Dendritic Cell Treatment
Working Dendritic Cell Therapy
When first starting this cancer adventure, we noticed that some people responded to Dendritic cell treatment (DC). Being statisticians, we examined the variables of working treatments, found similarities and were able to find a working model. That was eight years ago. Now the treatment variables are commercially available and DC Therapy Clinics should be able to offer a working treatment. Lets look at the AltCancer methodology. Had a hard drive crash so please be patient for the references.
Fact: The immune system will only fight cancer for a specific time period – about 2 years and 2 months. This is for all solid tumor cancers. The theory being cancer resembles normal cells and the body will not fight itself. So, cancer cells in dense tissue areas where macrophages cannot reach may escape detection and after two year proliferate. Also, constant exposure to viruses or environmental triggers lasting longer than two years may also propagate. The immune system stops fighting the infection. (Need Ref)
So the question becomes, how to retrain the immune system to recognize the the cancer? First we must look at how the immune system works. Which leads us to the SPF Micro Organ.
SPF Micro Organ is a newly discovered human organ that surrounds each of our lymph nodes. Its sole job is to examine incoming antigens presented by DC or as some call Antigen Presenting Cells. Basically, DCs find suspicious antigens and bring them in for evaluation. The SPF Micro Organ examines the antigens and pases the information to immune memory cells located deep within the the bone marrow. The immune memory cells say yes or no and pass the information back to the SPF Micro Organ.
If yes, the DC cell passes on the antigen to immature T-Cells located in the lymph node. The immature T-Cells become activated and hunt down the infection. If the answer is no, the SPF Micro Organ does not allow the DC cells to pass on the antigens. This is what happens after two years.
So how to bypass the SPF Micro Organ and immune memory cells. We have noticed three working models.
1. Injecting the DC cells directly into the lymph node. This puts the antigens directly in contact with the T-Cells. They activate and the immune response starts anew. We would like to thank the good people at the Queen Sirikit Breast Cancer Center in Bangkok for pointing this out. Here are two articles showing positive results. This does not mean the treatment is commercially available or that you can receive this treatment. So please do not contact or hound the center. We will examine the variables later.
https://www.bangkokpost.com/life/social-and-lifestyle/2091919/medical-miracle
https://english.redcross.or.th/news/medical-and-health-care-services/5830/
2. One can activate the DCs outside the body before injection. Two signals that attach to the DCs are needed. TNF-alpha and CD40. When these two activators are added to the DC outside the body, it signals the SPF Micro Organ to accept the antigens. Perhaps it adds urgency to the infection. We can thank our friends in China and Stanford for providing insight into the process. At least the correct variables for a working model. Again, we will go over the variables later in the article. The China paper with images is long gone.
Allogeneic IgG combined with dendritic cell stimuli induce antitumour T-cell immunity
https://pubmed.ncbi.nlm.nih.gov/25924063/
3. One can destroy the immune memory cells and then inject the DCs. This is easliy accomplished with high dose chemotherapy. Getting the timing right seems difficult yet there are working examples form Stanford. (Need Ref). Its on Stanford’s cancer website.
So how does one proceed? Our good friends at the Jamie Leandro Foundation are really close. I will assume they are using a DC vaccine in this write up. We contacted them but the staff was unsure. https://jaimeleandrofoundation.org. Their procedure is available for Stage 4 patients who have exhausted all options. AltCancer has shamelessly attached their image explaining the procedure. If the Foundation wants us to remove the image, let us know. But they have an excellent understanding of the process and are more eloquent.
Dendritic Cell Treatment
1. Collect tumor cells with a liquid biopsy. No need to dissect the patient. Tumor cells and Tumor Stem Cells.
2. Conduct intensive DNA sequencing to identify patient specific target antigens.
3. Use AI algorithms to determine the best targets. Insure the targets are on each cancer cell. Also it is more important to analyse Cancer Stem Cells.
4. Have a University review the target findings.
5. Print and expand (multiply) the antigens.
5. Manufacture the DC Vaccine with the manufactured antigens. Be sure to add the correct HLA.
6. Administer the vaccine. Here is where we believe the mistake is being made. Injecting the vaccine into the lymph node will bypass the SPF Micro Organ. Otherwise, the DC is just presenting antigens that the immune memory cells will reject.
7. You should be cancer free in eight months. If no response after four months, try a new set of antigens.
That is about it. Getting done virtually impossible. That is why we have opened sourced the information in the hopes that some ambitious grad student can get funding and preemptively win the Nobel like Barack Obama. Maybe posting a link to his site will get someones attention.
Enjoy the attachment. And thanks again to the Jamie Leandro Foundation for making the explanation easy.
