Skin biopsy processing for rapid molecular diagnosis and histopathologic interpretation: application to Kaposi sarcoma in East Africa.

IF 2.8 2区 医学 Q3 IMMUNOLOGY
Jason C Manning, Xinying Chu, Juan Boza, Racheal Ayanga, Hilda Muwando, Robert Lukande, Marcelo Horenstein, Toby Maurer, Ethel Cesarman, Aggrey Semeere, Jeffrey Martin, David Erickson
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Abstract

Background: Kaposi sarcoma (KS) is a cancer of viral origin (Kaposi sarcoma-associated herpesvirus; KSHV) for which the detection of KSHV DNA is an attractive target for a rapid, automatable diagnostic test. We previously demonstrated favorable diagnostic accuracy using loop-mediated isothermal amplification (LAMP) to quantitate KSHV DNA in lesional skin biopsies, though extracting DNA from the punch biopsies was the time-limiting step. Herein, we describe the development of a biopsy processing tool called Slicer to enable rapid nucleic acid testing in addition to traditional histopathological interpretation.

Methods: Slicer divides skin punch biopsies into two ½-cylinders and a thin, cross-sectional slice. The thin slice enables a previously demonstrated, equipment-free alkaline extraction termed ColdSHOT while the remaining ½-cylinders are available for histopathological diagnosis and additional molecular testing as needed. Slicer prototypes were used on skin punch biopsies collected from patients in Uganda who were referred for clinical suspicion of KS.

Results: For 27 patient samples, the combination of Slicer and ColdSHOT sample processing with LAMP testing resulted in qualitative KSHV DNA detection that was fully concordant with US-based histopathological diagnoses. Additional analysis demonstrated compatibility of Slicer and ColdSHOT with qPCR for KSHV DNA quantitation.

Conclusions: These results warrant further investigation using a larger set of skin biopsies and indicate that the Slicer and ColdSHOT could enable accurate KS diagnosis within a few hours of biopsy collection with minimal equipment.

快速分子诊断和组织病理学解释的皮肤活检处理:在东非卡波西肉瘤中的应用。
背景:卡波西肉瘤(KS)是一种病毒起源的癌症(卡波西肉瘤相关疱疹病毒;KSHV DNA的检测是一种快速、自动化诊断测试的有吸引力的目标。我们之前证明了使用环介导等温扩增(LAMP)在病变皮肤活检中定量KSHV DNA的良好诊断准确性,尽管从穿孔活检中提取DNA是有时间限制的步骤。在这里,我们描述了一种称为切片机的活检处理工具的发展,除了传统的组织病理学解释外,还可以进行快速核酸检测。方法:切片机将皮肤穿孔活检切片分成两个半圆柱体和一个薄的横截面切片。薄切片可用于先前演示的,称为ColdSHOT的无设备碱性提取,而剩余的½圆柱体可用于组织病理学诊断和必要的额外分子检测。切片机原型用于从乌干达因临床怀疑KS而转诊的患者收集的皮肤穿刺活检。结果:对于27例患者样本,将Slicer和ColdSHOT样品处理与LAMP检测相结合,可获得定性的KSHV DNA检测,与基于美国的组织病理学诊断完全一致。进一步的分析证明了Slicer和ColdSHOT与qPCR的兼容性,用于KSHV DNA定量。结论:这些结果值得进一步研究,使用更大的皮肤活检,并表明Slicer和ColdSHOT可以在几个小时的活检收集中使用最少的设备进行准确的KS诊断。
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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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