy, National Center for Scientific Research/National Institute of Health and Medical Research, University of the Mediterranean, Marseille, France.
|
Feedback
|
For any corrections of factual information, to contact the editors or to send
any medical news or health news press releases, use
feedback form
|
Top of Page
|