Rheumatoid Arthritis Leads To New Chronic Inflammation

According to the recent reports from a new group, experts reveal that our researchers are still in the process of linking the T cell dysfunction with a metabolic deficiency seen in rheumatoid arthritis.

Rheumatoid Arthritis Leads To New Chronic Inflammation

Rheumatoid arthritis is a systemic autoimmune disease, particularly with the symptoms of joint damage and alteration of systematic organs. It’s a potential destructive disease with an impact on patient quality of life. The Newer therapies for patients have not resulted in better results.

Rheumatoid Arthritis Leads To New Chronic Inflammation

Rheumatoid Arthritis is an age-old medical condition that trouble millions of people globally. One suffers from this ailment has to counter some more medical conditions also as per new research carried out by experts.

RA leads to chronic inflammation if not treated rightly in the primary stage, and hence one has to undergo severe pain in routine activities such as standing, walking and carrying out exercises also mentioned one of the team members from the research team. 

In Rheumatoid arthritis, particularly hand and feet or synovial joint are involved with more joint damage, which can disrupt a person quality and function of life. It’s a chronic inflammatory disorder of joints. Sometimes a person is shown with a wide variety of damaged body systems involving skin, eyes, lungs, heart, and many. 

In patients with chronic rheumatoid arthritis disorder, helper T cells have low levels of specific amino acids, which leads to cellular miscommunication. But supplying with more active amino acids may provide a new therapeutic strategy to enhance the autoimmune system.

Rheumatoid arthritis is highly characterized by chronic inflammation blockers involving a high level of cytokine, which acts as a tumor necrosis factor. The necrosis factor leads to the death of the cell. 

According to a popular and famous immunologist and a rheumatologist, Cornelia Weyand states that tumor necrosis factor has been used as a therapeutic target to treat autoimmune disease and tissue inflammation for the last 25 years of study.

The introduction of tumor necrosis factor changes the management process of inflammatory disease. Their introduction blocked the action of TNF in the inflamed tissue, but cytokine production could not be stopped. Thus the treatment of the root cause of TNF-induced disease remains untreated.

After the beginning of investigation with helper T cells by famous Dr. Weyand’s team collected data sets about how your immune system coordinates and responses to invader encounters. From their study, they state that the helper T cells coordinating with the immunity system remain in the body after infection to help and respond quickly. 

These helper T cells not just remember the previous encounter with a pathogen but also memorize what mistakes they have made in response to the pathogen so that occurrence of the same mistake would be prevented. 

T cells are the part of the immune system that focuses on protection from foreign particles. After encountering a specific antigen, they attack the antigen. T cells play a crucial role in the protection of foreign substances. Its main function is to respond to a harmful allergen for the body and maintain immune homeostasis.

Surgical teams associated with rheumatologists researchers found the helper T cells are the primary source of tumor necrosis factors. Several clinical trials are performed on mouse cells as a model to determine the defect of the T cells in their mitochondria.

Through a series of research and experiments, we have discovered that the absence of amino acid aspartate rheumatoid arthritis T cells behaves differently. Aspartate acts as a messenger between the mitochondria and the endoplasmic reticulum. That’s why the risk of tumour necrosis rises in the absence of aspartate.

Therefore in patients repairing mitochondrial defects is necessary to suppress the tissue inflammation successfully.

United States trained Investigative Journalist, Clinical Pharmacist, PR Specialist, and Activist.


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