{"title":"PDE4抑制剂在银屑病治疗中的应用:目前的见解和未来的方向","authors":"Amit Sharma, Niyati Pandoh, Keerti Dayal, Aditya Raj, Kirandeep Kaur, Navjot Kaur Sandhu, Vineet Kumar Rai, Shubham Thakur, Balak Das Kurmi","doi":"10.1007/s10787-025-01778-y","DOIUrl":null,"url":null,"abstract":"<p><p>The chronic autoimmune disease known as psoriasis creates major life-quality problems for affected patients. The disease evolves through genetic and environmental triggers that trigger continuous keratinocyte multiplication with persistent inflammation. Research into psoriasis treatment now emphasizes phosphodiesterase-4 (PDE4) inhibitors because they manage cyclic adenosine monophosphate (cAMP) signaling to reduce inflammatory cytokine production. This review examines the PDE4 inhibitor potential for psoriasis treatment through investigation of their therapeutic functions alongside their mechanism of action and clinical response, safety data, and novel treatment approaches. The review gathered detailed information about clinical research and pharmaceutical operations of PDE4 inhibitors, specifically for apremilast, roflumilast, and crisaborole. This review also analyzes experimental PDE4 inhibitors alongside the advantages that appear when combining these drugs with biologics or phototherapy, together with methotrexate. The administration of PDE4 inhibitors creates higher intracellular cAMP levels that decrease TNF-α and IL-17 production as pro-inflammatory cytokines. The research on Apremilast, as the most prominent oral PDE4 inhibitor, shows that it both improves PASI scores and maintains good safety results. These medications treat psoriasis symptoms specifically through creams and gels, thus reducing the risk of whole-body side effects. The combined administration of PDE4 inhibitors and biologics leads to better therapeutic effects, which may lower both drug resistance rates and side effects. PDE4 inhibitors function as a valuable alternative therapeutic approach to both standard immunosuppressants and biologic medications in psoriasis treatment. New drug dosage methods connected to personalized treatment plans have the potential to raise patient care effectiveness. Researchers need to study ways to improve PDE4 inhibitor formulations, along with developing new combination therapy approaches to enhance sustained psoriasis disease treatment.</p>","PeriodicalId":13551,"journal":{"name":"Inflammopharmacology","volume":" ","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PDE4 inhibitors in psoriasis therapy: current insights and future directions.\",\"authors\":\"Amit Sharma, Niyati Pandoh, Keerti Dayal, Aditya Raj, Kirandeep Kaur, Navjot Kaur Sandhu, Vineet Kumar Rai, Shubham Thakur, Balak Das Kurmi\",\"doi\":\"10.1007/s10787-025-01778-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The chronic autoimmune disease known as psoriasis creates major life-quality problems for affected patients. The disease evolves through genetic and environmental triggers that trigger continuous keratinocyte multiplication with persistent inflammation. Research into psoriasis treatment now emphasizes phosphodiesterase-4 (PDE4) inhibitors because they manage cyclic adenosine monophosphate (cAMP) signaling to reduce inflammatory cytokine production. This review examines the PDE4 inhibitor potential for psoriasis treatment through investigation of their therapeutic functions alongside their mechanism of action and clinical response, safety data, and novel treatment approaches. The review gathered detailed information about clinical research and pharmaceutical operations of PDE4 inhibitors, specifically for apremilast, roflumilast, and crisaborole. This review also analyzes experimental PDE4 inhibitors alongside the advantages that appear when combining these drugs with biologics or phototherapy, together with methotrexate. The administration of PDE4 inhibitors creates higher intracellular cAMP levels that decrease TNF-α and IL-17 production as pro-inflammatory cytokines. The research on Apremilast, as the most prominent oral PDE4 inhibitor, shows that it both improves PASI scores and maintains good safety results. These medications treat psoriasis symptoms specifically through creams and gels, thus reducing the risk of whole-body side effects. The combined administration of PDE4 inhibitors and biologics leads to better therapeutic effects, which may lower both drug resistance rates and side effects. PDE4 inhibitors function as a valuable alternative therapeutic approach to both standard immunosuppressants and biologic medications in psoriasis treatment. New drug dosage methods connected to personalized treatment plans have the potential to raise patient care effectiveness. Researchers need to study ways to improve PDE4 inhibitor formulations, along with developing new combination therapy approaches to enhance sustained psoriasis disease treatment.</p>\",\"PeriodicalId\":13551,\"journal\":{\"name\":\"Inflammopharmacology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inflammopharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10787-025-01778-y\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inflammopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10787-025-01778-y","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
PDE4 inhibitors in psoriasis therapy: current insights and future directions.
The chronic autoimmune disease known as psoriasis creates major life-quality problems for affected patients. The disease evolves through genetic and environmental triggers that trigger continuous keratinocyte multiplication with persistent inflammation. Research into psoriasis treatment now emphasizes phosphodiesterase-4 (PDE4) inhibitors because they manage cyclic adenosine monophosphate (cAMP) signaling to reduce inflammatory cytokine production. This review examines the PDE4 inhibitor potential for psoriasis treatment through investigation of their therapeutic functions alongside their mechanism of action and clinical response, safety data, and novel treatment approaches. The review gathered detailed information about clinical research and pharmaceutical operations of PDE4 inhibitors, specifically for apremilast, roflumilast, and crisaborole. This review also analyzes experimental PDE4 inhibitors alongside the advantages that appear when combining these drugs with biologics or phototherapy, together with methotrexate. The administration of PDE4 inhibitors creates higher intracellular cAMP levels that decrease TNF-α and IL-17 production as pro-inflammatory cytokines. The research on Apremilast, as the most prominent oral PDE4 inhibitor, shows that it both improves PASI scores and maintains good safety results. These medications treat psoriasis symptoms specifically through creams and gels, thus reducing the risk of whole-body side effects. The combined administration of PDE4 inhibitors and biologics leads to better therapeutic effects, which may lower both drug resistance rates and side effects. PDE4 inhibitors function as a valuable alternative therapeutic approach to both standard immunosuppressants and biologic medications in psoriasis treatment. New drug dosage methods connected to personalized treatment plans have the potential to raise patient care effectiveness. Researchers need to study ways to improve PDE4 inhibitor formulations, along with developing new combination therapy approaches to enhance sustained psoriasis disease treatment.
期刊介绍:
Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas:
-Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states
-Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs
-Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents
-Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain
-Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs
-Muscle-immune interactions during inflammation [...]