| Project/Area Number |
06670855
|
|---|
| Research Category |
Grant-in-Aid for General Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
Dermatology
|
|---|
| Research Institution | Tokyo Medical and Dental University |
|---|
Principal Investigator |
YOKOZEKI Hiroo Tokyo Medical and Dental University, Department of Dermatology, Lecturer, 医学部, 講師 (90210608)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
MATSUNAGA Tsuyoshi Tokyo medical and Dental Univ.Department of Dermatology, Assistant, 医学部, 助手 (50239050)
|
|---|
| Project Period (FY) |
1994 – 1995
|
| Project Status |
Completed (Fiscal Year 1995)
|
| Budget Amount *help |
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1995: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1994: ¥1,400,000 (Direct Cost: ¥1,400,000)
|
|---|
| Keywords | Contact Dermatitis / T cell Activation / Costimulatory molecnles / CD80 (B7-1) / CD86 (B7-2) / Langerhans cell / T cell / T細胞 / CD80抗原 / CD86抗原 |
|---|
| Research Abstract |
Recently, an alternative CD28 ligand, CD86 (B70/B7-2) has been identified on activated B cells. It has been also found that CD86 may play an important role for costimulation of T cells in a primary immune response (Nature : 366,76-79,1993). These finding led us to determine whether CD80 and CD86 antigens express on Langerhans cells (LC) and costimulatory molecules transduced signals play a role in T cell activation in contact hypersensitivity.
We first examined CD80, CD86 expression on EC of organ cultured human skin, by staining with the monoclonal anti CD80 (L307), anti CD86Ab (IT2). Keratinocyte (KC) expressed little CD80, CD86, but both CD80 and CD86 molecules on Langerhans cell (LC) have been expressed extensively strongly after culturing. Both CD86 and CD 86 molecules have been detected in contact ddermatitis, atopic dermatitis and psoriasis. In these cases, expression of CD86 was predominantly induced. To determine whether IT2 react with 70KD glycoprotein on LC,immunoblotting method was conducted. IT2 was reacted mainly with the 70KD peptide of LC.We also examined the effect of mAb anti-CD80 or mAb anti-CD86 on the capacity of cultured EC to stimulate proliferation of allogeneic peripheral blood mononuclear cellc (PBMC). Both anti CD80 mAb and anti CD86 mAb efficiently inhibited the mixed epidermal cell-lymphocyte reaction.
These data indicate that CD86 (B70/B7-2) antigen expressed on LC may play an important role for costimulation of T cells in a primary immune response ; contact dermatitis.
|
