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以严重和持久病程为特征的猴痘作为艾滋病定义性事件:临床、免疫学和病毒学意义。

Mpox as AIDS-defining event with a severe and protracted course: clinical, immunological, and virological implications.

机构信息

Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases, Lazzaro Spallanzani IRCCS, Rome, Italy.

Cellular Immunology and Pharmacology Laboratory, National Institute for Infectious Diseases, Lazzaro Spallanzani IRCCS, Rome, Italy.

出版信息

Lancet Infect Dis. 2024 Feb;24(2):e127-e135. doi: 10.1016/S1473-3099(23)00482-6. Epub 2023 Sep 28.

DOI:10.1016/S1473-3099(23)00482-6
PMID:37778364
Abstract

A 59-year-old treatment-naive patient with advanced HIV infection presented with a severe and protracted course of mpox (formerly known as monkeypox) that did not respond to the current mpox treatment options. The patient worsened clinically, and developed new mucocutaneous lesions and necrotic evolution of pre-existing ones, along with multiple bilateral lung nodules and the appearance of a tracheal necrotic lesion. Although severe forms of mpox have been observed in people with severe immune system deficiency, including those with advanced HIV presentation, the immunological mechanisms underlying this observation have not yet been fully explained. To our knowledge, this is the first account of a necrotising mpox in a person living with HIV, with viral shedding for more than 11 months and a comprehensive immunological description. Moreover, we documented the virus' persistence by detecting mpox virus DNA from multiple sites and quantified anti-monkeypox virus IgA, IgM, IgG, and neutralising antibodies in serum samples. The severe HIV-driven immune depression and the presence of other co-infections might skew and impair immune responses, thus contributing to the persistence of monkeypox virus infection. Further investigations of immune responses to monkeypox virus infection in people with severe immunosuppression are required to improve management and prevention.

摘要

一位 59 岁的初治 HIV 感染患者出现了严重且迁延不愈的猴痘(曾称为猴痘),目前的猴痘治疗方案对此无效。患者病情恶化,出现新的粘膜皮肤损伤和原有损伤的坏死进展,同时伴有多个双侧肺结节和气管坏死损伤。尽管在严重免疫功能缺陷人群中观察到了包括 HIV 晚期患者在内的严重猴痘病例,但这一观察结果的免疫学机制尚未得到充分解释。据我们所知,这是首例 HIV 感染者发生坏死性猴痘的报告,病毒脱落持续超过 11 个月,并对其进行了全面的免疫学描述。此外,我们通过从多个部位检测到猴痘病毒 DNA 并对血清样本中的抗猴痘病毒 IgA、IgM、IgG 和中和抗体进行定量,证明了病毒的持续存在。严重的 HIV 驱动的免疫抑制以及其他合并感染的存在可能会扭曲和损害免疫反应,从而导致猴痘病毒感染的持续存在。需要进一步研究严重免疫抑制人群对猴痘病毒感染的免疫反应,以改善管理和预防。

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