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DESCRIPTION (provided by applicant): The proposed R03 pilot study will combine two traditional gene delivery vectors into a novel hybrid device with potential to surpass the gene delivery efficacy of either original vector. Biomaterials have been a primary vehicle to facilitate gene delivery due to their inherent biocompatibility and adjustable properties available to influence cellular delivery mechanisms. More recently, bacterial vectors have also been used for gene delivery and provide an orthogonal set of biological engineering parameters to further influence the cellular gene delivery process. In this work, a hybrid biomaterial-bacterial device will be generated that combines the best features of both individual vectors. More specifically, previous studies using either biomaterial or bacterial vectors for targeted antigen presenting cell gene delivery will now be combined in an effort to boost gene delivery efficacy to these particular cells. Improved gene delivery as a result of the new hybrid biomaterial- biological vectors will establish the technology as innovative. More importantly, the hybrid devices will provide a completely new platform for engineering design that includes disparate tools such as polymer chemistry and molecular biology to further modify and technically advance the potency of the vectors. This will be a key theme of future grant submissions as will be the application of the new devices, facilitated through established connections between Tufts' Schools of Engineering and Medicine, as genetic vaccines against infectious disease and cancer. PUBLIC HEALTH RELEVANCE: Success will provide two health-related outcomes: 1) a completely new gene delivery device with biological and biomaterial engineering tools available for future optimization and 2) a broad platform technology to be dedicated to new disease models and more advanced therapeutic applications.
期刊论文(8)
专著(0)
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会议论文
Contemporary approaches for nonviral gene therapy.
非病毒基因治疗的当代方法。
DOI: --
发表时间: 2015
期刊: Discovery medicine
影响因子: 1.4
作者: [Jones,CharlesH, Hill,Andrew, Chen,Mingfu, Pfeifer,BlaineA]
通讯作者: Pfeifer,BlaineA
PEGylated cationic polylactides for hybrid biosynthetic gene delivery.
用于杂化生物合成基因递送的阳离子阳离子多乳酸。
DOI: 10.1021/mp500683c
发表时间: 2015-03-02
期刊: MOLECULAR PHARMACEUTICS
影响因子: 4.9
作者: [Jones, Charles H., Chen, Chih-Kuang, Chen, Mingfu, Ravikrishnan, Anitha, Zhang, Hanguang, Gollakota, Akhila, Chung, Taichun, Cheng, Chong, Pfeifer, Blaine A.]
通讯作者: Pfeifer, Blaine A.
DOI: 10.1016/j.biomaterials.2015.04.033
发表时间: 2015-07
期刊: Biomaterials
影响因子: 14
作者: [Jones CH, Gollakota A, Chen M, Chung TC, Ravikrishnan A, Zhang G, Pfeifer BA]
通讯作者: Pfeifer BA
DOI: 10.1021/mp400467x
发表时间: 2013-11-04
期刊: Molecular pharmaceutics
影响因子: 4.9
作者: [Jones CH, Chen CK, Ravikrishnan A, Rane S, Pfeifer BA]
通讯作者: Pfeifer BA
7
    Liposomal Encapsulation Vaccine Design for Pneumococcal Disease in Aged Subjects
    A Hybrid Biomaterial-biological Vector for Antigen Presenting Cell Gene Delivery
    • 批准号:
      7990629
    • 项目类别:
    • 资助金额:
      $7.24万
    • 财政年份:
      2010
    • 负责人:
      Blaine Pfeifer
    • 依托单位:
    国内基金
    海外基金
    Neo-antigens暴露对肾移植术后体液性排斥反应的影响及其机制研究
    • 批准号:
      2022J011295
    • 项目类别:
      省市级项目
    • 资助金额:
      10.0万元
    • 批准年份:
      2022
    • 负责人:
      王亚伟
    • 依托单位:
    结核分枝杆菌持续感染期抗原(latency antigens)的重组BCG疫苗研究