autoimmune disease tagged posts

Highlights •Ablation of IRF4 induces transplant acceptance by establishing T cell dysfunction •IRF4 represses PD-1, Helios, and other molecules associated with T cell dysfunction •Irf4‒/‒ T cell dysfunction is initially reversible but later becomes irreversible •Trametinib inhibits IRF4, abrogates EAE development, and prolongs allograft survival

Wenhao Chen, Ph.D., a scientist in the Immunobiology and Transplant Science Center at the Houston Methodist Research Institute, and his colleagues have identified a critical switch that controls T-cell function and dysfunction and have discovered a pathway to target it...

Blood cell analysis identifies 1000s of disease-related genes. Using a pioneering technique developed at the Babraham Institute, results are beginning to make biological sense of the mountains of genetic data linking very small changes in our DNA sequence to our risk of disease. Discovering these missing links will inform the design of new drugs and future treatments for a range of diseases.

Comparing the genome sequences of 100s of 1000s of patients and healthy volunteers has revealed single-letter changes found more frequently in the DNA sequences of individuals with specific diseases. In most cases, the disease-linked changes occur in the large swaths of DNA located between genes, ie junk DNA...

This is a schematic of how a “chimeric autoantibody receptor,” or CAAR, that displays fragments of the autoantigen Dsg3 helps fight an autoimmune disease called pemphigus vulgaris, a condition in which a patient’s own immune cells attack Dsg3, which normally adheres skin cells. Credit: Christoph T. Ellebrecht, MD, Perelman School of Medicine, University of Pennsylvania

Preclinical study shows that engineered T cells can selectively target the antibody-producing cells that cause autoimmune disease. The autoimmune disease the team studied is pemphigus vulgaris (PV), a condition in which a patient’s own immune cells attack a protein called desmoglein-3 (Dsg3) that normally adheres skin cells...

New research shows the presence of saturated fats resulted in monocytes, a white blood cell, migrating into the tissues of vital organs. Received wisdom on the health risks of eating saturated fat has been called into question recently. This new research supports the view that excessive consumption of saturated fat can be bad for us.

Scientists from Imperial College London studied mice that have an unusually high level of saturated fat circulating in their blood. The newly arrived monocytes could worsen tissue damage because they may exacerbate ongoing or underlying inflammation, but this aspect is still under study.
“The mice we studied were treated with a drug that caused them to accumulate extremely high levels of fat in their blood...