Minnesota, United States of America.
* Corresponding Author
GSC Advanced Research and Reviews, 2026, 28(02), 131–137
Article DOI: 10.30574/gscarr.2026.28.2.0206
Received on 12 July 2026; revised on 22 August 2026; accepted on 24 August 2026
Sepsis triggers a powerful hyper-inflammatory response intended to eliminate infection, but this immune
overactivation can lead to life-threatening organ failure. Efforts to control inflammation frequently raise the risk of secondary infections, presenting a major therapeutic challenge. IgE-antigen complexes (IgE-ACs) have emerged as a potential solution by engaging CD23 receptors on multiple immune cell types—including M2 macrophages, B cells, dendritic cells, and monocytes—to rebalance the immune system. This targeted immunotherapy can suppress harmful hyper-inflammation, promote tissue repair, and enhance protection against secondary infections. By fine-tuning both innate and adaptive responses, IgE-ACs offer a promising approach for restoring immune equilibrium and improving outcomes in sepsis. This review examines the underlying mechanisms, current evidence, and clinical potential of IgEACs, and discusses a prophetic example to illustrate the opportunities and hurdles of this innovative strategy.
Sepsis; Ige-Antigen Complexes (Ige-Acs); Hyper-Inflammation; CD23; Secondary Infections;
Immunotherapy
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Michael John Dochniak. IGE-ANTIGEN COMPLEXES (IGE-ACS) IN SEPSIS: PRECISION IMMUNOTHERAPY FOR IMMUNE BALANCE AND INFECTION CONTROL. GSC Advanced Research and Reviews, 2026, 28(02), 131–137. Article DOI: https://doi.org/10.30574/gscarr.2026.28.2.0206.