Rubén L Rodríguez-Expósito, Ines Sifaoui, María Reyes-Batlle, José E Piñero, Jacob Lorenzo-Morales
{"title":"An expert's guide to <i>Acanthamoeba</i> keratitis pharmacology.","authors":"Rubén L Rodríguez-Expósito, Ines Sifaoui, María Reyes-Batlle, José E Piñero, Jacob Lorenzo-Morales","doi":"10.1080/17512433.2026.2724060","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong><i>Acanthamoeba</i> keratitis (AK) is a rare but sight-threatening corneal infection, increasingly associated with contact lens wear, whose treatment remains constrained by the lack of agents that are both cysticidal and well tolerated by the cornea. This review appraises the current pharmacological landscape and the obstacles impeding therapeutic progress.</p><p><strong>Areas covered: </strong>PubMed, Scopus, Google Scholar, and Web of Science were searched for articles published between January 2000 and June 2026 using combinations of the terms '<i>Acanthamoeba</i> keratitis,' 'treatment,' 'pharmacology,' 'amoebicidal' and individual drug names; reference lists were hand-searched. We provide an overview of the epidemiology, biology, life cycle and pathogenic mechanisms of AK. We then critically evaluate current clinical management strategies and their inherent limitations before providing a comprehensive synthesis of recent <i>in vitro</i> and <i>in vivo</i> investigations to identify effective drugs that target both the cyst and trophozoite stages with low cytotoxicity.</p><p><strong>Expert opinion: </strong>Prolonged, intensive topical regimens impose a substantial burden that drives poor adherence and relapse, and standardized protocol-based dosing offers the most immediate practical gain. The field now requires agents combining potent cysticidal activity with corneal biocompatibility, alongside standardized assays and validated <i>ex vivo</i> models, so that promising laboratory activity translates into genuine clinical benefit.</p>","PeriodicalId":12207,"journal":{"name":"Expert Review of Clinical Pharmacology","volume":" ","pages":"795-806"},"PeriodicalIF":3.6000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert Review of Clinical Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17512433.2026.2724060","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/28 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Acanthamoeba keratitis (AK) is a rare but sight-threatening corneal infection, increasingly associated with contact lens wear, whose treatment remains constrained by the lack of agents that are both cysticidal and well tolerated by the cornea. This review appraises the current pharmacological landscape and the obstacles impeding therapeutic progress.
Areas covered: PubMed, Scopus, Google Scholar, and Web of Science were searched for articles published between January 2000 and June 2026 using combinations of the terms 'Acanthamoeba keratitis,' 'treatment,' 'pharmacology,' 'amoebicidal' and individual drug names; reference lists were hand-searched. We provide an overview of the epidemiology, biology, life cycle and pathogenic mechanisms of AK. We then critically evaluate current clinical management strategies and their inherent limitations before providing a comprehensive synthesis of recent in vitro and in vivo investigations to identify effective drugs that target both the cyst and trophozoite stages with low cytotoxicity.
Expert opinion: Prolonged, intensive topical regimens impose a substantial burden that drives poor adherence and relapse, and standardized protocol-based dosing offers the most immediate practical gain. The field now requires agents combining potent cysticidal activity with corneal biocompatibility, alongside standardized assays and validated ex vivo models, so that promising laboratory activity translates into genuine clinical benefit.
棘阿米巴角膜炎(AK)是一种罕见但威胁视力的角膜感染,越来越多地与隐形眼镜佩戴相关,其治疗仍然受到缺乏囊性和角膜耐受性良好的药物的限制。这篇综述评估了当前的药理学景观和阻碍治疗进展的障碍。检索领域:PubMed、Scopus、谷歌Scholar和Web of Science,检索2000年1月至2026年6月期间发表的文章,检索词包括“棘阿米巴角膜炎”、“治疗”、“药理学”、“阿米巴杀菌剂”和个别药物名称;参考书目是手工检索的。本文综述了AK的流行病学、生物学、生命周期和致病机制。然后,我们批判性地评估当前的临床管理策略及其固有的局限性,然后提供最近的体外和体内研究的综合,以确定针对囊肿和滋养体阶段的有效药物,同时具有低细胞毒性。专家意见:长期、强化的局部治疗方案带来了巨大的负担,导致依从性差和复发,而基于方案的标准化剂量提供了最直接的实际收益。该领域现在需要结合有效囊泡活性和角膜生物相容性的药物,以及标准化的分析和验证的离体模型,以便有希望的实验室活性转化为真正的临床效益。
期刊介绍:
Advances in drug development technologies are yielding innovative new therapies, from potentially lifesaving medicines to lifestyle products. In recent years, however, the cost of developing new drugs has soared, and concerns over drug resistance and pharmacoeconomics have come to the fore. Adverse reactions experienced at the clinical trial level serve as a constant reminder of the importance of rigorous safety and toxicity testing. Furthermore the advent of pharmacogenomics and ‘individualized’ approaches to therapy will demand a fresh approach to drug evaluation and healthcare delivery.
Clinical Pharmacology provides an essential role in integrating the expertise of all of the specialists and players who are active in meeting such challenges in modern biomedical practice.