Therapeutic Advances in Psoriasis: From Biologics to Emerging Oral Small Molecules.

IF 3 Q3 IMMUNOLOGY Antibodies Pub Date : 2024-09-14 DOI:10.3390/antib13030076
Francesco Ferrara, Chiara Verduci, Emanuela Laconi, Andrea Mangione, Chiara Dondi, Marta Del Vecchio, Veronica Carlevatti, Andrea Zovi, Maurizio Capuozzo, Roberto Langella
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Abstract

Psoriasis is a persistent, inflammatory condition affecting millions globally, marked by excessive keratinocyte proliferation, immune cell infiltration, and widespread inflammation. Over the years, therapeutic approaches have developed significantly, shifting from conventional topical treatments and phototherapy to more sophisticated systemic interventions such as biologics and, recently, oral small-molecule drugs. This review seeks to present a comprehensive investigation of the existing psoriasis treatment options, focusing on biologic agents, oral small molecules, and emerging treatments. Several categories of biologic treatments have received regulatory approval for psoriasis, including TNF-α, IL-17, IL-12/23, and IL-23 inhibitors. Biologics have revolutionized the treatment of psoriasis. These targeted therapies offer significant improvement in disease control and quality of life, with acceptable safety profiles. However, limitations such as cost, potential immunogenicity, and administration challenges have driven the exploration of alternative treatment modalities. Oral small molecules, particularly inhibitors of Janus kinase (JAK), have emerged as options due to their convenience and efficacy. These agents represent a paradigm shift in the management of the condition, offering oral administration and targeted action on specific signaling pathways. In addition to existing therapies, the review explores emerging treatments that hold promise for the future of psoriasis care. These include innovative small-molecule inhibitors. Early-stage clinical trials suggest these agents may enhance outcomes for psoriasis patients. In conclusion, the therapeutic landscape of psoriasis is rapidly evolving, emphasizing targeted, patient-centered treatments. Ongoing research and development are expected to lead to more personalized and effective management strategies for this complex condition.

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银屑病的治疗进展:从生物制剂到新兴口服小分子药物。
银屑病是一种顽固性炎症,影响着全球数百万人,其特征是角质细胞过度增殖、免疫细胞浸润和广泛的炎症。多年来,治疗方法有了长足的发展,从传统的局部治疗和光疗转变为更复杂的系统干预,如生物制剂和最近的口服小分子药物。本综述旨在全面研究现有的银屑病治疗方案,重点关注生物制剂、口服小分子药物和新兴疗法。有几类生物制剂已获得银屑病监管部门的批准,包括 TNF-α、IL-17、IL-12/23 和 IL-23 抑制剂。生物制剂彻底改变了银屑病的治疗方法。这些靶向疗法可显著改善疾病控制和生活质量,安全性也可接受。然而,成本、潜在的免疫原性和用药挑战等限制因素促使人们探索其他治疗方法。口服小分子药物,尤其是 Janus 激酶(JAK)抑制剂,因其使用方便和疗效显著而成为一种选择。这些药物口服给药,并能对特定信号通路产生靶向作用,代表了该病治疗模式的转变。除现有疗法外,本综述还探讨了未来有望用于银屑病治疗的新兴疗法。其中包括创新的小分子抑制剂。早期临床试验表明,这些药物可提高银屑病患者的治疗效果。总之,银屑病的治疗格局正在迅速演变,强调有针对性的、以患者为中心的治疗。正在进行的研究和开发有望为这种复杂的疾病带来更加个性化和有效的治疗策略。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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