识别、治疗和预防水痘感染的进展

C. Tyler Pitcock, Nicholas Van Sickels, Frank Romanelli
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引用次数: 0

摘要

背景猴痘(mpox)于 1958 年首次被分离出来,此后仅有零星的人类病例报告。猴痘病毒是一种双链 DNA 痘病毒,属于正痘病毒属,其天然动物库为小型啮齿类动物。该病毒分为 I 支系和 II 支系,其中 II 支系又分为 IIa 和 IIb。最常见的传播途径是通过大量呼吸道飞沫或与传染性病灶的皮肤接触。感染通常分为三个不同的阶段(潜伏期、前驱期和皮疹期),病程持续 2 到 4 周。淋巴腺肿大通常是一个显著的发现。目的在美国及其他地区出现和再次出现的猴痘感染凸显了对传播模式、临床表现、治疗和预防策略持续认识的必要性。结果2022年,在时隔几十年之后,美国再次出现猴痘病例,与欧洲报道的男男性行为者中爆发的猴痘病例不谋而合。2022 年的疫情以皮疹模式为特征,皮损通常集中在生殖器和肛周区域。疾病的临床过程可能因原有的免疫力低下(包括人类免疫缺陷病毒感染)而变得复杂。尽管目前尚无食品和药物管理局批准的麻风腮治疗方法,但已有包括替考韦利马特在内的一些抗病毒药物可供选择。其他研究较少但前景看好的替代品包括布林昔多福韦和疫苗免疫球蛋白静脉注射。结论 2022 年出现新的麻风腮感染病例,2023 年出现持续感染病例,这突出表明有必要继续对这种疾病和其他人畜共患病保持警惕。
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Advances in recognizing, treating, and preventing mpox infection

Background

Monkeypox (mpox) was first isolated in 1958, and since that time, only sporadic human cases have been reported. Mpox is a double-stranded DNA poxvirus of the Orthopox genus whose natural animal reservoir is small rodents. Classification of the virus is divided into clades I and II, with clade II being further subdivided into IIa and IIb. Transmission is most often accomplished through large respiratory droplets or skin-to-skin contact with infectious lesions. Infection typically proceeds in 3 distinct phases (incubation, prodrome, and rash), with the course of the illness extending 2 to 4 weeks. Lymphadenopathy is often a distinguishing finding.

Objective

The emergence and re-emergence of mpox infections in the United States and beyond have underscored the need for continued awareness of transmission patterns, clinical presentation, treatment, and preventative strategies.

Methods

A literature search was conducted for published literature using the keywords "Mpox", "Monkeypox" or "Monkeypox virus", between 1950 and 2023. All manuscript types were included and reviewed for relevant information related to Money pox and its management.

Results

In 2022 and after a span of decades, mpox cases re-emerged in the United States coinciding with reported outbreaks in Europe among men who have sex with men. The 2022 outbreak was distinguished by a pattern of rash where lesions were very commonly sequestered to genital and perianal regions. The clinical course of disease can be complicated by pre-existing immunocompromise including human immunodeficiency virus infection. Although no Food and Drug Administration–approved treatment for mpox exists, some antiviral options are available including tecovirimat. Other less studied but promising alternatives include brincidofovir and vaccinia immune globulin intravenous. Currently, 2 vaccine products are available for the prevention of mpox infection.

Conclusion

The appearance of new mpox infections in 2022 and lingering cases in 2023 underscore the need for continued vigilance against this and other zoonotic disease.

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