Instituto de Medicina Molecular, University of Lisbon Lisbon, Portugal.
Front Immunol. 2011 Oct 19;2:56. doi: 10.3389/fimmu.2011.00056. eCollection 2011.
Monoclonal antibodies (mAb) have been shown effective in inducing immune tolerance in a range of animal models of autoimmunity, allergy, and transplantation. We investigated whether CD4-blockade, effective in inducing transplantation tolerance, could prevent systemic immune responses leading to anaphylaxis. We found that treatment with a non-depleting anti-CD4 mAb could prevent peanut-induced anaphylaxis following subsequent systemic exposure to crude peanut extract (CPE). Furthermore, the effect of CD4-blockade did not interfere with overall immune competence, as anti-CD4 treated mice remained fully competent to respond to unrelated antigens. Protection from anaphylaxis correlated with increased frequency of Foxp3⁺ regulatory T cells (Treg), and was abrogated following Treg depletion. Taken together our data suggest that activation of T cells by CPE in presence of CD4-blockade leads to Treg expansion that can prevent peanut-induced anaphylaxis.
单克隆抗体(mAb)已被证明在一系列自身免疫、过敏和移植的动物模型中具有诱导免疫耐受的作用。我们研究了是否 CD4 阻断,在诱导移植耐受方面有效,是否可以防止导致过敏反应的全身性免疫反应。我们发现,用非耗竭性抗 CD4 mAb 治疗可以防止随后全身暴露于粗花生提取物(CPE)后引起的花生过敏反应。此外,CD4 阻断的作用不会干扰整体免疫能力,因为抗 CD4 治疗的小鼠仍然完全有能力对无关抗原作出反应。对过敏反应的保护与 Foxp3⁺调节性 T 细胞(Treg)的频率增加有关,并且在 Treg 耗竭后被阻断。综上所述,我们的数据表明,在 CD4 阻断的情况下,CPE 激活 T 细胞会导致 Treg 的扩增,从而可以预防花生引起的过敏反应。