Enhancing the immune system in cancer patients … finally a worthy focus.

Dr. Weeks Comment:  Most experienced clinicians understand that a healthy immune system beats a healthy cancer any day of the week (and twice on Sunday if you faith and attitude are radiant). Yet immune enhancement therapies have long taken a back seat to the cut, burn, poison approach which has given oncology such a poor PR reputation.  Now more interest in immune enhancement is being studied and, of course, corrective approaches (using naturally occurring biochemistry or ortho-molecules) are far safer and more effective than synthetic vaccine adjuvants (like squalene which causes hyper immune responses and auto-immunity!) 

So follow common sense with cancer and use the old tried and true agents to enhance immunity:  exercise (“give me the power to create a fever and I will cure all illness”), oxygen (in all sorts of delivery systems)  improve diet (examples: raw is great, no refined sugar helps) and many other immune enhancement options (www.lowdosenaltrexone.org)  etc  before you start trying to kill cancers. Once you do, remember insulin potentiated cancer therapies:  IPT  see www.iptforcancer.org 


Using The Immune System To Reduce Prostate Cancer Risk

ScienceDaily (Sep. 24, 2009) ”” Immune therapies have been explored as a way to treat cancer after it develops. But a new study from the University of Michigan Comprehensive Cancer Center suggests that genetic risk of prostate cancer can be reduced by rescuing critical immune system cells.

The study was done in mice and would need further validation and extensive testing in the lab before being available for humans. But the results are promising for people with a strong family history of cancer or known cancer genes.Typically, vaccines are based on specific antigens and trigger immunity for a specific pathogen. This is more challenging for cancer as the best lymphocytes that generate immunity to cancer are eliminated during development. In this new study, researchers sought to rescue these key lymphocytes – called high affinity cancer-reactive T cells – during their development.

The study appears online in the Proceedings of the National Academy of Sciences.

The researchers first showed that T cells involved in prostate cancer are deleted because of a gene called lymphotoxin alpha. When the mice lacked lymphotoxin, these T cells came back. These mice become more resistant to prostate cancer. This result suggests that lymphotoxin can be a good target for immune prevention.

Next, the researchers injected a protein targeting lymphotoxin into cancer-susceptible mice. Without treatment, all of these mice will develop prostate cancer, and typically by age 6 months half of them will have metastatic cancer that has spread to distant organs. Although the treated mice still developed tumors, none developed metastases after 30 weeks.

“It appears that the rescued T cells delay tumor formation. It may not be that this approach can prevent cancer altogether, but it can delay the process and slow the aggressive growth and spread of cancer,” says study author Pan Zheng, M.D., Ph.D., associate professor of surgery and pathology at the U-M Medical School.

While this study looked specifically at mice with prostate cancer, the approach has potential for other types of cancer.

“There is a certain population with a high likelihood of getting cancer, and we need better strategies to minimize their risk. This approach may be translated into clinical care for those patients,” Zheng says.

Prostate cancer statistics: 192,280 Americans will be diagnosed with prostate cancer this year and 27,360 will die from the disease, according to the American Cancer Society.

Additional authors include Penghui Zhou, Beth A. McNally, Lizhong Wang, Yang Liu, from U-M; Xiafeng Fang from the Chinese Academy of Science; and Ping Yu, Mingzhao Zhu, and Yang-Xin Fu, from the University of Chicago School of Medicine.

Funding was provided by the National Institutes of Health, Department of Defense Prostate Cancer Research Program.

Reference: Proceedings of the National Academy of Sciences, doi: 10.1073/pnas.0905707106

Adapted from materials provided by University of Michigan Health System.

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