Autoimmune therapies targeting costimulation and emerging trends in multivalent therapeutics

Author:

Chittasupho Chuda12,Siahaan Teruna J1,Vines Charlotte M3,Berkland Cory14

Affiliation:

1. Department of Pharmaceutical Chemistry, University of Kansas, KS, USA.

2. Department of Pharmaceutical Technology, Srinakharinwirot University, Nakhonnayok, Thailand

3. Department of Microbiology, Molecular Genetics & Immunology, University of Kansas Medical Center, KS, USA

4. Department of Pharmaceutical Chemistry, Department of Chemical & Petroleum Engineering, 2030 Becker Drive, Lawrence, KS 66047, USA

Abstract

Proteins participating in immunological signaling have emerged as important targets for controlling the immune response. A multitude of receptor–ligand pairs that regulate signaling pathways of the immune response have been identified. In the complex milieu of immune signaling, therapeutic agents targeting mediators of cellular signaling often either activate an inflammatory immune response or induce tolerance. This review is primarily focused on therapeutics that inhibit the inflammatory immune response by targeting membrane-bound proteins regulating costimulation or mediating immune-cell adhesion. Many of these signals participate in larger, organized structures such as the immunological synapse. Receptor clustering and arrangement into organized structures is also reviewed and emerging trends implicating a potential role for multivalent therapeutics is posited.

Publisher

Future Science Ltd

Subject

Pharmaceutical Science

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