Unraveling MS: How EBV and Genetics Collide
A recent study suggests a mechanism explaining why only a fraction of individuals infected with the Epstein-Barr virus (EBV), which is carried by nearly all humans, develop multiple sclerosis (MS).
MS is an autoimmune disease where the immune system attacks myelin sheaths surrounding nerve fibers. Symptoms can include vision problems, sensory issues, and impaired muscle control. Immunosuppression is a common treatment, but prevention is a primary research goal.
MS is an autoimmune disease where the immune system attacks myelin sheaths surrounding nerve fibers. Immunosuppression is a common treatment, but prevention is a primary research goal.
The Critical Role of EBV and HLA-DR15
Research involving scientists from China, Germany, Switzerland, and the UK identified a critical link between EBV infection and the genetic molecule HLA-DR15. HLA molecules are part of the immune system, helping distinguish between internal and external structures.
When B cells (white blood cells that produce antibodies) are infected with EBV, they present viral components to other immune cells. A key finding is that these viral structures bear a strong resemblance to a protein found in myelin, leading the immune system to mistakenly target and attack myelin protein.
Further investigation revealed that if infected B cells possess the HLA-DR15 molecule, the EBV can modulate these cells to present the myelin protein directly. This indicates that in some MS patients, the immune system is programmed to attack itself due to this viral and genetic interaction.
If infected B cells possess the HLA-DR15 molecule, the EBV can modulate these cells to present the myelin protein directly.
Beyond Genetics: Other Contributing Factors
While HLA-DR15 is considered the most significant genetic risk factor, it is present in only about half of MS patients and does not guarantee disease development.
Other factors like the timing of EBV infection (late childhood or early adulthood), unhealthy diet, vitamin D deficiency, smoking, pollution, shift work, and obesity may also contribute to MS development.
Future Directions: Prevention and Targeted Therapies
Preventative measures, such as a vaccine against EBV, are under investigation. Specialists believe that preventing an initial EBV infection may be challenging, but a vaccine targeting the outbreak of Pfeiffer's disease (mononucleosis) in early childhood, which increases MS risk if symptomatic, could be more feasible. Initial vaccination candidates are currently undergoing trials.
A vaccine targeting the outbreak of Pfeiffer's disease (mononucleosis) in early childhood, which increases MS risk if symptomatic, could be more feasible.
Researchers are also exploring treatments that specifically eliminate immune cells presenting or reacting to EBV components, particularly for MS patients with the HLA-DR15 genetic profile. This represents a significant area of interest for future MS management.