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Título

Unveiling the Multifaceted Roles of ISG15: From Immunomodulation to Therapeutic Frontiers

AutorÁlvarez, Enrique ; Falqui, Michela; Sin, Laura; McGrail, Joseph Patrick; Perdiguero, Beatriz; Coloma, Rocío; Marcos-Villar, Laura CSIC ORCID ; Tárrega, Céline; Esteban, Mariano CSIC ORCID ; Gómez, Carmen E. CSIC ORCID; Guerra, Susana
Palabras claveIFN
ISG15
ISGylation
Vaccines
Inflammation
Immunity
Adjuvant
Cytokines
Fecha de publicaciónfeb-2024
EditorMultidisciplinary Digital Publishing Institute
CitaciónVaccines 12(2): 153 (2024)
ResumenThe Interferon Stimulated Gene 15 (ISG15), a unique Ubiquitin-like (Ubl) modifier exclusive to vertebrates, plays a crucial role in the immune system. Primarily induced by interferon (IFN) type I, ISG15 functions through diverse mechanisms: (i) covalent protein modification (ISGylation); (ii) non-covalent intracellular action; and (iii) exerting extracellular cytokine activity. These various roles highlight its versatility in influencing numerous cellular pathways, encompassing DNA damage response, autophagy, antiviral response, and cancer-related processes, among others. The well-established antiviral effects of ISGylation contrast with its intriguing dual role in cancer, exhibiting both suppressive and promoting effects depending on the tumour type. The multifaceted functions of ISG15 extend beyond intracellular processes to extracellular cytokine signalling, influencing immune response, chemotaxis, and anti-tumour effects. Moreover, ISG15 emerges as a promising adjuvant in vaccine development, enhancing immune responses against viral antigens and demonstrating efficacy in cancer models. As a therapeutic target in cancer treatment, ISG15 exhibits a double-edged nature, promoting or suppressing oncogenesis depending on the tumour context. This review aims to contribute to future studies exploring the role of ISG15 in immune modulation and cancer therapy, potentially paving the way for the development of novel therapeutic interventions, vaccine development, and precision medicine.
Versión del editorhttps://doi.org/10.3390/vaccines12020153
URIhttp://hdl.handle.net/10261/345235
DOI10.3390/vaccines12020153
E-ISSN2076-393X
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