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二十一例儿童多系统炎症综合征阑尾与急性阑尾炎标本的病理分析:一项横断面研究。

Pathologic Analysis of Twenty-one Appendices From Children With Multisystem Inflammatory Syndrome Compared to Specimens of Acute Appendicitis: A Cross-sectional Study.

机构信息

From the Department of Pediatrics with Clinical Assessment Unit, Medical University of Warsaw, Warsaw, Poland.

Department of Pediatric Infectious Diseases, Wroclaw Medical University, Wrocław, Poland.

出版信息

Pediatr Infect Dis J. 2024 Jun 1;43(6):525-531. doi: 10.1097/INF.0000000000004264. Epub 2024 Feb 7.

Abstract

BACKGROUND

Multisystem inflammatory syndrome in children (MIS-C) is a rare, severe complication of coronavirus disease 2019, commonly involving the gastrointestinal tract. Some children with MIS-C undergo appendectomy before the final diagnosis. There are several hypotheses explaining the pathomechanism of MIS-C, including the central role of the viral antigen persistence in the gut, associated with lymphocyte exhaustion. We aimed to examine appendectomy specimens from MIS-C patients and assess their pathologic features, as well as the presence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigens.

METHODS

In this cross-sectional study we included 21 children with MIS-C who underwent appendectomy. The control group included 21 sex- and age-matched children with acute appendicitis (AA) unrelated to SARS-CoV-2 infection. Histologic evaluation of appendiceal specimens included hematoxylin and eosin staining and immunohistochemical identification of lymphocyte subpopulations, programmed cell death protein-1 (PD-1) and SARS-CoV-2 nucleocapsid antigen.

RESULTS

Appendices of MIS-C patients lacked neutrophilic infiltrate of muscularis propria typical for AA (14% vs. 95%, P < 0.001). The proportion of CD20+ to CD5+ cells was higher in patients with MIS-C (P = 0.04), as was the proportion of CD4+ to CD8+ (P < 0.001). We found no proof of SARS-CoV-2 antigen presence, nor lymphocyte exhaustion, in the appendices of MIS-C patients.

CONCLUSIONS

The appendiceal muscularis of patients with MIS-C lack edema and neutrophilic infiltration typical for AA. SARS-CoV-2 antigens and PD-1 are absent in the appendices of children with MIS-C. These findings argue against the central role of SARS-CoV-2 persistence in the gut and lymphocyte exhaustion as the major triggers of MIS-C.

摘要

背景

儿童多系统炎症综合征(MIS-C)是 2019 年冠状病毒病(COVID-19)的一种罕见且严重的并发症,通常涉及胃肠道。一些患有 MIS-C 的儿童在最终诊断前接受阑尾切除术。有几种假说解释了 MIS-C 的发病机制,包括病毒抗原在肠道中的持续存在与淋巴细胞衰竭的核心作用。我们旨在检查 MIS-C 患者的阑尾切除标本,并评估其病理特征,以及严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)抗原的存在。

方法

在这项横断面研究中,我们纳入了 21 名接受阑尾切除术的 MIS-C 患儿。对照组包括 21 名性别和年龄匹配的与 SARS-CoV-2 感染无关的急性阑尾炎(AA)患儿。阑尾标本的组织学评估包括苏木精和伊红染色以及淋巴细胞亚群、程序性细胞死亡蛋白 1(PD-1)和 SARS-CoV-2 核衣壳抗原的免疫组织化学鉴定。

结果

MIS-C 患儿的阑尾缺乏 AA 典型的固有肌层中性粒细胞浸润(14% vs. 95%,P < 0.001)。MIS-C 患儿的 CD20+/CD5+细胞比例较高(P = 0.04),CD4+/CD8+比例也较高(P < 0.001)。我们在 MIS-C 患儿的阑尾中未发现 SARS-CoV-2 抗原存在或淋巴细胞衰竭的证据。

结论

MIS-C 患儿的阑尾固有肌缺乏 AA 典型的水肿和中性粒细胞浸润。SARS-CoV-2 抗原和 PD-1 在 MIS-C 患儿的阑尾中不存在。这些发现表明,SARS-CoV-2 在肠道中的持续存在和淋巴细胞衰竭并不是 MIS-C 的主要触发因素。

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