B cell activating factor could hold key to immune tolerance for hemophilia, study finds
IU School of Medicine Apr 15, 2021
A group of scientists have just made a key discovery that could prevent and eradicate immune responses that lead to treatment failure in about one-third of people with severe hemophilia A.
Hemophilia is the most common severe inherited bleeding disorder in men. The disease affects 1 in 10,000 males worldwide and results from deficiency of blood clotting factor VIII (FVIII). Both children and adults with hemophilia A (80 percent of all hemophilia) receive treatment that involves infusing FVIII protein into the bloodstream. However, about 30 percent of them develop an immune response in the form of antibodies to FVIII (inhibitors), rendering treatment ineffective and increasing risk of mortality.
For inhibitor-positive patients, immune tolerance induction (ITI) options are scarce, costly and invasive. Investigators at Indiana University School of Medicine, Children’s Hospital of Philadelphia and University of Pennsylvania joined efforts to explore immune responses to FVIII under an NIH-funded U54 initiative.
The study, led by IU School of Medicine’s Moanaro Biswas, PhD, and Valder R. Arruda, MD, PhD, from Children’s Hospital of Philadelphia and the University of Pennsylvania, is titled “B cell activating factor modulates the factor VIII immune response in hemophilia,” and was published in the Journal of Clinical Investigation earlier this month. Bhavya Doshi, MD, from Children’s Hospital of Philadelphia, is the first author.
In it, the group used plasma samples from pediatric and adult hemophilia A patients and animal models to determine whether BAFF plays a role in the generation and maintenance of FVIII inhibitors.
They also looked at combining antibody to BAFF in an ITI approach with a CD20 antibody (rituximab). Rituximab alone has shown mixed results in eradicating inhibitors when used alone in previous studies for hemophilia A.
Major findings from the study include:
- BAFF levels in plasma are higher in both pediatric and adult hemophilia A patients with persistent FVIII inhibitors, and correlate with FVIII antibody titers, suggesting that BAFF could be a potential harbinger for an ongoing humoral immune response to FVIII
- An increase in BAFF levels after rituximab-based therapy precludes tolerance to FVIII.
- Blocking BAFF is effective in the prevention of FVIII inhibitors in an animal model of hemophilia A.
- Combination CD20/BAFF monoclonal antibody therapy induces tolerance in a hemophilia A animal model with established FVIII inhibitors. This is due to a concerted effect of the combination therapy on memory B cells and plasma cells.
Next, the group will perform in-depth mechanistic studies to identify additional BAFF modifiers, which may provide additional insight into the pathways that lead to BAFF elevation and inhibitor formation.
These data also have important translational potential for inhibitor in hemophilia A, since there is an FDA-approved anti-BAFF antibody currently used as part of immunosuppressive regimens for autoimmune diseases.
Study co-authors are Jyoti Rana, PhD; Giancarlo Castaman, MD, PhD; Mostafa A. Shaheen, BA; Radoslaw Kaczmarek, PhD; John S. Butterfield, BS; Shannon L. Meeks, MD; and Cindy Leissinger, MD.
The study includes contributions from the Herman B Wells Center for Pediatric Research, IU School of Medicine; Perelman School of Medicine, University of Pennsylvania; Center for Bleeding Disorders and Coagulation, Careggi University Hospital; Aflac Cancer Center and Blood Disorders Center at Children’s Healthcare of Atlanta, Emory School of Medicine; Tulane University School of Medicine and Children’s Hospital of Philadelphia.
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