原生动物感染治疗的最新进展。

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2011-01-01 Epub Date: 2011-03-09 DOI:10.2174/1874104501105010004
Mario Zucca, Dianella Savoia
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引用次数: 36

摘要

原生动物寄生虫引起严重的人类和人畜共患感染,包括威胁生命的疾病,如疟疾、非洲和美洲锥虫病以及利什曼病。这些疾病在发达国家已不再常见,但它们加在一起仍威胁着约40%的世界人口(世卫组织估计)。发展中国家的死亡率和发病率很高,缺乏疫苗使得化疗成为唯一合适的选择。然而,现有的抗寄生虫药物因或多或少明显的毒副作用和耐药性的出现而受到阻碍。由于寄生虫病的主要流行地区是世界上最贫穷的地区,制药公司对开发新药的兴趣历来很少。以热带病为重点的公私伙伴关系的建立正在改变这种情况,使人们能够利用过去十年中在基因组学、蛋白质组学和计算机药物发现方法方面取得的技术进步。这些技术允许鉴定在某些情况下由不同寄生虫共有的新分子靶点。本文综述了近年来在蛋白酶和拓扑异构酶抑制剂、抗菌肽和细胞穿透肽、RNA干扰等领域的研究进展。我们还报道了快速发展的新载体领域(微纳米颗粒,介孔材料),在某些情况下,它们可以跨越宿主或寄生虫的天然屏障,并通过选择性地将新的或已经在使用的药物递送到靶点,最大限度地减少剂量和副作用。
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Current developments in the therapy of protozoan infections.

Protozoan parasites cause serious human and zoonotic infections, including life-threatening diseases such as malaria, African and American trypanosomiasis, and leishmaniasis. These diseases are no more common in the developed world, but together they still threaten about 40% of the world population (WHO estimates). Mortality and morbidity are high in developing countries, and the lack of vaccines makes chemotherapy the only suitable option. However, available antiparasitic drugs are hampered by more or less marked toxic side effects and by the emergence of drug resistance. As the main prevalence of parasitic diseases occurs in the poorest areas of the world, the interest of the pharmaceutical companies in the development of new drugs has been traditionally scarce. The establishment of public-private partnerships focused on tropical diseases is changing this situation, allowing the exploitation of the technological advances that took place during the past decade related to genomics, proteomics, and in silico drug discovery approaches. These techniques allowed the identification of new molecular targets that in some cases are shared by different parasites. In this review we outline the recent developments in the fields of protease and topoisomerase inhibitors, antimicrobial and cell-penetrating peptides, and RNA interference. We also report on the rapidly developing field of new vectors (micro and nano particles, mesoporous materials) that in some cases can cross host or parasite natural barriers and, by selectively delivering new or already in use drugs to the target site, minimize dosage and side effects.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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