1. Allergy hypothesis: Allergies reveal the infections we have. Severe allergies and infections can be matched up: peanut and Staph, bee and T.gondii, daisy and Clostridium, poison ivy and spirochetes. If an infection can be killed by a compound or inhibited by the compound our immune system sees the interaction and we associate all the compounds present with the infection. If an infection makes a pigment from a compound we will react to that too. For example aflatoxin with peanuts could cause staph to counter respond. Our immune system would identify everything there at the scene of the crime as part of the infection.
2. Quorum hypothesis: Infections talk using quorums and these quorums interfere with our body's pathways. ( for example mycobacteria's cGMP causes such things as type 2 diabetes, high cholesterol, and synuclein bodies)
3.. Autoimmune cross-targeting hypothesis: The Cross-targeting of simultaneous infections on one tissue, one infection inside and one infections outside, triggers autoimmunity. Antibodies or chemicals/drugs can replace one of the infections. By antibodies I mean even those triggered by vaccines. For example a flu virus inside of the pancreas and e.coli latching on to the outside could trigger type one diabetes.
4. Co-carcinogenesis: a virus and a carcinogen together cause cancer. Taking Francis Peyton Rous’ hypothesis further, the carcinogen is a polymerase inhibitor which binds the viral polymerase with higher affinity. Thus the DNA methylation state has been changed but the virus is no longer viable. DNA damage does not cause most cancers, the interaction of carcinogens and viruses do. Further these cancers wear the receptors that the virus that triggered it used to enter and the characteristics of the cancer will be from the receptor's pathways.
5. Barrier crossing infections are ones that can cross the intestine or the blood brain barrier causing gluten sensitivity with the hole they leave behind. This explains the gluten sensitivity of Schizophernia from T.gondii, Celiac disease from e.coli, Tourettes from staph, and crohn’s from mycobacteria.
6. Viral families use receptor families. Influenzas use dopamine receptors. HPVs use Cannabinoid receptors. Herpes viruses use estrogen and estrogen-like receptors. Flaviviruses use melanocortin receptors. Polyomaviruses use serotonin receptors.
7. Aflatoxin like compounds cause tau bodies. ALS and picks disease are caused by different infections but both have tau. Both infections secrete an aflatoxin like compound. Vitamin D is protective against it because aflatoxin uses the vit D receptor.
8. Pituitary tumors are caused by an infection releasing butyrolactones which interfere with normal GABA signals and cause the immune system to confuse nerves with the infection. (or someone taking too many GHB sleeping pills)
9. The receptors used by a virus when triggering autoimmunity cause pathways to be activated which makes the various types of one autoimmune disease. There are 3 types of schizophrenia which match up with the 3 receptors use by the 3 herpes viruses. (sort of a continuation of 6)
The receptor pathway triggered by a virus involved in an autoimmune disease can cause symptoms of the disease that will be distinct. Example: The 3 types of schizophrenia has all 3 herpes virus families and each receptor activated can be matched to symptoms. Estrogen-related receptor and disorganized symptoms for example. 3 receptors used equals 3 types of schizophrenia
10. Alzheimer's disease is caused by damage to the mitochondria: alpha-herpes family, diacetyl, inherited and linked to down syndrome, or radiation damaged mitochondria.
11. Postural orthostatic tachycardia could be caused by reoviruses and the adrenergic receptors they bind.
12. The HLAs are mailboxes for T cells from different areas of the cell. HLA-A is the nuclear mailbox. HLA-B is the mitochondria's mailbox. HLA-C is the endoplasmic reticulum's mailbox. HLA-DR is the cytosol's mailbox for RNA viruses.
HLA-DQ is the cytosol's mailbox for non-encapsulated viruses there. HLA-DP is the plasama membrane mailbox?
The TLR 7 / 9 butterfly nets for DNA in the mitochondria and nucleus trigger TGF-B1 which causes B cells to express MHC1 which are the HLA-A and HLA-B.
HLA-DQ is the cytosol's mailbox for non-encapsulated viruses there. HLA-DP is the plasama membrane mailbox?
The TLR 7 / 9 butterfly nets for DNA in the mitochondria and nucleus trigger TGF-B1 which causes B cells to express MHC1 which are the HLA-A and HLA-B.
13. Carcinogens use certain receptors to get into cells which matches them up with specific cancers.
14. TLRs, toll like receptors, are the innane immune system of nets catching conserved molecules in a non specific way but identifying the region as well as general type of infection. Like HLAs they exist in the different areas of the cell. When the internal viral seeking TLRs are activated the IFN matches the region they are in thus the appropriate HLA is produced helping to find the exact culprit.
15. TLRs send IFNs which tells infected cells to express the corresponding HLAs and macrophages to wear the corresponding TAMs (hands to grab infected cells) TAMS: tyro T , axl A , mer M
Golgi TLR3 IFN lamda HLA-D Tyro3
Nucleus/ Mito TLR7/9 IFNalpha HLA-A HLA-B Mer
Endoplasmic R TLR 8 IFNgamma HLA-C Axl
( Cytosol TLR4 IFNbeta which is not an endosome tlr and carried out by Fibroblasts for bacterial infections that enter host cells )
( Cytosol TLR4 IFNbeta which is not an endosome tlr and carried out by Fibroblasts for bacterial infections that enter host cells )
Because an infected ER means little gets to the surface of a host cell the Natural killer cells step in here and secrete IFNgamma. (note that low levels of IFN gamma is secreted to favor MHC2)
Cytosolic viruses go through the golgi before exiting which is why they trigger TLR3.
Cytosolic viruses go through the golgi before exiting which is why they trigger TLR3.
16. Nuclear viruses awaken embryonic Hervs. They do so by methylating or demethylating DNA. If the virus family demethylates the cancer will be aggressive while the methylating viruses are slow growing. (Cancer occurs when a carcinogen inhibits the viral polymerase..so the virus opens the DNA up but can't use it)
17. Bacterial infections will hide inside of host cells like viruses. Hypothesis: Like the IFN cytokines there should be cytokines that signify where in the host cell they are hiding. Mycoplasmas nest inside the ER, chlamydia hide in vacuoles, salmonella hide in the golgi, and mycobacteria sit in the cytosol. The cytokines seem to match up the features of an infection family with where they hide inside.
For example infections that use modulins tend to move into vacuoles when infecting the host so TLR2 triggers il-23 which then (in hypothesis 20) triggers TGF3 which repairs vacuoles.
18. Could there be 4 different types of asthma caused by different infections which could be diagnosed using cytokine patterns and the allergies present in the host.
19. The problem concerning autism and vaccines could be solved if autism is viewed as an autoimmune disease. The autoimmune cross-targeting hypothesis when applied to autism reveals there could be 3 different types of autism:
Group Flu and RA : frontal lobe autism
Group DTP (tetanus) and HHV6 : temporal lobe autism
Group MMR and sutterella/ campylobacteria: cerebellum autism
Two of these have been linked to vaccines the MMR and the DTP.
Combining the notion that viruses use receptors to enter cells with the notion that "parts" of a virus can set off autoimmunity on the tissue one can only conclude that what is contaminating vaccines setting off autoimmunity are the tiny pieces the virus uses to bind the receptors. Running vaccine solutions through binding columns of the receptors could "clean " the vaccine of the one piece that triggers the autoimmunity.
20. TGF-Beta has been linked to both embryogenesis and cancer as well as the immune system. The area an infection could be damaging causes a specific TGF-B to repair the area. First the TLR butterfly net is triggered by the infection.
TLR9 or TLR7 trigger TGF-B1 which stimulates the mitochondria to grow and smad to the nucleus for DNA repair.
TLR2 triggers TGF-b3 because the infections that use vacuoles tend to be the same ones that use modulins,
TLR-6 which binds lipoproteins found on gram positive bacteria and mycobacterias which divide in the cytosol triggers TGF-b2 which encourages Tcells to check the cytosol of cells,
finally TL3 of the golgi triggers TGf-B4. TGF-B4 stimulates growth of the golgi.
21. T h17 cells are involved in second pops. When does this happen? When large infections move inside of host cells or viral infections are hiding inside of the mitochondria or nucleus. When the viruses are not visible in the cytosol or ER which would be visible when the host cell is popped. Thus a "second popping" must occur.
il-6 and il-23 trigger Th17 to release il-22
note that il-6 is a "reset all in immune respose where phagocytes and TH1 are triggered"and il-23 are released by phagocytes when they can't find the infection they are looking for
il-21 and TGF-b1 trigger the release of il-26 and il19
note that TLR7/9 release TGF-b1 and Tcells release il-21 when activated
22. The type of Lambda IFN matches up with the type of virus going through the golgi. (looks like all viruses go through the golgi before exiting even when they start in different areas)
IFN lambda1 Nuclear virus
IFN lambda2 Mitochondrial virus
IFN lambda 3 cytosolic virus
23. Hypothesis: the TNF family is involved with infections of the immune system itself. Bcells wear TNF-beta(lymphotoxin-alpha) and secrete it at the peyer patches interacting with FDC. This can be seen with viral infections that invade Bcells. Macrophages wear TNF-c (lymphotoxin-beta)when they are infected with bacterias. Macrophages (and other APC) secrete TNF-alpha when infected with either a virus or a bacteria. They key here is that TNF-c receptors on Mast cells switch the focus of the mast cell. They normally secrete cytokines geared at viruses but after lymphotoxin-beta receptor activation they secrete il-6, il-4, and TNF-alpha.
24. The il-20 family of cytokines are H+ pores leaking the H+ our of their assigned membranes
il-20 plasma membrane
il-22 vacuoles
il-24 golgi
il-26 nuclear membrane
il-19 mitochondria
These are used by Th17 to pop membranes. The il-20 cytokines could also used for differentiation for example il-19 converting Th1 to Th2.
17. Bacterial infections will hide inside of host cells like viruses. Hypothesis: Like the IFN cytokines there should be cytokines that signify where in the host cell they are hiding. Mycoplasmas nest inside the ER, chlamydia hide in vacuoles, salmonella hide in the golgi, and mycobacteria sit in the cytosol. The cytokines seem to match up the features of an infection family with where they hide inside.
For example infections that use modulins tend to move into vacuoles when infecting the host so TLR2 triggers il-23 which then (in hypothesis 20) triggers TGF3 which repairs vacuoles.
18. Could there be 4 different types of asthma caused by different infections which could be diagnosed using cytokine patterns and the allergies present in the host.
19. The problem concerning autism and vaccines could be solved if autism is viewed as an autoimmune disease. The autoimmune cross-targeting hypothesis when applied to autism reveals there could be 3 different types of autism:
Group Flu and RA : frontal lobe autism
Group DTP (tetanus) and HHV6 : temporal lobe autism
Group MMR and sutterella/ campylobacteria: cerebellum autism
Two of these have been linked to vaccines the MMR and the DTP.
Combining the notion that viruses use receptors to enter cells with the notion that "parts" of a virus can set off autoimmunity on the tissue one can only conclude that what is contaminating vaccines setting off autoimmunity are the tiny pieces the virus uses to bind the receptors. Running vaccine solutions through binding columns of the receptors could "clean " the vaccine of the one piece that triggers the autoimmunity.
20. TGF-Beta has been linked to both embryogenesis and cancer as well as the immune system. The area an infection could be damaging causes a specific TGF-B to repair the area. First the TLR butterfly net is triggered by the infection.
TLR9 or TLR7 trigger TGF-B1 which stimulates the mitochondria to grow and smad to the nucleus for DNA repair.
TLR2 triggers TGF-b3 because the infections that use vacuoles tend to be the same ones that use modulins,
TLR-6 which binds lipoproteins found on gram positive bacteria and mycobacterias which divide in the cytosol triggers TGF-b2 which encourages Tcells to check the cytosol of cells,
finally TL3 of the golgi triggers TGf-B4. TGF-B4 stimulates growth of the golgi.
21. T h17 cells are involved in second pops. When does this happen? When large infections move inside of host cells or viral infections are hiding inside of the mitochondria or nucleus. When the viruses are not visible in the cytosol or ER which would be visible when the host cell is popped. Thus a "second popping" must occur.
il-6 and il-23 trigger Th17 to release il-22
note that il-6 is a "reset all in immune respose where phagocytes and TH1 are triggered"and il-23 are released by phagocytes when they can't find the infection they are looking for
il-21 and TGF-b1 trigger the release of il-26 and il19
note that TLR7/9 release TGF-b1 and Tcells release il-21 when activated
22. The type of Lambda IFN matches up with the type of virus going through the golgi. (looks like all viruses go through the golgi before exiting even when they start in different areas)
IFN lambda1 Nuclear virus
IFN lambda2 Mitochondrial virus
IFN lambda 3 cytosolic virus
23. Hypothesis: the TNF family is involved with infections of the immune system itself. Bcells wear TNF-beta(lymphotoxin-alpha) and secrete it at the peyer patches interacting with FDC. This can be seen with viral infections that invade Bcells. Macrophages wear TNF-c (lymphotoxin-beta)when they are infected with bacterias. Macrophages (and other APC) secrete TNF-alpha when infected with either a virus or a bacteria. They key here is that TNF-c receptors on Mast cells switch the focus of the mast cell. They normally secrete cytokines geared at viruses but after lymphotoxin-beta receptor activation they secrete il-6, il-4, and TNF-alpha.
24. The il-20 family of cytokines are H+ pores leaking the H+ our of their assigned membranes
il-20 plasma membrane
il-22 vacuoles
il-24 golgi
il-26 nuclear membrane
il-19 mitochondria
These are used by Th17 to pop membranes. The il-20 cytokines could also used for differentiation for example il-19 converting Th1 to Th2.
