Rehman Shafi
Department of Histopathology, Institute of Pathology and Diagnostic Medicine, Khyber Medical University, Peshawar, Pakistan.
Proc (Bayl Univ Med Cent). 2024 Jul 3;37(5):851-857. doi: 10.1080/08998280.2024.2372745. eCollection 2024.
In the aftermath of anthrax bioterrorism, the US military began its smallpox immunization program in 2002. Dryvax was superseded in 2008 by ACAM2000, a second-generation smallpox vaccine, after clinical trials demonstrated favorable outcomes. However, these trials focused on significant adverse effects and provided less specific classifications and descriptions of cutaneous eruptions. The purpose of this systematic review was to investigate the clinicopathological characteristics of skin lesions that emerged in US military personnel following the reinstatement of new smallpox immunizations.
PubMed, ScienceDirect, and Google Scholar were searched. The search was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, using appropriate keywords.
Of the 467 studies initially identified, 5 (1%) were analyzed, with a sample size of 15. There were 10 men and 4 women. The mean age of presentation was 24.3 years. The interval between inoculation and eruption was 15 days. The length of the eruption until clearance was 36.26 days. Grossly, most skin lesions were described as having papules (n = 9). Histological examination revealed vesicles with spongiotic dermatitis and eosinophils (n = 5) and a dermal hypersensitivity reaction with lymphocytic vasculitis (capillaritis) (n = 2). Definitive diagnoses included acral and vesiculopustular dermatosis (n = 7), generalized vaccinia (GV) (n = 1), and progressive vaccinia (n = 1). Concurrent or near-concurrent vaccination was administered (n = 12).
Although rare, clinically significant skin lesions can occur after ACAM2000 administration. A feared complication of progressive vaccinia has been reported; however, to determine its causal relationship, further clinical trials are required to provide universal guidelines.
在炭疽生物恐怖事件之后,美国军方于2002年启动了天花免疫计划。2008年,在临床试验显示出良好结果后,Dryvax被第二代天花疫苗ACAM2000所取代。然而,这些试验侧重于严重不良反应,对皮肤疹的具体分类和描述较少。本系统评价的目的是调查美国军事人员重新接种新型天花疫苗后出现的皮肤病变的临床病理特征。
检索了PubMed、ScienceDirect和谷歌学术。检索按照系统评价和Meta分析的首选报告项目(PRISMA)指南进行,使用了适当的关键词。
在最初确定的467项研究中,分析了5项(1%),样本量为15。其中男性10名,女性4名。出现症状的平均年龄为24.3岁。接种与出疹之间的间隔为15天。皮疹消退的时长为36.26天。大体上,大多数皮肤病变被描述为丘疹(n = 9)。组织学检查显示有海绵状皮炎和嗜酸性粒细胞的水疱(n = 5)以及伴有淋巴细胞性血管炎(毛细血管炎)的真皮超敏反应(n = 2)。明确诊断包括肢端和水疱脓疱性皮肤病(n = 7)、全身性牛痘(GV)(n = 1)和进行性牛痘(n = 1)。同时或近乎同时进行了疫苗接种(n = 12)。
尽管罕见,但接种ACAM2000后可能会出现具有临床意义的皮肤病变。已经报告了令人担忧的进行性牛痘并发症;然而,要确定其因果关系,还需要进一步的临床试验来提供通用指南。