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Analysis of monoclonal T cells in benign dermatoses related to mycosis fungoides.

Research Project

Project/Area Number 10670790
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Dermatology
Research InstitutionTottori University

Principal Investigator

HAGARI Yoshitaka  Tottori University, Department of Dermatology, Assistant Professor, 医学部附属病院, 講師 (70201704)

Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥2,400,000 (Direct Cost: ¥2,400,000)
Fiscal Year 1999: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1998: ¥1,900,000 (Direct Cost: ¥1,900,000)
KeywordsPityriasis lichenoides / PCR / TCR / Monoclonality / In-situ hybridization / Immunohistochemistry / Surfase marker / T cell / T細胞受容体 / 免疫グロブリン遺伝子 / 菌状息肉症 / 急性痘瘡状苔蘚状粃糠疹 / 悪性リンパ腫
Research Abstract

Pityriasis lichenoides has been regarded as a benign inflammatory disorder belonging to the parapsoriasis group. However, based on its association with cutaneous T cell lymphoma (CTCL) or the presence of monoclonal populations in infiltrates, it has been hypothesized that pityriasis lichenoides is part of the CTCL disease sectrum. For validation of this hypothesis, the monoclonal populations in pityriasis lichenoides should express the same phenotype as CTCL CID4^+ Tlymphocyte.
In this study, we analysed infiltrates in 7 cases of pityriasis lichenoides (6 cases of pityriasis lichenoides et varioliformis acuta and one case of pityriasis lichenoides chronica) using praffin-embedded specimens.
1. By amplifying the rearranged TCR-γ genes, monoclonal populations were detected in 6 of 7 cases of pityriasis lichenoides.
2. These amplified bands were recovered and sequenced. These data showed that the PCR-based method adequately amplified the rearranged TCR-γ genes and specified the gene segments used in the rearrangement processes.
3. We prepared pairs of mirror sections that gave the same histological picture as a mirror image. In each pair, in-situ hybridization (ISH) using the amplified band as a probe on one section and immunohistochemistry using UCHL1, anti-CD8, or anti-CD4 antibodies on the other section were performed. By comparing these sections, the phenotypes of the ISH-positive cells were determined as UCHL1^+, CD8^-, CD4^+ cells.
These results demonstrated that pityriasis lichenoides qualified as a member of parapsoriasis. Furthermore, we suggest that the interrelationship between monoclonal CD4^+ cells and reactive CD8^+ cells affects the biological behavior of the disease in the CTCL disease spectrum.

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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