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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Induction of antigen-specific tolerance by oral administration of Lactococcus lactis delivered immunodominant DQ8-restricted gliadin peptide in sensitized nonobese diabetic Abo Dq8 transgenic mice.
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Induction of antigen-specific tolerance by oral administration of Lactococcus lactis delivered immunodominant DQ8-restricted gliadin peptide in sensitized nonobese diabetic Abo Dq8 transgenic mice.

机译:在致敏的非肥胖糖尿病Abo Dq8转基因小鼠中,口服乳酸乳球菌可诱导免疫特异性DQ8限制的麦醇溶蛋白肽诱导抗原特异性耐受。

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摘要

Active delivery of recombinant autoantigens or allergens at the intestinal mucosa by genetically modified Lactococcus lactis (LL) provides a novel therapeutic approach for the induction of tolerance. Celiac disease is associated with either HLA-DQ2- or HLA-DQ8-restricted responses to specific antigenic epitopes of gliadin, and may be treated by induction of Ag-specific tolerance. We investigated whether oral administration of LL-delivered DQ8-specific gliadin epitope induces Ag-specific tolerance. LL was engineered to secrete a deamidated DQ8 gliadin epitope (LL-eDQ8d) and the induction of Ag-specific tolerance was studied in NOD AB degrees DQ8 transgenic mice. Tolerance was assessed by delayed-type hypersensitivity reaction, cytokine measurements, eDQ8d-specific proliferation, and regulatory T cell analysis. Oral administration of LL-eDQ8d induced suppression of local and systemic DQ8-restricted T cell responses in NOD AB degrees DQ8 transgenic mice. Treatment resulted in an Ag-specific decrease of the proliferative capacity of inguinal lymph node (ILN) cells and lamina propria cells. Production of IL-10 and TGF-beta and a significant induction of Foxp3(+) regulatory T cells were associated with the eDQ8d-specific suppression induced by LL-eDQ8d. These data provide support for the development of effective therapeutic approaches for gluten-sensitive disorders using orally administered Ag-secreting LL. Such treatments may be effective even in the setting of established hypersensitivity.
机译:基因改造的乳酸乳球菌(LL)在肠粘膜上主动递送重组自身抗原或变应原,为诱导耐受提供了一种新颖的治疗方法。腹腔疾病与对麦醇溶蛋白的特定抗原表位的HLA-DQ2-或HLA-DQ8-限制性反应有关,并且可以通过诱导Ag特异性耐受来治疗。我们调查了口服给药的LL传递DQ8特异性麦醇溶蛋白表位是否诱导Ag特异性耐受。 LL被工程化以分泌脱酰胺基的DQ8醇溶蛋白表位(LL-eDQ8d),并在NOD AB度DQ8转基因小鼠中研究了Ag特异性耐受的诱导。通过迟发型超敏反应,细胞因子测量,eDQ8d特异性增殖和调节性T细胞分析评估耐受性。在NOD AB度DQ8转基因小鼠中,口服LL-eDQ8d可诱导抑制局部和全身性DQ8限制性T细胞反应。治疗导致腹股沟淋巴结(ILN)细胞和固有层细胞的Ag特异性减少。 IL-10和TGF-β的产生以及Foxp3(+)调节性T细胞的显着诱导与LL-eDQ8d诱导的eDQ8d特异性抑制有关。这些数据为使用口服Ag分泌的LL的面筋敏感性疾病的有效治疗方法的开发提供了支持。即使在已经建立的超敏反应中,这种治疗也可能是有效的。

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