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      Next Generation PDE4 Inhibitors that Selectively Target PDE4B/D Subtypes: A Narrative Review

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          Abstract

          For decades, topical corticosteroids have been the mainstay of treatment for mild-to-moderate inflammatory skin diseases, even though only short-term use is approved for these agents and systemic inflammation is not addressed. Increased understanding of the immunopathogenesis of these conditions, especially for psoriasis and atopic dermatitis, has facilitated the development of antibody-based drugs that neutralize single key cytokines or their associated receptors, such as interleukin (IL)-17A/F, IL-23, and IL-17RA in psoriasis and IL-13 and IL-4Rα in atopic dermatitis. However, oral therapy is still preferred by many patients owing to the ease of use and needle-free administration. Phosphodiesterase 4 (PDE4) inhibitors have been approved for both oral and topical use for inflammatory skin diseases. In this review, we present a summary of an emerging class of selective PDE4B/D inhibitors under clinical development and compare the differences in selectivity of this new generation of PDE4 inhibitors with the less selective currently approved PDE4 inhibitors.

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          Most cited references27

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          Apremilast, an oral phosphodiesterase 4 (PDE4) inhibitor, in patients with moderate to severe plaque psoriasis: Results of a phase III, randomized, controlled trial (Efficacy and Safety Trial Evaluating the Effects of Apremilast in Psoriasis [ESTEEM] 1).

          Apremilast works intracellularly to regulate inflammatory mediators.
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            Apremilast is a selective PDE4 inhibitor with regulatory effects on innate immunity.

            Apremilast, an oral small molecule inhibitor of phosphodiesterase 4 (PDE4), is in development for chronic inflammatory disorders, and has shown efficacy in psoriasis, psoriatic arthropathies, and Behçet's syndrome. In March 2014, the US Food and Drug Administration approved apremilast for the treatment of adult patients with active psoriatic arthritis. The properties of apremilast were evaluated to determine its specificity, effects on intracellular signaling, gene and protein expression, and in vivo pharmacology using models of innate and adaptive immunity. Apremilast inhibited PDE4 isoforms from all four sub-families (A1A, B1, B2, C1, and D2), with IC50 values in the range of 10 to 100 nM. Apremilast did not significantly inhibit other PDEs, kinases, enzymes, or receptors. While both apremilast and thalidomide share a phthalimide ring structure, apremilast lacks the glutarimide ring and thus fails to bind to cereblon, the target of thalidomide action. In monocytes and T cells, apremilast elevated intracellular cAMP and induced phosphorylation of the protein kinase A substrates CREB and activating transcription factor-1 while inhibiting NF-κB transcriptional activity, resulting in both up- and down-regulation of several genes induced via TLR4. Apremilast reduced interferon-α production by plasmacytoid dendritic cells and inhibited T-cell cytokine production, but had little effect on B-cell immunoglobulin secretion. In a transgenic T-cell and B-cell transfer murine model, apremilast (5mg/kg/day p.o.) did not affect clonal expansion of either T or B cells and had little or no effect on their expression of activation markers. The effect of apremilast on innate immunity was tested in the ferret lung neutrophilia model, which allows monitoring of the known PDE4 inhibitor gastrointestinal side effects (nausea and vomiting). Apremilast significantly inhibited lung neutrophilia at 1mg/kg, but did not induce significant emetic reflexes at doses <30 mg/kg. Overall, the pharmacological effects of apremilast are consistent with those of a targeted PDE4 inhibitor, with selective effects on innate immune responses and a wide therapeutic index compared to its gastrointestinal side effects.
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              Efficacy and safety of apremilast, an oral phosphodiesterase 4 inhibitor, in patients with moderate-to-severe plaque psoriasis over 52 weeks: a phase III, randomized controlled trial (ESTEEM 2).

              Apremilast, an oral phosphodiesterase 4 inhibitor, regulates immune responses associated with psoriasis.
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                Author and article information

                Contributors
                ablauvelt@oregonmedicalresearch.com
                Journal
                Dermatol Ther (Heidelb)
                Dermatol Ther (Heidelb)
                Dermatology and Therapy
                Springer Healthcare (Cheshire )
                2193-8210
                2190-9172
                4 November 2023
                4 November 2023
                December 2023
                : 13
                : 12
                : 3031-3042
                Affiliations
                [1 ]Oregon Medical Research Center, ( https://ror.org/03m027021) 9495 SW Locust Street, Suite G, Portland, OR 97223 USA
                [2 ]GRID grid.55602.34, ISNI 0000 0004 1936 8200, Division of Clinical Dermatology and Cutaneous Science, Department of Medicine, , Dalhousie University and Nova Scotia Health, ; Halifax, Canada
                [3 ]Froedtert Hospital and the Medical College of Wisconsin, ( https://ror.org/01nhrc260) Milwaukee, WI USA
                [4 ]George Washington University School of Medicine and Health Sciences, ( https://ror.org/00y4zzh67) Washington, DC USA
                [5 ]GRID grid.6936.a, ISNI 0000000123222966, Technical University of Munich, ; Munich, Germany
                [6 ]Department of Medicine Solna, Karolinska Institutet, ( https://ror.org/056d84691) Stockholm, Sweden
                [7 ]UNION Therapeutics A/S, Hellerup, Denmark
                [8 ]GRID grid.5170.3, ISNI 0000 0001 2181 8870, Novo Nordisk Foundation Center for Biosustainability, , Technical University of Denmark (DTU), ; Lyngby, Denmark
                [9 ]UNION Therapeutics A/S, Hellerup, Denmark
                [10 ]GRID grid.5379.8, ISNI 0000000121662407, Dermatology Centre, Salford Royal NHS Foundation Trust, Manchester NIHR Biomedical Research Centre, , The University of Manchester, ; Manchester, UK
                Author information
                http://orcid.org/0000-0002-2633-985X
                Article
                1054
                10.1007/s13555-023-01054-3
                10689637
                37924462
                9ea69910-6b01-4061-aae7-803e5f9044bf
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 18 August 2023
                : 2 October 2023
                Categories
                Review
                Custom metadata
                © Springer Healthcare Ltd., part of Springer Nature 2023

                Dermatology
                pde4 inhibitors,pde4b,pde4d,nerandomilast,orismilast,pf-07038124,zatolmilast
                Dermatology
                pde4 inhibitors, pde4b, pde4d, nerandomilast, orismilast, pf-07038124, zatolmilast

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