Flamand V, Donckier V, Demoor F X, Le Moine A, Matthys P, Vanderhaeghen M L, Tagawa Y, Iwakura Y, Billiau A, Abramowicz D, Goldman M
Laboratory of Experimental Immunology, Free University of Brussels, Belgium.
J Immunol. 1998 May 15;160(10):4666-9.
To investigate the consequences of CD40 engagement on the neonatal induction of transplantation tolerance, BALB/c mice were injected at birth with (A/J x BALB/c) F1 spleen cells together with activating anti-CD40 mAb and grafted 4 wk later with A/J skin. Whereas A/J allografts were accepted in mice neonatally injected with F1 cells and control Ab, they were acutely rejected in mice injected with F1 cells and anti-CD40 mAb. Neonatal administration of anti-CD40 mAb resulted in enhanced anti-A/J CTL activity, increased IFN-gamma, and decreased IL-4 production by donor-specific T cells in vitro. Experiments using anti-cytokine mAb and IFN-gamma-deficient mice demonstrated that CD40 ligation prevents neonatal allotolerance through an IFN-gamma- and IL-12-dependent pathway. Finally, we found that newborn T cells express less CD40L than adult T cells upon TCR engagement. Taken together these data indicate that insufficiency of CD40/CD40L interactions contribute to neonatal transplantation tolerance.
为研究CD40激活对新生小鼠移植耐受诱导的影响,出生时给BALB/c小鼠注射(A/J×BALB/c)F1脾细胞及激活型抗CD40单克隆抗体,并在4周后移植A/J皮肤。新生期注射F1细胞和对照抗体的小鼠可接受A/J同种异体移植,但注射F1细胞和抗CD40单克隆抗体的小鼠则发生急性排斥反应。新生期给予抗CD40单克隆抗体可增强体外供体特异性T细胞的抗A/J CTL活性、增加IFN-γ产生并减少IL-4分泌。使用抗细胞因子单克隆抗体和IFN-γ缺陷小鼠进行的实验表明,CD40连接通过IFN-γ和IL-12依赖途径阻止新生期同种异体耐受。最后,我们发现新生T细胞在TCR激活后表达的CD40L比成年T细胞少。这些数据表明,CD40/CD40L相互作用不足有助于新生期移植耐受。