首页> 外文期刊>Journal of cutaneous pathology >Pityriasis lichenoides et varioliformis acuta and pityriasis lichenoides chronica: comparison of lesional T-cell subsets and investigation of viral associations.
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Pityriasis lichenoides et varioliformis acuta and pityriasis lichenoides chronica: comparison of lesional T-cell subsets and investigation of viral associations.

机译:糠疹糠疹和地衣糠vari和糠疹糠疹:病变T细胞亚群的比较和病毒关联的研究。

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BACKGROUND: Pityriasis lichenoides (PL) exhibits a broad clinical spectrum that includes both acute and chronic forms. The precise biologic mechanisms underlying PL remain unclear. OBJECTIVES: To evaluate the immunohistochemical characteristics of PL and to investigate lesional T-cell subsets and the possible role of viral infection in its pathogenesis. PATIENTS AND METHODS: Samples from 10 patients with PL et varioliformis acuta (PLEVA) and 13 with PL chronica (PLC) were analyzed immunohistochemically. Epstein-Barr virus early regions were assayed by in situ hybridization and T-cell receptor-gamma (TCR-gamma) gene rearrangements were assayed by polymerase chain reaction (PCR). We also utilized PCR to assay for human herpesvirus-8 (HHV-8) DNA in 51 patients with PL and in 25 controls. RESULTS: Lymphocytes expressing CD8 and T-cell intracellular antigen-1 were more abundant in patients with PLEVA than with PLC, whereas CD4+ lymphocytes and FOXP3-positive regulatory T-cells were more abundant in PLC. HHV-8 DNA was present in 11 of 51 (21.6%) PL patients and 0 of 25 controls. A clonal TCR-gamma gene rearrangement was observed in only one patient with PLEVA. CONCLUSIONS: Our data suggests that PL may represent an inflammatory condition induced by various triggering agents, such as HHV-8, rather than a lymphoproliferative disorder. PLEVA, characterized by an acute course with severe symptoms, may indicate a relative lack of regulatory T-cells in comparison with PLC.
机译:背景:糠疹糠疹(Pityriasis lichenoides,PL)具有广泛的临床范围,包括急性和慢性形式。 PL的确切生物学机制仍不清楚。目的:评估PL的免疫组织化学特征,并研究病变T细胞亚群以及病毒感染在其发病机理中的可能作用。病人和方法:免疫组织化学法分析了10例PL等距畸形患者(PLEVA)和13例PL慢性病(PLC)患者的样本。通过原位杂交检测爱泼斯坦-巴尔病毒的早期区域,并通过聚合酶链反应(PCR)检测T细胞受体-γ(TCR-γ)基因重排。我们还利用PCR检测了51例PL患者和25例对照中的人类疱疹病毒8(HHV-8)DNA。结果:PLEVA患者中表达CD8和T细胞胞内抗原1的淋巴细胞比PLC更丰富,而CD4 +淋巴细胞和FOXP3阳性调节性T细胞在PLC中更丰富。 HHV-8 DNA存在于51名PL患者中的11名(21.6%)和25名对照中的0名。仅一名PLEVA患者观察到了克隆性TCR-γ基因重排。结论:我们的数据表明PL可能代表由多种触发剂(例如HHV-8)而非淋巴增生性疾病引起的炎性疾病。 PLEVA的特征是具有严重症状的急性病程,与PLC相比可能表明相对缺乏调节性T细胞。

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