Suppr超能文献

皮肤T细胞淋巴瘤中克隆性T细胞在表皮的定位。

Localization of clonal T cells to the epidermis in cutaneous T-cell lymphoma.

作者信息

Fivenson D P, Hanson C A, Nickoloff B J

机构信息

Department of Dermatology, Henry Ford Hospital, Detroit, MI 48202.

出版信息

J Am Acad Dermatol. 1994 Nov;31(5 Pt 1):717-23. doi: 10.1016/s0190-9622(94)70231-4.

Abstract

BACKGROUND

Mycosis fungoides (MF) is a form of cutaneous T-cell lymphoma (CTCL) characterized by progression of clonal, epidermotropic T cells with the proliferative (Ki-67+) T-cell fraction primarily confined to the epidermis in early CTCL.

OBJECTIVE

Our purpose was to determine whether the malignant clone (recognized by its clonal T-cell receptor [TCR] rearrangement) might also be localized to the epidermal compartment by differential Southern blot analysis.

METHODS

A rapid heat-saline technique was used to separately isolate epidermal and dermal DNA from 11 patients with CTCL (1 with disease in the pre-MF stage, 4 with patch-stage MF, 3 with plaque-stage MF, 1 with tumor-stage MF, 1 with Sézary syndrome, and 1 with non-MF peripheral T-cell lymphoma). Whole and heat-saline separated 6 mm biopsy specimens (obtained from the same lesion) were analyzed by standard Southern blotting with 5 to 10 micrograms of DNA digested with BamHI, HindIII, or EcoRI in each case. Filters were probed with a 32P-labeled TCR-C beta complementary DNA. Skin compartment localization of TCR-C beta rearrangement was compared with results of diagnostic immunophenotyping and expression of proliferating cell nuclear antigen.

RESULTS

DNA yields were as follows: from the whole specimens, 14.5 to 62.5 micrograms; from epidermal sheets, 2 to 42.5 micrograms; and from the dermis specimens, 2.5 to 25.5 micrograms. Whole and separated specimens from one patient with plaque-stage disease, three with patch-stage disease, and one patient with pre-MF disease revealed no rearrangement. Six patients had detectable gene rearrangements in the whole specimen by Southern blot; four of six had identical rearrangements in only the epidermal fragment (including the Sézary syndrome biopsy specimen) and not the dermis. The other two patients had only dermal TCR-C beta rearrangement. No relation was seen between immunophenotype or proliferating cell nuclear antigen expression and the localization of TCR-C beta rearrangements. However, the degree of epidermotropism significantly correlated with the presence of TCR-C beta rearrangements in the epidermal sheets.

CONCLUSION

This study demonstrates that the malignant clone in CTCL can be localized to the epidermal compartment in most cases in which a TCR rearrangement is detectable and that these clones are associated with epidermal proliferation of lymphocytes. This technique of differential epidermal versus dermal Southern analysis for TCR rearrangement may improve sensitivity by helping to distinguish reactive from malignant T-cell populations in future studies of the pathogenesis of CTCL.

摘要

背景

蕈样肉芽肿(MF)是皮肤T细胞淋巴瘤(CTCL)的一种形式,其特征为克隆性、亲表皮性T细胞的进展,在CTCL早期,增殖性(Ki-67+)T细胞部分主要局限于表皮。

目的

我们的目的是通过差异Southern印迹分析确定恶性克隆(通过其克隆性T细胞受体[TCR]重排识别)是否也定位于表皮区室。

方法

采用快速热盐技术从11例CTCL患者(1例处于MF前期疾病,4例为斑块期MF,3例为斑片期MF,1例为肿瘤期MF,1例为Sezary综合征,1例为非MF外周T细胞淋巴瘤)中分别分离表皮和真皮DNA。对完整的和经热盐分离的6mm活检标本(取自同一病变)进行标准Southern印迹分析,每种情况下用5至10μg经BamHI、HindIII或EcoRI消化的DNA。用32P标记的TCR-Cβ互补DNA对滤膜进行杂交检测。将TCR-Cβ重排的皮肤区室定位与诊断性免疫表型分析结果及增殖细胞核抗原的表达进行比较。

结果

DNA产量如下:完整标本为14.5至62.5μg;表皮片为2至42.5μg;真皮标本为2.5至25.5μg。1例斑块期疾病患者、3例斑片期疾病患者和1例MF前期疾病患者的完整和分离标本均未显示重排。6例患者通过Southern印迹在完整标本中检测到基因重排;其中4例在仅表皮片段(包括Sezary综合征活检标本)中有相同重排,而真皮中没有。另外2例患者仅真皮有TCR-Cβ重排。免疫表型或增殖细胞核抗原表达与TCR-Cβ重排的定位之间未见相关性。然而,亲表皮程度与表皮片中TCR-Cβ重排的存在显著相关。

结论

本研究表明,在大多数可检测到TCR重排的CTCL病例中,恶性克隆可定位于表皮区室,且这些克隆与淋巴细胞的表皮增殖相关。这种用于TCR重排的差异表皮与真皮Southern分析技术,在未来CTCL发病机制研究中,通过帮助区分反应性与恶性T细胞群体,可能会提高敏感性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验