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急性痘疮样苔藓样糠疹皮损的免疫表型和病毒研究。

Immunophenotyping and viral studies in pityriasis lichenoides et varioliformis acuta lesions.

机构信息

Department of Dermatology, Rambam Health Care Campus and The Bruce Rappaport Faculty of Medicine, Haifa, Israel.

Department of Pathology, Rambam Health Care Campus and The Bruce Rappaport Faculty of Medicine, Haifa, Israel.

出版信息

J Cutan Pathol. 2024 Oct;51(10):790-798. doi: 10.1111/cup.14679. Epub 2024 Jul 7.

DOI:10.1111/cup.14679
PMID:38973067
Abstract

BACKGROUND

The underlying pathogenesis of pityriasis lichenoides et varioliformis acuta (PLEVA) remains unclear, although immunologic injury and viral etiology have been suggested.

OBJECTIVE

To evaluate and expand the immunophenotype of PLEVA and to search for possible viral pathogens.

METHODS

Formalin-fixed, paraffin-embedded specimens of 20 patients with PLEVA and 9 patients with common inflammatory dermatoses (ID) were studied for immunophenotyping and for human herpesvirus (HHV) 1 and 2, cytomegalovirus (CMV), HHV-8, parvovirus B19, and Epstein-Barr virus (EBV) immunohistochemistry. The presence of HHV-6, HHV-7, and enteroviruses was assayed molecularly.

RESULTS

The numbers of CD8 T cells and T-cell intracellular antigen-1 (TIA-1) cells were statistically significantly higher in PLEVA compared to the ID group. Immunohistochemistry for human HHV-1 and HHV-2, CMV and HHV-8, parvovirus B19, and in situ hybridization for EBV were all negative. There was molecular evidence for HHV-7 in only one PLEVA case (5%). Molecular studies for HHV-6 and enterovirus involvement were negative in all the PLEVA specimens.

CONCLUSIONS

The predominant T-cell infiltrate in PLEVA is dominated by CD8 cells, and by increased numbers of TIA1 cells, which may indicate a cytotoxic T-cell damage to the epidermis. Viral presence was not detected.

摘要

背景

尽管已经提出免疫损伤和病毒病因,但 pityriasis lichenoides et varioliformis acuta(PLEVA)的潜在发病机制仍不清楚。

目的

评估和扩展 PLEVA 的免疫表型,并寻找可能的病毒病原体。

方法

对 20 例 PLEVA 患者和 9 例常见炎症性皮肤病(ID)患者的福尔马林固定、石蜡包埋标本进行免疫表型分析,并进行人类疱疹病毒(HHV)1 和 2、巨细胞病毒(CMV)、HHV-8、细小病毒 B19 和 EBV 免疫组织化学检测。HHV-6、HHV-7 和肠道病毒的存在通过分子检测进行评估。

结果

与 ID 组相比,PLEVA 中 CD8 T 细胞和 T 细胞内抗原-1(TIA-1)细胞的数量明显更高。HHV-1 和 HHV-2、CMV 和 HHV-8、细小病毒 B19 的人类 HHV 免疫组化和 EBV 的原位杂交均为阴性。仅在 1 例 PLEVA 病例(5%)中存在 HHV-7 的分子证据。所有 PLEVA 标本的 HHV-6 和肠道病毒参与的分子研究均为阴性。

结论

PLEVA 中的主要 T 细胞浸润主要由 CD8 细胞和 TIA1 细胞数量增加组成,这可能表明表皮的细胞毒性 T 细胞损伤。未检测到病毒存在。

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