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皮肤和黏膜利什曼病:新兴疗法和疾病管理进展。

Cutaneous and mucocutaneous leishmaniasis: emerging therapies and progress in disease management.

机构信息

Royal Free Hospital, Dermatology Department, London, NW3 2QG, UK.

出版信息

Expert Opin Pharmacother. 2010 Mar;11(4):557-69. doi: 10.1517/14656560903555219.


DOI:10.1517/14656560903555219
PMID:20163267
Abstract

IMPORTANCE OF THE FIELD: Cutaneous leishmaniasis (CL) is a major tropical skin disease. Its incidence continues to increase, and disease control and management are challenging. Available therapies remain inadequate and are associated with low efficacy, toxicity, difficulties with administration, or are expensive. AREAS COVERED IN THIS REVIEW: This article describes progress in the therapeutics of CL since 2006. Clinical trials have provided further evidence for the use of alternative systemic agents to first-line antimonials, an enhanced topical paromomycin preparation, the efficacy of thermotherapy, photodynamic therapy as an emerging physical therapy, and the role of immunotherapy and immunomodulators as adjuncts to chemotherapy. In addition, in vitro studies have demonstrated the anti-leishmanial effects of several drugs, which might represent potential future therapeutic agents for CL. WHAT THE READER WILL GAIN: An overview of the magnitude and complexity of this heterogenous disease, and an update on recent advances in therapeutics and future directions for new drug development. TAKE HOME MESSAGE: Drug therapy for CL must be tailored according to infective species, endemic region, and host responses; a range of different therapies and modalities is therefore required. The impetus for new drug development must continue, combination therapies need to be evaluated, and robust and comparative trials of existing agents are required to adequately assess their efficacy and tolerability.

摘要

重要性领域:皮肤利什曼病(CL)是一种主要的热带皮肤疾病。其发病率持续上升,疾病的控制和管理具有挑战性。现有的治疗方法仍然不足,且疗效低、毒性大、给药困难或昂贵。

这篇综述涵盖了自 2006 年以来 CL 治疗方面的进展。临床试验为替代一线锑剂的替代全身药物、增强的局部巴龙霉素制剂、热疗的疗效、作为新兴物理疗法的光动力疗法以及免疫疗法和免疫调节剂作为化疗辅助剂的疗效提供了进一步的证据。此外,体外研究表明,几种药物具有抗利什曼原虫作用,它们可能成为 CL 的潜在未来治疗药物。

读者将获得:对这种异质性疾病的严重程度和复杂性的概述,以及对治疗学最新进展和新药开发未来方向的更新。

重要信息:CL 的药物治疗必须根据感染物种、流行地区和宿主反应进行调整;因此需要多种不同的治疗方法和方式。必须继续推动新药的开发,需要评估联合治疗,并对现有药物进行强有力的和有比较的试验,以充分评估其疗效和耐受性。

相似文献

[1]
Cutaneous and mucocutaneous leishmaniasis: emerging therapies and progress in disease management.

Expert Opin Pharmacother. 2010-3

[2]
[Development of antituberculous drugs: current status and future prospects].

Kekkaku. 2006-12

[3]
[Diagnosis and therapy of cutaneous and mucocutaneous Leishmaniasis in Germany].

J Dtsch Dermatol Ges. 2011-11

[4]
Therapeutic options for old world cutaneous leishmaniasis and new world cutaneous and mucocutaneous leishmaniasis.

Drugs. 2013-11

[5]
[Management of cutaneous leishmaniasis in adults and children].

Med Trop (Mars). 2005-11

[6]
A Therapeutic update on Cutaneous leishmaniasis.

J Coll Physicians Surg Pak. 2003-8

[7]
Cutaneous and mucocutaneous leishmaniasis.

Infect Dis Clin North Am. 2012-4-17

[8]
Leishmaniases and HIV/AIDS co-infections: review of common features and management experiences.

Ethiop Med J. 2002-4

[9]
Cutaneous leishmaniasis: advances in disease pathogenesis, diagnostics and therapeutics.

Clin Exp Dermatol. 2010-10

[10]
[Treatment of cutaneous leishmaniasis--an update].

Harefuah. 2002-1

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[1]
Photodynamic therapy in management of cutaneous leishmaniasis: A systematic review.

Lasers Med Sci. 2024-8-29

[2]
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Pharmaceutics. 2023-4-6

[3]
Natural Occurrence in Venomous Arthropods of Antimicrobial Peptides Active against Protozoan Parasites.

Toxins (Basel). 2019-9-25

[4]
Imported cutaneous leishmaniasis caused by Leishmania major in a Chinese laborer who worked in Saudi Arabia.

An Bras Dermatol. 2016

[5]
Novel low-cost thermotherapy for cutaneous leishmaniasis in Peru.

PLoS Negl Trop Dis. 2013-5-2

[6]
Miltefosine-induced apoptotic cell death on Leishmania major and L. tropica strains.

Korean J Parasitol. 2011-3

[7]
Δ²,³-ivermectin ethyl secoester, a conjugated ivermectin derivative with leishmanicidal activity but without inhibitory effect on mammalian P-type ATPases.

Naunyn Schmiedebergs Arch Pharmacol. 2010-11-19

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