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Giornale Italiano di Dermatologia e Venereologia 2020 Oct 07

DOI: 10.23736/S0392-0488.20.06580-3

Copyright © 2020 EDIZIONI MINERVA MEDICA

lingua: Inglese

Candida infections in patients with psoriasis and psoriatic arthritis treated with interleukin-17 inhibitors and their practical management

Carmen RODRÍGUEZ-CERDEIRA1, 2, 3, 4, 5, 6 , José L. GONZÁLEZ-CESPÓN 1, Erick MARTÍNEZ-HERRERA 1, 3, 6, Miguel CARNERO-GREGORIO 1, 5, Adriana LÓPEZ-BARCENAS 3, 6, Alexey SERGEEV 3, 4, 5, 6, Ditte M. SAUNTE 4, 5, 8, 9

1 Efficiency, Quality, and Costs in Health Services Research Group (EFISALUD), Health Research Institute, SERGAS-VIGO, Vigo, Spain; 2 Department of Dermatology, Hospital Meixoeiro, University of Vigo, Vigo, Spain; 3 Ibero-Latin American College of Dermatology (CILAD), Buenos Aires, Argentina; 4 European Academy of Dermatology and Venereology (EADV), Lugano, Switzerland; 5 Department of Molecular Diagnosis, Institute of Cellular and Molecular Studies (ICM), Lugo, Spain; 6 Manuel Gea González General Hospital, Mexico City, Mexico; 7 Dmitrovskoe Central Research Dermatology Clinic, Moscow, Russia; 8 Department of Dermatology, Zealand University Hospital, Roskilde, Denmark; 9 Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark


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INTRODUCTION: Interleukin 17A (IL-17A) is a pro-inflammatory cytokine produced by helper T cells (Th17) and other cells of the immune system and exerts pleiotropic effects on multiple cell lines. The role of IL-17 in the pathogenesis of numerous inflammatory disorders is well-documented. IL-17 activates signalling through the IL-17 receptor, which induces other proinflammatory cytokines, antimicrobial peptides, and neutrophil chemokines that are important for antifungal activity.
EVIDENCE ACQUISITION: Healthy levels of IL-17 can protect the host against extracellular bacterial and fungal infections in mucous membranes and epithelia. IL-17 deficiency reduces control of certain infections, while excessive IL-17 can produce unwanted inflammatory effects.
EVIDENCE SYNTHESIS: Although the efficacy of the therapeutic blockade of this cytokine has been proven in several autoimmune diseases such as psoriasis and psoriatic arthritis, this strategy could also exacerbate fungal infections in such patients. Therefore, a better understanding of IL-17-mediated immunity to Candida is necessary for the development of autoimmune therapeutics that maintain antifungal immunity.
CONCLUSIONS: In this review, we include a study of the new anti-IL-17 biological agents (secukinumab, ixekizumab, and bromalizumab ) used for moderate-to-severe psoriasis and psoriatic arthritis treatment in clinical practice, as well as pivotal trials with bimekizumab. We study the relationship of these biological agents and the appearance of candidiasis in its various clinical forms.


KEY WORDS: Anti-IL-17; Psoriasis; Psoriatic arthritis; Candidiasis; Clinical practice

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