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免疫组化自动检测固定石蜡包埋样本中的淀粉样蛋白:与新鲜冷冻组织免疫荧光数据的比较。

Immunohistochemical typing of amyloid in fixed paraffin-embedded samples by an automatic procedure: Comparison with immunofluorescence data on fresh-frozen tissue.

机构信息

Pathology Unit, City of Health and Science Hospital, Turin, Italy.

Department of Medical Sciences, University of Turin, Turin, Italy.

出版信息

PLoS One. 2021 Aug 24;16(8):e0256306. doi: 10.1371/journal.pone.0256306. eCollection 2021.

Abstract

Amyloidosis comprises a spectrum of disorders characterized by the extracellular deposition of amorphous material, originating from an abnormal serum protein. The typing of amyloid into its many variants represents a pivotal step for a correct patient management. Several methods are currently used, including mass spectrometry, immunofluorescence, immunohistochemistry, and immunogold labeling. The aim of the present study was to investigate the accuracy and reliability of immunohistochemistry by means of a recently developed amyloid antibody panel applicable on fixed paraffin-embedded tissues in an automated platform. Patients with clinically and pathologically proven amyloidosis were divided into two cohorts: a pilot one, which included selected amyloidosis cases from 2009 to 2018, and a retrospective one (comprising all consecutive amyloidosis cases analyzed between November 2018 and May 2020). The above-referred panel of antibodies for amyloid classification was tested in all cases using an automated immunohistochemistry platform. When fresh-frozen material was available, immunofluorescence was also performed. Among 130 patients, a total of 143 samples from different organs was investigated. They corresponded to 51 patients from the pilot cohort and 79 ones from the retrospective cohort. In 82 cases (63%), fresh-frozen tissue was tested by immunofluorescence, serving to define amyloid subtype only in 30 of them (36.6%). On the contrary, the automated immunohistochemistry procedure using the above-referred new antibodies allowed to establish the amyloid type in all 130 cases (100%). These included: ALλ (n = 60, 46.2%), ATTR (n = 29, 22.3%), AA (n = 19, 14.6%), ALκ (n = 18, 13.8%), ALys (n = 2, 1.5%), and Aβ2M amyloidosis (n = 2, 1.5%). The present immunohistochemistry antibody panel represents a sensitive, reliable, fast, and low-cost method for amyloid typing. Since immunohistochemistry is available in most pathology laboratories, it may become the new gold standard for amyloidosis classification, either used alone or combined with mass spectrometry in selected cases.

摘要

淀粉样变包括一组以细胞外无定形物质沉积为特征的疾病,这些物质源自异常的血清蛋白。将淀粉样变分为多种变体是正确管理患者的关键步骤。目前有几种方法,包括质谱法、免疫荧光法、免疫组化和免疫金标记。本研究的目的是通过一种新的、适用于自动化平台上固定石蜡包埋组织的淀粉样变抗体检测试剂盒,研究免疫组化的准确性和可靠性。将经临床和病理证实的淀粉样变患者分为两个队列:一个是试点队列,包括 2009 年至 2018 年的部分淀粉样变病例;另一个是回顾性队列,包括 2018 年 11 月至 2020 年 5 月期间所有连续的淀粉样变病例。使用自动化免疫组化平台对所有病例进行上述淀粉样变分类抗体检测。当有新鲜冷冻组织时,也进行免疫荧光检测。在 130 名患者中,共检测了来自不同器官的 143 个样本。它们来自试点队列的 51 名患者和回顾性队列的 79 名患者。在 82 例(63%)患者中,通过免疫荧光检测了新鲜冷冻组织,仅在其中 30 例(36.6%)中确定了淀粉样变亚型。相反,使用上述新抗体的自动化免疫组化程序可以确定 130 例患者的淀粉样变类型(100%)。这些类型包括:ALλ(n = 60,46.2%)、ATTR(n = 29,22.3%)、AA(n = 19,14.6%)、ALκ(n = 18,13.8%)、ALys(n = 2,1.5%)和 Aβ2M 淀粉样变(n = 2,1.5%)。本研究中的免疫组化抗体检测试剂盒是一种敏感、可靠、快速、低成本的淀粉样变检测方法。由于免疫组化在大多数病理实验室都可以进行,因此它可能成为淀粉样变分类的新标准,单独使用或与质谱法联合使用,适用于特定病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a38e/8384180/07986ce236b7/pone.0256306.g001.jpg

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