|HLA DR Haplotye Testing|
This page contains educational material about HLA DR Haplotype testing.. This information is for educational purposes only. Nothing in this text is intended to serve as medical advice. All medical decisions should be made only with the guidance of your own personal medical authority. I am doing my best to get this data up quickly and correctly. If you find errors in this data, please let me know.
Genetic HLA DR haplotypes
People with CIRS due to water-damaged buildings have HLA issues that make them susceptible. Without HLA issues, they can remove mycotoxins from their bodies.
HLA stands for Human Leukocyte Antigen (foregin body). It is the name given to the Major Histocompatibility Complex (MHC) in humans. The HLA complex is a series of genes on human chromosome 6 that codes for proteins that are unique to each individual. They are centrally involved in the actions of the immune system. HLA-DR's primary function is to present potentially foreign particles (antigens) to the immune system so the immune system can incapacitate and remove it from the body. HLA-DR is found on the cell surface of certain white blood cells that we call antigen presenting cells.
The primary function of HLA-DR (Human Leukocyte Antigen - antigen D related) is to present peptide antigens (forein bodies usually), to the immune system. The white blood cells with HLA-DR binds the antigen to a DR molecule on the outside of the white blood cells body. These white blood cells are called antigen presenting cells (APCs). Antigen presenting cells with such names as macrophages, B-cells and dendritic cells present antigens to other parts of the immune system. Basically, the APCs grab the antigen, process it and take small parts of it and present it to other white blood cells via the DR molecule on its cell surface. It is as if to say, "Hey guys, I just found this possible invader, you need to do something about it." (Some people think of these cells as pacmen type cells that tell the immune system when there is somethig bad in the body.) When white blood cells called T cells see this antigen presented to them, they are able to react by protecting the body against this antigen if that is the appropriate reaction. This ramps up the immune system to remove the antigen with various methods. However, sometimes this does not work properly. Sometimes when a person has a particluar type of HLA-DR haplotype their APCs are not able to present the antigens properly. This means that the immune system does not end up removing the antigen. The immune system starts to react but does not follow through. This causes an inflammatory state in the body.
People with mold susceptabilties have variants of HLA DR Haplotypes that render them unable to react properly. (The primary mold-susceptible types are 7-2/3-53, 13-6-52 A/B/C, 17-2-52A, 18-4-52A.) This makes their immune system unable to present the antigens appropriately. It is thought that 25% of the population is under-reactive. There are additionally other types of HLA-DR haplotypes that are found to inadequately react to other biotoxins besides mold. They include biotoxins from jellyfish stings and bee venom. When a person has specific HLA-DR haplotypes that do not react appropriate to mold toxins and they are exposed to mold toxins, their immune system will not react appropriately as mentioned previously. It sets into motion an inadequate reaction that does not remove the toxins, but it does initiatate an inflammatory state in the body that can cause a lot of symptoms. However, the mold toxins are never removed. They stay in the body and cause the immune system to continuously be on alarm as the APCs ineffectively try to get the rest of the immune system to remove the mold toxins. The person ends up being in a continuous inflammatory state.
HLA-DR testing is used to identify people who are unable to remove certain biotoxins and are more susceptible to those types of biotoxin illness. HLA
Dr Ritchie Shoemaker has completed extensive research on mold susceptible people to identify the HLA haplotypes that cause this susceptibility to mold toxins. The people with these specific haplotyes are not able to remove the mycotoxins from their body like other folks. These people can end up with a condition called Chronic Iflammatory Response Syndrome (CIRS) due to water-damaged buildings.
The research done by Dr. Shoemaker showed his paitents with CIRS due to water-damaged buildings shared specific HLA-DR haplotypes. If a person has chronic fatigue type symptoms and a mold susceptibility is suspected, this test can show if they are indeed one of the susceptable haplotyes. Usually, they are first given a VCS test. If they do not pass this test and they have a history of being exposed to a water-damaged building, an HLA-DR haplotype test will give an idication to the practitioner that this patient may be reacting to mold mycotoxins. Other tests are also usually used as indicators.
There are a variety of HLA DR haplotypes that make people more susceptible to certain illnesses that have been identified by Dr. Shoemaker and other practitioners as being related to certain illnesses. I am going to list those that I know of here.
Susceptible to mold: 7-2/3-53, 13-6-52 A/B/C, 17-2-52A, 18-4-52A
Low risk of mold susceptibility: 7-9-53, 9-9-53, 12-7-52B
Sucsecptible to multiple illnesses: 11-3-52B, 12-3-52B, 4-3-53, 14-5-52B
Susceptible to Chronic Lyme Borreliosis: 15-6-51,16-5-51
Susceptible to Dinoflagellates (toxic algae): 4-7-53, 4-8-53
Sesceptible to Chronic Fatigue Syndrome: 4-3-53, 11-3-52B
Susceptible to MS: 15-6-51
Susceptible to MARCoNS: 11-7-52B
Susceptible to Gardisil vaccine reactions: 11-3-52B
Susceptible to chronic fatigue from Lymerix vaccine for Borrelia: 4-3-53 (subtypes 0401,0402 and 0404 for DRB1 are the worst.)
More likely to have low MSH: 1-5
Susceptible to Celiac: 17-2-52A,B,C, 7-2-53
More likely to have hypermobility and autoimmunity: 11-3-52B
Causes trouble with Urine Testing for Mycotoxins: Please realize that people with these HLA haplotypes have trouble identifying mycotoxins as antigens in their bodies. This means that they will have trouble removing them through the bile and intestinal system or the urine. This means a urine test for mycotoxins may come up negative in a person who has those mycotoxins in their body if they have haplotypes that are not good at tagging the mycotoxins as antigens. Sometimes the mycotoxins can be mobilized by use of a sauna or a challange test of glutathione.
HLA-DR Haplotypes by PCR is the test necessary to identify haplotypes and LabCorp is the lab I use.
Here is a description that helps to understand HLA-DR activity although it is not really what is going on.
Imagine the HLA-DR molecule on the outside of the white blood cell cell wall as a little hand they are holding out. Also imagne that the cell picks up particles around it, ingests it and then regurgitates out parts of it onto the hand. The cell then presents this to other immune cells who examine it and decide what they should do about the foreign particles presented to them. Their decision depends on both what the HLA-DR molecule is handing to them as well as other indicators in their environment. Once they decide, they can morph into an advanced type of WBC that will allow it to handle the situation. This is not exactly what happens but close enough to explain it. For a scientific explanation you can read above or even get more details at the University of South Carolina.
I found someone has set up an HLA-DR calculator to help people deciphor there tests themselves. I have no idea if it is completely accurate, but I am listing a link here.
Could Glutathione deficiency cause more trouble with this antigen presenting cell?
I would like to mention that there are other factors involved here which could effect this process. For instance glutathione depletion in antigen presenting cells inhibits Th1-associated cytokine production and/or favors Th-2-associated responses. Multiple chemical sensitivities in individuals are associated with decreased Th-1, increased Th-2 response. Mycotoxins (as well as other toxins) can deplete the body of glutathione and could add to the problems with an improper antigen presenting cells activity. So, although HLA-DR haplotypes are seen in these people who have CIRS due to water-damaged buildings, this is only part of the puzzle. They may be starting with an immune system that is not reacting appropriately but in addition this can be made with through environmental factors such as mycotoxins leading to glutathione depletion. See more about mycotoxins and glutathione depletion at the bottom of the glutathione page.
Here is the medical science on how HLA polymorphisms can instigate CIRS due to waterl-damaged buildings:
The MHC (Major Histocompatibility Complex) contains more than 200 genes which are situated on the short arm of chromosome 6 at 6p21.3 The role of HLA molecules is to present peptides to T cells (both CD4 and CD8 T cells), enabling them to recognize and eliminate “foreign” particles and also to prevent the recognition of “self” as foreign.
HLA plays a central role in immune surveillance, and HLA polymorphisms may impact the ability of the immune system to identify foreign or malignant cells and target them for T cell-mediated elimination. HLA class I proteins (HLA-A, -C, and -B) present peptides from endogenous proteins to cytotoxic T lymphocytes. HLA class II proteins (HLA-DRB3/4/5, -DRB1, and -DQB1) present peptides derived from exogenous proteins to CD4+ helper T cells. Downregulation of HLA is a well-defined mechanism of immune surveillance by viral infections and in neoplastic cells. HLA gene polymorphism has been found to be associated with cancer, autoimmune, and infectious diseases.
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