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Immunogenicity of single-dose diphtheria vaccines based on PLA/PLGA microspheres in guinea pigs

机译:基于PLA / PLGA微球的单剂量白喉疫苗在豚鼠中的免疫原性

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Biodegradable polyester microspheres (MS) have shown potential for single-dose vaccines. This study examined the immunogenicity of diphtheria toxoid (Dtxd) microencapsulated in different types of poly(lactide) (PLA) and poly(lactide-co-glycolide) (PLGA) MS prepared by the methods of spray-drying and coacervation. We investigated the influence of polymer type (PLGA 50:50 of low M_w; PLA of high M_w; end-group stearylated PLAs of low M_w) and co-encapsulated excipients (BSA and/or trehalose) on Dtxd content, in vitro release and immunogenicity in guinea pigs. The co-encapsulated trehalose lowered the Dtxd entrapment efficiency in the spray-dried particles from 75 to 56%, whereas albumin alone had no effect in the spraydrying, but improved the encapsulation in the coacervation process. With the hydrophobic, end-group stearylated PLAs, Dtxd could only be encapsulated in the presence of albumin. Guinea pigs immunised with Dtxd-MS made with the relatively hydrophilic PLGA 50:50 exhibited specific and sustained antibody responses over 40 weeks, comparable to the responses to alum-adjuvanted toxoid. In contrast, undetectable or very low antibody responses were determined after immunisation with MS made with hydrophobic polymers. Surprisingly, large (15-60 #mu#m) and small (1-5 #mu#m) MS gave comparable primary antibody responses. In conclusion, the data presented confirm the feasibility of MS vaccines to induce strong, long-lasting protective antibody responses after a single immunisation.
机译:可生物降解的聚酯微球(MS)已显示出单剂量疫苗的潜力。这项研究检查了微囊化的白喉类毒素(Dtxd)在通过喷雾干燥和凝聚法制备的不同类型的聚(丙交酯)(PLA)和聚(丙交酯-共-乙交酯)(PLGA)MS中的免疫原性。我们研究了聚合物类型(低M_w的PLGA 50:50;高M_w的PLA;低M_w的端基硬脂酸PLA)和共包封的赋形剂(BSA和/或海藻糖)对Dtxd含量,体外释放和豚鼠的免疫原性。共包封的海藻糖可将喷雾干燥颗粒中Dtxd的包封率从75%降低至56%,而单独的白蛋白对喷雾干燥没有影响,但可改善凝聚过程中的包封率。使用疏水的端基硬脂酸聚乳酸,Dtxd只能在白蛋白存在的情况下进行封装。用相对亲水的PLGA 50:50制成的Dtxd-MS免疫的豚鼠在40周内表现出特异性和持续的抗体反应,与对明矾类毒素的反应相当。相反,在用疏水性聚合物制成的MS免疫后,确定无法检测到或非常低的抗体反应。出乎意料的是,大(15-60#μm)和小(1-5#μm)MS产生了可比的一抗。总之,所提供的数据证实了单次免疫后MS疫苗诱导强而持久的保护性抗体应答的可行性。

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