CANCER

Cancer Prevention-Cure with natural low cost high efficiency IUI Individual Universal Immunotherapy C-Life-IUI-CBM-SAV-SAS-SAT.

Natural proven in-vivo process +95% effective can be replicated ex-vivo, with space-time-variables under direct control for +99,99% effectiveness. Cell Bank Medculture can produce quantity/quality Immune cells/antibodies to be exposed to extracted cancer cells, tissue and/or proteins.

Super-Cancer, Super-Virus, Super-Bacteria and Super-Aging are not only not cured by allopathic medicine substance/drug abuse, it is caused/promoted by it. In-vivo Human Biology cures most of it, Ex-vivo Biologic Medicine can cure the rest.

C-Life Cubic Cell Culture Life

Biologic Medicine hardware-software fixed-mobile system to coordinate Individualized Universal Immunotherapy from extracted centrifuged blood/lymph/bone marrow cells/proteins and Cell Bank Medculture ex-vivo permanent multi-function expansion.

IUI Individual Universal Immunotherapy

In-vivo Human immune defense system is proven to be highly efficient +95% and dysfunction symptom inefficiencies are circumstantial to space, time, cancer/pathogen/antibodies/immune cell quantity and variety. These negative circumstances can be corrected ex-vivo with IUI.

Ex-vivo signaling using in-vivo signals can be used to induce cancer cell destruction, antigen extraction, antigen loading to produce antibodies and antigen loaded B/D/T cells. Many strategies can be created and tested ex-vivo, using the same system to distinguish between healthy/unhealthy cells.

Signaling include Cytokines (chemokines), Caspases (Caspase-1/ IL-1ß and IL-183), Damps (Damage Associated Molecular Patterns as ATP, HMGB1, Heat shock proteins), Ligands (cell stress expression Ligands as NKG2D), PHOSPHATIS (PS/PE phosphatidylserine/phosphatietalonamine).

Any strategy that is capable of inducing response from immune cells, antibodies, antigen identification, antigen cell loading ex-vivo can complement the in-vivo proven model to specifically target and replace unhealthy cells while protecting healthy cells, allowing cell/issue/organ/body regeneration.

Checkpoint proteins as CTLA-4, PD-1 and PD-L1 protect healthy cells turning off reception from T-cells, but Cancer/dysfunctional cells may also maintain that function and instead of signaling T-cells for destruction, they maintain healthy cell signaling including these checkpoint proteins.

Artificial distortion copycat monoclonal antibodies by allopathic medicine industry try to distort systemic natural approach of Biologic Medicine, calling antibodies "drugs" with "Xmab-X" names, with patents, abusive high prices/profits to block these checkpoint proteins of cancer and healthy cells.

Most of allopathic treatments, including non-individualized artificial monoclonal cells targeting human proteins, may affect healthy and cancer cells to higher or lesser degree depending on how targeted are their delivery into the body cancer cell tissue/organ.

Individual Human Polyclonal Antibodies produced from plasma B-cells, blood/cell bank to target non-human protein/antigens at many points, are more efficient than current artificial general monoclonal antibodies targeting human proteins at cancer/healthy cell specific point, as CTLA-4, PD-1 and PD-L1.

Natural Individual ex-vivo antigens, antibodies and antigen loaded immune cells can target specific cancer cells in-vivo without affecting healthy cells, which is not the case of allopathic medicine strategies as chemotherapy, radiotherapy, macro surgery and non-individual monoclonal antibodies.

Trying to block/unblock checkpoint proteins of cancer/healthy cells, as all strategies affecting healthy cells and the regeneration process, put Life at risk if the cancer is at advanced stage and risk creating cancer from the treatment in the long run as a side effect. Antigen shouldn't be present in healthy cells.

CBM Cell Bank Medculture

Immune Cells, Antibodies and Antigens can be produced by permanent multi-function individual Cell Bank Medculture, that includes supplementing in-vivo defense system against cancer with ex-vivo space-time-quantity-type variable control leading to +99.99% efficiency.

In-vivo defense system distinguishes unhealthy from healthy cells, so ex-vivo must pursue a similar strategy. Attacking/damaging healthy cells can be equality damaging to cancer patient. Immune regeneration requires Revoking, Repairing, Replacing, Reforming and/or Replicating cells.

SAV Super Auto Vaccine

General Antigen and Individual Antibody produced by Individual IUI/CBM cell bank, identifying antigen of cancer, via multi-strategies proven ex-vivo, loaded into nano intra-skin delivery auto-applied system, as skin patch, sublingual pill and/or nasal spray.

SAS Super Auto Supplement,

Ex-vivo produced nano Human mRNA to produce Human Proteins to produce supplements to help Revoking, Repairing, Replacing, Reforming, Replicating cells. Intra-venal antigen loaded immune cells (B/T/D) can supplement cure/prevention/regeneration, as macro-proteins.

SAT Super Auto Test

Mescope, microfluid saliva, blood, urine, mucus, sweat, tear, can identify cancer proteins/antigens via photonic imaging of cell phone, accessory lenses and network HAI, Human Artificial Intelligent enlargement/analysis, complemented by mini testing in mini-laboratory.