Detection of low-level tumor cells in allergic contact dermatitis induced by mechlorethamine in patients with mycosis fungoides

被引:15
作者
Veelken, H
Sklar, JL
Wood, GS
机构
[1] VET AFFAIRS MED CTR,CLEVELAND,OH 44106
[2] UNIV FREIBURG,DEPT MED,W-7800 FREIBURG,GERMANY
[3] BRIGHAM & WOMENS HOSP,DEPT PATHOL,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
[5] CASE WESTERN RESERVE UNIV,DEPT DERMATOL,CLEVELAND,OH 44106
[6] CASE WESTERN RESERVE UNIV,DEPT PATHOL,CLEVELAND,OH 44106
[7] CASE WESTERN RESERVE UNIV,SKIN DIS RES CTR,CLEVELAND,OH 44106
关键词
mycosis fungoides; allergic contact dermatitis; T-cell receptor; PCR;
D O I
10.1111/1523-1747.ep12345517
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Two patients with histologically proven mycosis fungoides, a malignancy of phenotypically mature T cells, received a topical challenge with mechlorethamine to areas of clinically uninvolved skin to exclude possible hypersensitivity reactions to this chemotherapeutic agent, In both patients, allergic contact dermatitis (ACD) developed at the sites of the application and resolved completely after withdrawal of mechlorethamine. The lesions were biopsied and analyzed for the presence of clonal T-cell receptor (TCR)-gamma gene rearrangements using two polymerase chain reaction (PCR)-based assays involving denaturing gradient gel electrophoresis (PCR/DGGE) and ribonuclease protection analysis (PCR/RPA), The former method has a clonal detection threshold of 10(-3)-10(-2), while the latter has a sensitivity of 10(-5), In both cases, the ACD lesions were polyclonal by PCR/DGGE, In contrast, PCR/RPA detected tumor-specific TCR-gamma gene rearrangements in these same lesions, This indicates that the ACD lesions contained tumor cells at a density within the 10(-5)-10(-2) range, Analysis of peripheral blood mononuclear cells from both patients failed to detect the malignant clone and showed the same result as blood from four normal individuals, The normal skin fi om one patient also lacked detectable TCR-gamma gene rearrangements, These results indicate that mycosis fungoides tumor cells are present within ACD lesions induced in mycosis fungoides patients and that this phenomenon does not appear to be due to the ubiquitous presence of detectable levels of these tumor cells in the blood or shin. These findings might be explained by nonspecific recruitment of malignant T cells to sites of local inflammation mediated by non-neoplastic antigen-specific T cells. Alternatively, they might be due to the local proliferation of very rare tumor cells in apparently normal skin in response to cytokines generated during the ACD reaction, In either case, the present study offers evidence that the malignant cells in mycosis fungoides retain at least some capability of responding in vivo to physiologic stimuli.
引用
收藏
页码:685 / 688
页数:4
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