The problem with this is that there’s currently no way to target immune-suppressing drugs to say: “Hey, just stop attacking your own cells, but continue doing everything else an immune system is supposed to do
Allergen immunotherapy, also known as desensitization or hypo-sensitization, is a medical treatment for environmental allergies (such as insect bites) and asthma.[1][2] Immunotherapy involves exposing people to larger and larger amounts of allergens in an attempt to change the immune system’s response.[1]
We do have some limited ability to “train” at least some aspects of the immune system not to attack certain things. I’ve no idea whether that approach can be used for something like this.
No - this is something completely different, unfortunately. Allergen response is mediated by T-helper type 2 (TH2) cells, while autoimmune disorders like diabetes occur through a T-helper type 1 (TH1) pathway.
With allergens, the foreign body will bind to antigen receptors on professional antigen presenting cells (usually dendritic cells), which will then present the bound antigen to TH2 cells. These will then release a particular type of chemical called cytokines that will signal the B cells to produce a shit load of IgE antibodies tailored for the particular molecular pattern identified. The IgE will bind to the antigen and also to basophils and mast cells, which will secrete a bunch of chemicals, including histamines. This is what causes you to get all itchy. It’s also what causes swelling (such as when someone with a peanut allergy feels their throat closing up when they find out their snack had peanuts in it).
With Type 1 Diabetes, TH1 cells will recognize patterns on the surface of your islet cells, and will then release a different set of cytokines that will attract cytotoxic T cells (TC) to the area. These will bind to the surface of the islet cells, and will release a cocktail of chemicals that will kill the cell.
The mechanism by which allergen immunotherapy works is that it slowly trains your immune system to shift from a TH2-dominated response to a TH1-dominated response for that particular molecular pattern. This means that your body will treat the foreign substance as more of an invading pathogen (like a bacteria, for example) than an allergen, so there will not be the huge release of IgE antibodies, and consequently, far fewer mast cells and basophils releasing histamines. The precise mechanism of how this works is too complicated for this discussion, but suffice it to say we’re dealing with a completely different biological pathway than with self / non-self recognition, like what’s going on with autoimmune disorders.
https://en.wikipedia.org/wiki/Allergen_immunotherapy
We do have some limited ability to “train” at least some aspects of the immune system not to attack certain things. I’ve no idea whether that approach can be used for something like this.
No - this is something completely different, unfortunately. Allergen response is mediated by T-helper type 2 (TH2) cells, while autoimmune disorders like diabetes occur through a T-helper type 1 (TH1) pathway.
With allergens, the foreign body will bind to antigen receptors on professional antigen presenting cells (usually dendritic cells), which will then present the bound antigen to TH2 cells. These will then release a particular type of chemical called cytokines that will signal the B cells to produce a shit load of IgE antibodies tailored for the particular molecular pattern identified. The IgE will bind to the antigen and also to basophils and mast cells, which will secrete a bunch of chemicals, including histamines. This is what causes you to get all itchy. It’s also what causes swelling (such as when someone with a peanut allergy feels their throat closing up when they find out their snack had peanuts in it).
With Type 1 Diabetes, TH1 cells will recognize patterns on the surface of your islet cells, and will then release a different set of cytokines that will attract cytotoxic T cells (TC) to the area. These will bind to the surface of the islet cells, and will release a cocktail of chemicals that will kill the cell.
The mechanism by which allergen immunotherapy works is that it slowly trains your immune system to shift from a TH2-dominated response to a TH1-dominated response for that particular molecular pattern. This means that your body will treat the foreign substance as more of an invading pathogen (like a bacteria, for example) than an allergen, so there will not be the huge release of IgE antibodies, and consequently, far fewer mast cells and basophils releasing histamines. The precise mechanism of how this works is too complicated for this discussion, but suffice it to say we’re dealing with a completely different biological pathway than with self / non-self recognition, like what’s going on with autoimmune disorders.