Department of Biochemistry, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Biotechnol Adv. 2019 Nov 15;37(7):107413. doi: 10.1016/j.biotechadv.2019.06.012. Epub 2019 Jun 26.
The gut associated lymphoid tissue has effective mechanisms in place to maintain tolerance to food antigens. These can be exploited to induce antigen-specific tolerance for the prevention and treatment of autoimmune diseases and severe allergies and to prevent serious immune responses in protein replacement therapies for genetic diseases. An oral tolerance approach for the prevention of peanut allergy in infants proved highly efficacious and advances in treatment of peanut allergy have brought forth an oral immunotherapy drug that is currently awaiting FDA approval. Several other protein antigens made in plant cells are in clinical development. Plant cell-made proteins are protected in the stomach from acids and enzymes after their oral delivery because of bioencapsulation within plant cell wall, but are released to the immune system upon digestion by gut microbes. Utilization of fusion protein technologies facilitates their delivery to the immune system, oral tolerance induction at low antigen doses, resulting in efficient induction of FoxP3 and latency-associated peptide (LAP) regulatory T cells that express immune suppressive cytokines such as IL-10. LAP and IL-10 expression represent potential biomarkers for plant-based oral tolerance. Efficacy studies in hemophilia dogs support clinical development of oral delivery of bioencapsulated antigens to prevent anti-drug antibody formation. Production of clinical grade materials in cGMP facilities, stability of antigens in lyophilized plant cells for several years when stored at ambient temperature, efficacy of oral delivery of human doses in large animal models and lack of toxicity augur well for clinical advancement of this novel drug delivery concept.
肠相关淋巴组织具有有效的机制来维持对食物抗原的耐受性。这些机制可以被利用来诱导针对自身免疫性疾病和严重过敏的抗原特异性耐受,并预防遗传疾病的蛋白质替代疗法中的严重免疫反应。一种用于预防婴儿花生过敏的口服耐受方法被证明非常有效,并且在花生过敏治疗方面的进展带来了一种正在等待 FDA 批准的口服免疫疗法药物。其他几种在植物细胞中制造的蛋白质抗原也正在临床开发中。植物细胞制造的蛋白质在口服给药后因其在植物细胞壁内的生物胶囊化而在胃中免受酸和酶的影响,但在被肠道微生物消化时会被释放到免疫系统中。融合蛋白技术的利用促进了它们向免疫系统的传递,低抗原剂量下的口服耐受诱导,从而有效地诱导了 FoxP3 和潜伏期相关肽(LAP)调节性 T 细胞的表达,这些细胞表达免疫抑制细胞因子,如 IL-10。LAP 和 IL-10 的表达代表了基于植物的口服耐受的潜在生物标志物。在血友病犬中的疗效研究支持了生物胶囊化抗原的口服递送以预防抗药物抗体形成的临床开发。在 cGMP 设施中生产临床级别的材料,在冻干的植物细胞中储存多年时保持抗原的稳定性,在大型动物模型中进行人类剂量的口服递送的有效性以及缺乏毒性,都预示着这一新的药物递送概念的临床进展良好。