Povetacicept (ALPN-303), a Potent Dual BAFF/APRIL Antagonist, Suppresses Disease in a Mouse Model of Autoimmune Encephalitis
Katherine Lewis1, Zahra Maria1, Luana Griffin1, Joel Lenox1, NingXin Wang1, Stacey Dillon1, Stanford Peng1
1Alpine Immune Sciences
Objective:

To explore the role of the BAFF and APRIL cytokines in the pathogenesis of anti-N-methyl-D-aspartate receptor (NMDAR) autoimmune encephalitis.

Background:

BAFF and APRIL are cytokines that signal through TACI, BCMA, and/or BAFF-R and play important roles in the activation, differentiation and/or survival of B cells, particularly antibody-secreting cells, as well as T cells and innate immune cells. Povetacicept is an Fc fusion protein of an engineered TACI domain which mediates significantly more potent dual inhibition of APRIL and BAFF than WT TACI-Fc, which has shown promise in the treatment of myasthenia gravis and other antibody-related diseases. Povetacicept may provide a more efficacious treatment option for autoimmune encephalitis and other antibody-related neurological diseases.

Design/Methods:

Mice (female C57BL/6NJ) were immunized every 4 weeks for a total of 3 immunizations with an encephalitogenic peptide (GluN1356-385) of the human/mouse NMDAR subunit. At the 2nd immunization, when high circulating levels of anti-GluN1 antibodies were detected, mice were placed into two treatment groups in a balanced manner, such that each had similar anti-GluN1 levels. Mice were treated 2x/week with povetacicept (10 mg/kg) or a molar-matched dose of Fc control over 5 weeks, then evaluated at Week 10 for anti-GluN1 titers and cerebral IgG deposits. Splenocytes were also evaluated by flow cytometry to track immune cell subsets important for antibody production.

Results:

Povetacicept treatment was associated with significantly lower serum anti-GluN1 antibodies (p=0.0003) and IgG deposition in brains (p=0.0009) than Fc control-treated mice. Moreover, total numbers of splenic B, germinal center, T follicular helper, and plasma cells were significantly lower in povetacicept-treated mice than Fc control-treated mice (p≤0.0003).

Conclusions:

Povetacicept demonstrates promising efficacy in a preclinical model of autoimmune encephalitis, reducing pathogenic autoantibodies and cerebral Ig deposition. Povetacicept may hold promise in the treatment of autoimmune encephalitis and other autoantibody-related neurological diseases.

10.1212/WNL.0000000000205254