Literature DB >> 15844624

Development of antibody-targeted vaccines.

Tibor Keler1, LiZhen He, Robert F Graziano.   

Abstract

The use of monoclonal antibodies for immunotherapy has been validated by the commercialization of multiple monoclonal antibody products for oncology, infectious diseases and autoimmune diseases. In addition to their application as 'naked' antibodies, they have been used as delivery vehicles for cytotoxic agents to cancer cells. The exquisite specificity of antibodies can also be exploited to initiate and/or enhance the immune response to tumors or infectious agents by targeting the relevant antigen to antigen-presenting cells (APCs). Such antibody-targeted vaccines (ATVs) have demonstrated remarkable activity in preclinical models by eliminating the need for adjuvant and repetitive boosting, overcoming immunological non-responsiveness, inducing mucosal immunity and eliciting therapeutic cytotoxic T-cell-mediated antitumor effects. A variety of different receptors on APCs have been exploited for targeting antigens, which may allow optimization for specific immune responses. Selective targeting to appropriate receptors on APC subsets combined with strong activating signals is important for generating potent cytolytic T-cell responses. Studies have also suggested that ATVs may be selectively exploited to induce tolerance against antigens for treatment against transplant rejection or autoimmune diseases. The clinical development of this new class of antibody-based products has recently been initiated.

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Year:  2005        PMID: 15844624

Source DB:  PubMed          Journal:  Curr Opin Mol Ther        ISSN: 1464-8431


  3 in total

Review 1.  Recent advances using FcRn overexpression in transgenic animals to overcome impediments of standard antibody technologies to improve the generation of specific antibodies.

Authors:  Imre Kacskovics; Judit Cervenak; Anna Erdei; Richard A Goldsby; John E Butler
Journal:  MAbs       Date:  2011-09-01       Impact factor: 5.857

2.  Hybrid biosynthetic gene therapy vector development and dual engineering capacity.

Authors:  Charles H Jones; Anitha Ravikrishnan; Mingfu Chen; Ryan Reddinger; Mahmoud Kamal Ahmadi; Snehal Rane; Anders P Hakansson; Blaine A Pfeifer
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-11       Impact factor: 11.205

3.  FcRn overexpression in mice results in potent humoral response against weakly immunogenic antigen.

Authors:  Attila Végh; Judit Cervenak; István Jankovics; Imre Kacskovics
Journal:  MAbs       Date:  2011-03-01       Impact factor: 5.857

  3 in total

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