Patients with lupus have an imbalance in a crucial chemical pathway in their bodies, according to a Nature study published recently.
Researchers found that this imbalance produces more disease-causing cells that promote lupus. If this chemical imbalance can be corrected, they believe lupus can be reversed.
Current lupus treatments often target symptoms or broadly suppress the immune system, leading to side effects. The researchers believe targeting the specific chemical imbalance identified could more effectively treat lupus without systemic immunosuppression interventions.
Lupus is a chronic autoimmune disease that causes the body to attack its own tissues and organs, including the joints, skin, kidneys, blood cells, brain, heart, and lungs.
There is currently no cure for lupus.
The chemical that researchers identified is the aryl hydrocarbon receptor (AHR).
AHR is a key protein involved in the imbalance of immune cells in lupus patients. It regulates the body’s response to environmental pollutants, bacteria, and metabolites. While AHR is present in all cells, it is not always active.
Researchers found that lupus patients have reduced AHR activity. This reduction leads to an increase in follicular and peripheral T helper cells, which are involved in inflammation and autoimmunity.
However, when AHR activity increases, these T-cells are reprogrammed to be T-cells that promote wound healing and barrier protection.
Dr. Jaehyuk Choi, associate professor of dermatology at Northwestern University Feinberg School of Medicine, and the study’s senior author, explained to sources that AHR can be compared to “a molecular switch” that determines the fate of immune cells.
By developing therapeutics that target AHR in rogue T-cells, researchers believe they may be able to reverse lupus.
Dr. Choi and Dr. Deepak Rao, an assistant professor of medicine at Harvard Medical School, expressed their surprise at discovering that AHR could be vital in reversing autoimmunity, given that the receptor had no known connection to it.
Dr. Rao, who is also a senior author of the study, added that it was initially surprising to find that a T-cell involved in wound healing would be the opposite of an autoimmune T-cell.
“Those two T-cell populations with those two functions are not obviously connected or related,” he said. He added that he could not have predicted that when wound-healing T-cells increased, autoimmune T-cells would decrease, and vice versa.
Follicular and peripheral T helper cells have long been known to play a major role in driving lupus, Dr. Rao told The Epoch Times.
In lupus, the patient’s body produces autoantibodies, antibodies that attack self-tissues. B-cells generate these autoantibodies under the control of rogue autoimmune T-cells.
Therefore, by converting these autoimmune T-cells into cells involved in wound healing, the production of autoantibodies is reduced, thereby decreasing autoimmunity.
“It is almost like a cell streamline, where if you can block one part, then the downstream is blocked,” Dr. Choi explained.
He highlighted the study’s findings demonstrating that adding AHR to rogue T-cells in cell culture transforms them into wound-healing cells. These reprogrammed cells can no longer help B-cells make autoantibodies.
Dr. Rao added that these rogue T-cells are also present in other autoimmune conditions, like rheumatoid arthritis, raising the question of whether drug targets for these cells may apply to such conditions.
