Goldmann Katja, Ensminger Stephan M, Spriewald Bernd M
Department of Internal Medicine 5-Hematology/Oncology and Institute for Clinical Immunology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Clin Vaccine Immunol. 2012 Nov;19(11):1758-64. doi: 10.1128/CVI.00186-12. Epub 2012 Aug 29.
Oral tolerance is a promising approach to induce unresponsiveness to various antigens. The development of tolerogenic vaccines could be exploited in modulating the immune response in autoimmune disease and allograft rejection. In this study, we investigated a nonviral gene transfer strategy for inducing oral tolerance via antigen-encoding chitosan-DNA nanoparticles (NP). Oral application of ovalbumin (OVA)-encoding chitosan-DNA NP (OVA-NP) suppressed the OVA-specific delayed-type hypersensitivity (DTH) response and anti-OVA antibody formation, as well as spleen cell proliferation following OVA stimulation. Cytokine expression patterns following OVA stimulation in vitro showed a shift from a Th1 toward a Th2/Th3 response. The OVA-NP-induced tolerance was transferable from donor to naïve recipient mice via adoptive spleen cell transfer and was mediated by CD4(+)CD25(+) T cells. These findings indicate that nonviral oral gene transfer can induce regulatory T cells for antigen-specific immune modulation.
口服耐受是一种诱导机体对各种抗原无反应性的有前景的方法。耐受性疫苗的研发可用于调节自身免疫性疾病和同种异体移植排斥反应中的免疫应答。在本研究中,我们研究了一种通过抗原编码壳聚糖 - DNA纳米颗粒(NP)诱导口服耐受的非病毒基因转移策略。口服卵清蛋白(OVA)编码壳聚糖 - DNA NP(OVA - NP)可抑制OVA特异性迟发型超敏反应(DTH)、抗OVA抗体形成以及OVA刺激后的脾细胞增殖。体外OVA刺激后的细胞因子表达模式显示从Th1反应向Th2/Th3反应转变。OVA - NP诱导的耐受性可通过过继性脾细胞转移从供体小鼠转移至未接触过抗原的受体小鼠,并由CD4(+)CD25(+) T细胞介导。这些发现表明非病毒口服基因转移可诱导调节性T细胞进行抗原特异性免疫调节。