MMWR Morb Mortal Wkly Rep. 2022 Sep 9;71(36):1155-1158. doi: 10.15585/mmwr.mm7136e1.
Since May 2022, approximately 20,000 cases of monkeypox have been identified in the United States, part of a global outbreak occurring in approximately 90 countries and currently affecting primarily gay, bisexual, and other men who have sex with men (MSM) (1). Monkeypox virus (MPXV) spreads from person to person through close, prolonged contact; a small number of cases have occurred in populations who are not MSM (e.g., women and children), and testing is recommended for persons who meet the suspected case definition* (1). CDC previously developed five real-time polymerase chain reaction (PCR) assays for detection of orthopoxviruses from lesion specimens (2,3). CDC was granted 510(k) clearance for the nonvariola-orthopoxvirus (NVO)-specific PCR assay by the Food and Drug Administration. This assay was implemented within the Laboratory Response Network (LRN) in the early 2000s and became critical for early detection of MPXV and implementation of public health action in previous travel-associated cases as well as during the current outbreak (4-7). PCR assays (NVO and other Orthopoxvirus laboratory developed tests [LDT]) represent the primary tool for monkeypox diagnosis. These tests are highly sensitive, and cross-contamination from other MPXV specimens being processed, tested, or both alongside negative specimens can occasionally lead to false-positive results. This report describes three patients who had atypical rashes and no epidemiologic link to a monkeypox case or known risk factors; these persons received diagnoses of monkeypox based on late cycle threshold (Ct) values ≥34, which were false-positive test results. The initial diagnoses were followed by administration of antiviral treatment (i.e., tecovirimat) and JYNNEOS vaccine postexposure prophylaxis (PEP) to patients' close contacts. After receiving subsequent testing, none of the three patients was confirmed to have monkeypox. Knowledge gained from these and other cases resulted in changes to CDC guidance. When testing for monkeypox in specimens from patients without an epidemiologic link or risk factors or who do not meet clinical criteria (or where these are unknown), laboratory scientists should reextract and retest specimens with late Ct values (based on this report, Ct ≥34 is recommended) (8). CDC can be consulted for complex cases including those that appear atypical or questionable cases and can perform additional viral species- and clade-specific PCR testing and antiorthopoxvirus serologic testing.
自 2022 年 5 月以来,美国已发现约 2 万例猴痘病例,这是在大约 90 个国家发生的全球疫情的一部分,目前主要影响男同性恋者、双性恋者和其他与男性发生性关系的男性(MSM)(1)。猴痘病毒(MPXV)通过密切、长时间的接触在人与人之间传播;少数非 MSM 人群(如妇女和儿童)中也发生了病例,建议对符合疑似病例定义的人进行检测*(1)。CDC 此前开发了五种用于从病变标本中检测正痘病毒的实时聚合酶链反应(PCR)检测方法(2、3)。食品和药物管理局批准了针对非天花正痘病毒(NVO)的 PCR 检测方法的 510(k)清除。该检测方法于 21 世纪初在实验室反应网络(LRN)中实施,并在之前的旅行相关病例以及当前疫情中对 MPXV 的早期检测和公共卫生行动的实施至关重要(4-7)。PCR 检测(NVO 和其他正痘病毒实验室开发的检测[LDT])是猴痘诊断的主要工具。这些检测方法非常灵敏,与其他正在处理、检测或两者兼有的 MPXV 标本交叉污染偶尔会导致假阳性结果。本报告描述了三例具有非典型皮疹且与猴痘病例或已知危险因素无流行病学联系的患者;这些人根据循环阈值(Ct)值≥34 的晚期值诊断为猴痘,这是假阳性检测结果。最初的诊断后,对患者的密切接触者进行了抗病毒治疗(即特考韦瑞)和 JYNNEOS 疫苗暴露后预防(PEP)。在接受后续检测后,这三例患者均未被确认为猴痘。从这些和其他病例中获得的知识导致了 CDC 指南的改变。当对没有流行病学联系或危险因素或不符合临床标准(或这些未知)的患者标本进行猴痘检测时,实验室科学家应重新提取和重新检测 Ct 值较晚的标本(基于本报告,建议 Ct≥34)(8)。对于不典型或可疑病例和复杂病例,可咨询 CDC,并可进行额外的病毒种和进化枝特异性 PCR 检测和抗正痘病毒血清学检测。