1988 Fiscal Year Final Research Report Summary
Analysis of Pathogenesis of lichenoid tissue reactions
Project/Area Number |
62570461
|
Research Category |
Grant-in-Aid for General Scientific Research (C)
|
Allocation Type | Single-year Grants |
Research Field |
Dermatology
|
Research Institution | Kyorin University School of Medicine |
Principal Investigator |
SHIOHARA Tetsuo Kyorin Univ. School of Medicine, Department of Dermatology, 医学部皮膚科, 助教授 (10118953)
|
Project Period (FY) |
1987 – 1988
|
Keywords | Lichenoid tissue reactions / epidermotropism / LFA-1 molecule / IFN- / LFA-1 |
Research Abstract |
We previously established a mouse model in which the LTR was experimentally induced by colal transfer of CD4^+ autoreactive cloned T cells. Using this animal model, the following conclusions can be drawn from the observation made in this project. 1. Certain autoreactive or allo-I-A reactive cloned T cells that have been proven to be epidermotropic in vivo, but not other T cells, show directional migration toward the epidermis in vitro. Studies with cell lines and recombinant cytokines indicate that keratinocyte-derived factors are responsible for the epidermotropic migration of the T cells. 2. We further investigated the effects of in vivo administration of anti-I-A, anti-CD4 and anti-LFA-1 monoclonal antibodies (mAb) on the development of LTR and delayed-type hypersensitivity (DTH) responses evoked by local transfer of the epidermotropic T cells. Prevention of the LTR was achieved with local abministration of either anti-CD4 or anti-LFA-1 mAb, but not with anti-I-A mAb, while the DTH responses were equally inhibited by all the mAb. Anti-LFA-1 mAb also inhibited the in vitro epidermotropic migration, whereas anti-I-A and anti-CD4 mAb were inactive. These results indicate that the ability of the T cells to migrate into the epidermis may depend in part on their surface expression of LFA-1. 3. To incestigate which molecules on the T cells are responsible for epidermotropic migration of the T cells, various cloned T cells were tested for their expression of CD3, CD4, CD8, CD2, Mac-1 and LFA-1. The results of flow cytometric analysis showed that LFA-1 was preferentially expressed on the surface of epidermotropic T cells. The presence of LFA-1 on T cells was necessary, but not sufficient to render the T cells-capable of migrating into the epidermis and that up-regulation of the LFA-1 was neither necessary nor sufficient to become epidermotropic.
|
Research Products
(12 results)