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颗粒大小、抗原负载量、剂量及额外佐剂对抗抗原负载聚乳酸微颗粒免疫反应的影响

Influence of particle size, antigen load, dose and additional adjuvant on the immune response from antigen loaded PLA microparticles.

作者信息

Katare Yogesh K, Muthukumaran T, Panda Amulya K

机构信息

National Institute of Immunology, Product Development Cell, Aruna Asaf Ali Marg, New Delhi 110067, India.

出版信息

Int J Pharm. 2005 Sep 14;301(1-2):149-60. doi: 10.1016/j.ijpharm.2005.05.028.

Abstract

Polylactide (PLA) polymer particles entrapping tetanus toxoid (TT) were evaluated in terms of particle size, antigen load, dose and additional adjuvant for achieving high and sustained anti-TT antibody titer from single point intramuscular immunization. Admixture of polymer entrapped TT and alum improved the immune response in comparison to particle-based immunization. High and long lasting antibody titer was achieved upon immunization with 2-8 microm size particles. Microparticles within the size range 50-150 microm elicited very low serum antibody response. Immunization with very small particles (<2 microm) and with intermediate size range particles (10-70 microm) elicited comparable antibody response from single point immunization but lower in comparison to that achieved while immunizing with 2-8 microm size particles. Potentiation of antibody response on immunization of admixture of microparticles and alum was also dependent on particle size. These results indicate the need of optimal particle sizes in micron ranges for improved humoral response from single point immunization. Increasing antigen load on polymer particles was found to have positive influence on generation of antibody titers from particle based immunization. Maximum peak antibody titer of approximately 300 microg/mL was achieved on day 50 upon immunization with particles having highest load of antigen (94 microg/mg of polymer). Increase in dose of polymer entrapped antigen resulted in concomitant increase in peak antibody titers indicating the importance of antigen stability, particle size and load on generating reproducible immune response. Optimization of particle size, antigen load, dose and use of additional adjuvant resulted in high and sustained anti-TT antibody titers over a period of more than 250 days from single point immunization. Serum anti-TT antibody titers from single point immunization of admixrure of PLA particles and alum was comparable with immunization from two divided doses of alum adsorbed TT.

摘要

对包裹破伤风类毒素(TT)的聚乳酸(PLA)聚合物颗粒进行了评估,涉及粒径、抗原负载量、剂量以及额外佐剂,目的是通过单点肌肉注射免疫实现高且持续的抗TT抗体滴度。与基于颗粒的免疫相比,聚合物包裹的TT与明矾的混合物改善了免疫反应。用2 - 8微米大小的颗粒进行免疫可实现高且持久的抗体滴度。50 - 150微米大小范围内的微粒引发的血清抗体反应非常低。用非常小的颗粒(<2微米)和中等大小范围的颗粒(10 - 70微米)进行单点免疫引发的抗体反应相当,但与用2 - 8微米大小的颗粒免疫相比更低。微粒与明矾混合物免疫时抗体反应的增强也取决于粒径。这些结果表明,为了从单点免疫中改善体液反应,需要微米范围内的最佳粒径。发现增加聚合物颗粒上的抗原负载量对基于颗粒的免疫产生抗体滴度有积极影响。在用抗原负载量最高(94微克/毫克聚合物)的颗粒免疫后第50天,达到了约300微克/毫升的最大峰值抗体滴度。包裹抗原的聚合物剂量增加导致峰值抗体滴度随之增加,表明抗原稳定性、粒径和负载量对产生可重复免疫反应的重要性。粒径、抗原负载量、剂量的优化以及额外佐剂的使用导致从单点免疫在超过250天的时间内产生高且持续的抗TT抗体滴度。PLA颗粒与明矾混合物单点免疫产生的血清抗TT抗体滴度与两次分剂量明矾吸附TT免疫相当。

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