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蕈样肉芽肿早期患者及斑片状副银屑病患者的淋巴细胞功能与染色体畸变

Lymphocyte function and chromosome aberrations in patients with early mycosis fungoides and parapsoriasis en plaques.

作者信息

Clemmensen O J, Bendtzen K, Andersen V, Wulf H C, Niebuhr E, Thomsen K, Bendixen G

出版信息

J Invest Dermatol. 1983 Oct;81(4):308-13. doi: 10.1111/1523-1747.ep12519402.

Abstract

Thirteen patients with stage I or II mycosis fungoides (MF) and 10 patients with large-plaque parapsoriasis en plaques (PEP) were examined for immunologic and cytogenetic disturbances. Total lymphocyte counts and immunoglobulin concentrations in the blood were normal. In vitro lymphocyte responses to polyclonal activators and various antigens in standard concentrations were normal. However, titration of phytohemagglutinin and concanavalin A (ConA) disclosed significantly lowered responses to suboptimal concentrations in the patient group, most pronounced in patients with MF II. ConA-induced leukocyte migration inhibitory factor (LIF) production, tested in an indirect leukocyte migration inhibitory assay, was low in the patient group. Furthermore spontaneous LIF production in vitro and small amounts of serum LIF were demonstrated in a few patients. The chromosomal banding pattern, sister chromatid exchange, and break frequency were within normal limits except for 3 translocations in the MF group. It is concluded that even in early-stage MF a pathologic function of blood lymphocytes can be demonstrated, when sensitive methods are applied. The findings might be important for monitoring disease activity and effect of treatment.

摘要

对13例Ⅰ期或Ⅱ期蕈样肉芽肿(MF)患者和10例大斑块状副银屑病(PEP)患者进行了免疫和细胞遗传学紊乱检查。患者血液中的淋巴细胞总数和免疫球蛋白浓度均正常。体外淋巴细胞对多克隆激活剂和标准浓度的各种抗原的反应正常。然而,对植物血凝素和刀豆球蛋白A(ConA)进行滴定发现,患者组对次优浓度的反应明显降低,在Ⅱ期MF患者中最为明显。在间接白细胞迁移抑制试验中检测到,ConA诱导的白细胞迁移抑制因子(LIF)产生在患者组中较低。此外,少数患者在体外有自发LIF产生,血清中也有少量LIF。除MF组有3例易位外,染色体带型、姐妹染色单体交换和断裂频率均在正常范围内。结论是,当应用敏感方法时,即使在MF早期也可证明血液淋巴细胞存在病理功能。这些发现可能对监测疾病活动和治疗效果具有重要意义。

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