Allergies Turned Off

This is extremely important work.  For whatever reason food allergies and autoimmune disease is a significant problem that has to be mastered.  Avoidance is only part of the answer and an unsatisfactory one that still sees many deaths.  Another obvious one that is very important is the allergy to bee stings.  This often arrives in the mid career of someone hugely vulnerable like a farmer.

Importantly this approach is working and they are also attempting to use microparticles in order to avoid using white blood cells which would need to be customized.

The open question remains about how long lasting this procedure actually is.  It would be nice if the whole immune system adopts the improvement.  At least this is progress and for these allergies, progress has been scant.

From the description it appears plausible that the correction should solve all such allergies because it rebalances the system away from the dangerous modes.  Unlikely as it may seem, and certainly not suggested here, it is plausible that a one size fits all solution is possible for allergies.  This is actually suggested by the detailed description of allergic presentations.

Peanut Allergy Turned Off by Tricking Immune System

 OCTOBER 13, 2011

http://nextbigfuture.com/2011/10/peanut-allergy-turned-off-by-tricking.html

Researchers have turned off a life-threatening allergic response to peanuts by tricking the immune system into thinking the nut proteins aren’t a threat to the body, according to a new preclinical study from Northwestern Medicine. The peanut tolerance was achieved by attaching peanut proteins onto blood cells and reintroducing them to the body -- an approach that ultimately may be able to target more than one food allergy at a time.

It’s the first time this method for creating tolerance in the immune system has been used in allergic diseases. It has previously been used in autoimmune diseases.

The approach also has a second benefit. It creates a more normal, balanced immune system by increasing the number of regulatory T cells, immune cells important for recognizing the peanut proteins as normal.

“T cells come in different ‘flavors’,” Bryce said. “This method turns off the dangerous Th2 T cell that causes the allergy and expands the good, calming regulatory T cells. We are supposed to be able to eat peanuts. We’ve restored this tolerance to the immune system.”

Peanut allergies often cause life-threatening allergic reactions, called anaphylaxis. Each year there are between 15,000 and 30,000 episodes of food-induced anaphylaxis and 100 to 200 related deaths in the United States, according to the National Institutes of Health. There is no safe treatment to protect people from a severe allergic reaction to food.

When an allergic person eats a peanut, the proteins are absorbed through the intestine and can activate a life-threatening, full-body immune response. This includes constriction of the airways, low blood pressure and/or shock and can lead to loss of consciousness and death.

Using a mouse model that mimics a life-threatening peanut allergy (which the Northwestern team developed several years ago), researchers attached peanut proteins onto white blood cells called leukocytes and infused those back into the mice. After two treatments, the mice were fed a peanut extract. They did not have the life-threatening allergic reaction because their immune system now recognized the protein as safe.

“Their immune system saw the peanut protein as perfectly normal because it was already presented on the white blood cells,” Bryce said. “Without the treatment, these animals would have gone into anaphylactic shock.” Bryce thinks more than one protein can be attached to the surface of the cell and, thus, target multiple food allergies at one time.

In the second part of the study, Northwestern researchers used the same approach with an egg protein, which was to provoke an immune response –- similar to an asthma attack -- in the lungs. They attached the proteins to white blood cells and infused the cells back into the mice. When the mice inhaled the asthma-provoking egg protein, their lungs didn’t become inflamed. 

“This is an exciting new way in which we can regulate specific allergic diseases and may eventually be used in a clinical setting for patients,” said Miller, the Judy Gugenheim Research Professor at the Feinberg School.

Miller also has used the same approach in autoimmune diseases. His previous published research has shown the same technique to stop the progression of multiple sclerosis and type 1 diabetes, both autoimmune diseases, in animal models. This approach is currently being tested in multiple sclerosis patients in a phase I/IIa clinical trial.

For autoimmune diseases and allergic airway diseases, Miller also is working with microparticles rather than white cells to induce tolerance, because the microparticles are more easily standardizd for manufacturing.