Immunosuppressive effect on T cell activation by interleukin-16-cDNA-transfected human squamous cell line

被引:11
作者
Fujita, T
Matsumoto, Y
Hirai, I
Ezoe, K
Saito, T
Yagihashi, A
Torigoe, T
Homma, K
Takahashi, S
Cruikshank, WW
Jimbow, K
Sato, N
机构
[1] Sapporo Med Univ, Sch Med, Div Plast Surg, Sapporo, Hokkaido 0608543, Japan
[2] Sapporo Med Univ, Sch Med, Dept Pathol, Sapporo, Hokkaido 0608543, Japan
[3] Sapporo Med Univ, Sch Med, Dept Lab Diag, Sapporo, Hokkaido 0608543, Japan
[4] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
关键词
D O I
10.1006/cimm.2000.1657
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is well known that it is difficult to induce an immunotolerance with allogeneic skin transplantation. We attempted to find the immunosuppressive protocol for prolonging skin allograft rejection by using interleukin-16 because IL-16 is considered one of the natural ligands to CD4 molecules. First we examined whether synergistic immunosuppressive effects of recombinant IL-16 plus anti-CD4 mAbs are induced in mixed lymphocyte reaction (MLR). Next we used IL-16-cDNA-transfected OSC-20 (human oral squamous cell carcinoma cell line) as an in vitro model of the epidermal keratinocyte equivalent and examined whether this transfectant could inhibit the activation of allogeneic T cells. Our data indicated that IL-16 clearly inhibited human MLR and that IL-16 increased synergistically the immunosuppressive effect of anti-CD4 mAb. We also used IL-16 transfectant and this produced more than 50 ng/ml of IL-16 in the supernatant by which human MLR was significantly inhibited. Furthermore, this transfectant also inhibited the activation of allogeneic lymphocytes stimulated directly with transfectant cells. These results indicated that the IL-16-producing allogeneic skin graft might have a local immunosuppressive action that would prolong graft survival. (C) 2000 Academic Press.
引用
收藏
页码:54 / 60
页数:7
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