Minnesota, United States of America.
* Corresponding Author
GSC Advanced Research and Reviews, 2026, 29(01), 209–215
Article DOI: 10.30574/gscarr.2026.29.1.0275
Received on 06 September 2026; revised on 12 October 2026; accepted on 14 October 2026
Giant cell myocarditis (GCM) is a rare, rapidly progressive cardiac disorder characterized by giant, multinucleated cells that contribute to severe myocardial damage. Existing combination immunosuppressive therapies, although directed at immune-mediated injury, lack precision and are associated with considerable adverse effects. A CD23-targeted intervention holds promise as a more selective, safer adjunctive treatment. This review evaluates a strategy centered on the low-affinity IgE receptor (CD23/FcεRII), predominantly expressed on alternatively activated (M2a) macrophages and B cells. The proposed method uses engineered anti-IgE–IgE complexes to engage CD23, inhibiting macrophage fusion—a defining feature of GCM—and fostering a more anti-inflammatory immune milieu. This therapy also aims to protect myocardial tissue by suppressing pathogenic T-cell responses and slowing disease progression. The review details the scientific basis for this approach, outlines laboratory testing protocols, suggests optimal delivery systems, and considers translational hurdles to clinical implementation.
Giant Cell Myocarditis, CD23, M2a Macrophages, Anti-IgE:IgE Complexes, Immunomodulation, Macrophage Fusion
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Michael John Dochniak. CD23-TARGETED IMMUNOTHERAPY FOR GIANT CELL MYOCARDITIS. GSC Advanced Research and Reviews, 2026, 29(01), 209–215. Article DOI: https://doi.org/10.30574/gscarr.2026.29.1.0275.