针对猴痘的诊断、生物标志物鉴定和药物发现的当前趋势

Pervej Alom Barbhuiya , Moksood Ahmed Laskar , Smitakshi Talukdar , Punam Kumari , Manash Pratim Pathak
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摘要

猴痘病毒是被称为猴痘(Mpox)的人畜共患疾病的病因,猴痘最近已广泛流行并引起了全世界的兴趣。两个主要的病毒分支引起麻疹:分支I,以前被称为中非分支;分支II,曾经被称为西非分支,包含亚分支IIa和IIb。这篇综述的重点是针对病毒生命周期的几个阶段,包括入侵、复制和组装的抗病毒治疗。它试图阐明重要的生物标志物,诊断方法和Mpox药物开发。m痘的生物学特性显示出其独特的特征:它是一种巨大的包膜DNA病毒,在感染细胞的细胞质中繁殖。不同的传播途径,包括呼吸道飞沫和与病变直接接触,都与麻疹的病理生理有关。发热、淋巴结肿大和皮疹是最初的症状,随后发展为丘疹、囊泡和脓疱。除了针对耐药菌株的KAY-2-41等新开发的选择外,正在研究西多福韦及其衍生物brincidofovir等现有抗病毒药物。MVA BN是世卫组织批准用于预防m痘病毒的一种新开发的疫苗,据报告约为。80 %有效。未来的研究应该集中在这些领域,同时更好地了解痘病毒与宿主的相互作用。全面的长期战略,包括疫苗接种、强有力的监测和治疗方案的持续创新,对于控制麻疹疫情和减轻未来的健康风险至关重要。这一全面分析强调,迫切需要持续监测、改进诊断技术和创造性治疗方法,以减轻潜在麻疹疫情的影响
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current trends in diagnostics, biomarker identification, and drug discovery targeting Monkeypox (Mpox)
The monkeypox virus is the cause of the zoonotic disease known as monkeypox (Mpox), which has recently become widely prevalent and attracted interest from across the world. Two main viral clades cause mpox: Clade I, which was previously known as the Central African clade, and Clade II, which was once known as the West African clade and contains the subclades IIa and IIb. The review focuses on antiviral treatments that target several stages of the viral lifecycle, including invasion, replication, and assembly. It attempts to elucidate the significant biomarkers, diagnostic methodologies, and Mpox drug development. The biology of mpox demonstrates its distinct features: it is a big, enveloped DNA virus that multiplies in the cytoplasm of infected cells. Different routes of transmission, including as respiratory droplets and direct contact with lesions, are involved in the pathophysiology of Mpox. Fever, lymphadenopathy, and rash are the first signs, which develop into papules, vesicles, and pustules. In addition to newly developed options like KAY-2–41 for resistant strains, established antiviral medications like cidofovir and its derivative brincidofovir are being investigated. MVA BN is a newly developed vaccine approved by WHO for use against Mpox virus and is reported to be approx. 80 % effective. Future research should focus on these areas, along with a better understanding of Mpox virus-host interactions. Comprehensive, long-term strategies, including vaccination, robust surveillance, and continued innovation in therapeutic options, will be essential to control Mpox outbreaks and mitigate future health risks. This thorough analysis emphasizes the critical need for ongoing monitoring, improved diagnosis techniques, and creative treatment approaches to lessen the effects of a potential Mpox outbreak
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