Literature DB >> 25788109

Novel antigen delivery technologies: a review.

Deepika Jain1, Vikas Jain, Ranjit Singh.   

Abstract

Over the past few years, new insights into immunobiology and delivery systems have allowed the development of better vaccines and for a wider range of diseases. Currently available vaccines represent outstanding success story in modern medicine and have had a dramatic effect on morbidity and mortality worldwide. Conventional vaccines have been based on live attenuated, or killed, viruses or bacteria, or recombinant proteins from these organisms. The design of live attenuated vaccines depended to some extent on serendipity and resulted in low success rates. Both live attenuated and killed vaccines require handling of live pathogens and are associated with safety problems. Despite the success of vaccines, there is a clear need for novel antigen delivery technologies to improve vaccine efficacy and safety. Antigen stability, safety, and immunogenicity are the key hurdles in development of novel antigen delivery technologies. Nowadays, various novel drug delivery systems are becoming one of the fastest growing sectors in the pharmaceutical and biotechnological industries. Delivery of vaccines via oral, intranasal, transcutaneous, and intradermal routes will decrease the risk of needle-borne diseases and may eliminate the need for trained personnel and sterile equipment. Currently, various techniques involving DNA vaccines, adjuvants, nanoparticles, liposome, microneedle, and NanoMAP technology are being developed and evaluated. This review focuses on the current development of some novel vaccine delivery systems and will explore the non-parenteral routes of vaccine administrations.

Year:  2011        PMID: 25788109     DOI: 10.1007/s13346-011-0014-6

Source DB:  PubMed          Journal:  Drug Deliv Transl Res        ISSN: 2190-393X            Impact factor:   4.617


  70 in total

1.  Principles of transcutaneous immunization using cholera toxin as an adjuvant.

Authors:  T Scharton-Kersten; G M Glenn; R Vassell; J Yu; D Walwender; C R Alving
Journal:  Vaccine       Date:  1999-10-01       Impact factor: 3.641

Review 2.  Taking the sting out of shots: control of vaccination-associated pain and adverse reactions.

Authors:  E C Reis; R M Jacobson; S Tarbell; B G Weniger
Journal:  Pediatr Ann       Date:  1998-06       Impact factor: 1.132

Review 3.  Vaccine developments.

Authors:  M A Liu
Journal:  Nat Med       Date:  1998-05       Impact factor: 53.440

4.  Oral vaccination of animals with antigens encapsulated in alginate microspheres.

Authors:  T L Bowersock; H HogenEsch; M Suckow; P Guimond; S Martin; D Borie; S Torregrosa; H Park; K Park
Journal:  Vaccine       Date:  1999-03-26       Impact factor: 3.641

5.  Effect of lecithins on BCG-alginate-PLL microcapsule particle size and stability upon storage.

Authors:  A Esquisabel; R M Hernández; M Igartua; A R Gascón; B Calvo; J L Pedraz
Journal:  J Microencapsul       Date:  2000 May-Jun       Impact factor: 3.142

6.  Production of alginate microspheres by internal gelation using an emulsification method.

Authors:  L Chan; H Lee; P Heng
Journal:  Int J Pharm       Date:  2002-08-21       Impact factor: 5.875

Review 7.  Enhancing oral vaccine potency by targeting intestinal M cells.

Authors:  Ali Azizi; Ashok Kumar; Francisco Diaz-Mitoma; Jiri Mestecky
Journal:  PLoS Pathog       Date:  2010-11-11       Impact factor: 6.823

8.  Microneedle-based transcutaneous immunisation in mice with N-trimethyl chitosan adjuvanted diphtheria toxoid formulations.

Authors:  Suzanne M Bal; Zhi Ding; Gideon F A Kersten; Wim Jiskoot; Joke A Bouwstra
Journal:  Pharm Res       Date:  2010-06-18       Impact factor: 4.200

9.  Biodegradable and biocompatible poly(DL-lactide-co-glycolide) microspheres as an adjuvant for staphylococcal enterotoxin B toxoid which enhances the level of toxin-neutralizing antibodies.

Authors:  J H Eldridge; J K Staas; J A Meulbroek; T R Tice; R M Gilley
Journal:  Infect Immun       Date:  1991-09       Impact factor: 3.441

10.  Liposomal delivery of p-ialB and p-omp25 DNA vaccines improves immunogenicity but fails to provide full protection against B. melitensis challenge.

Authors:  Nicola J Commander; James M Brewer; Brendan W Wren; Stephen A Spencer; Alastair P Macmillan; Judith A Stack
Journal:  Genet Vaccines Ther       Date:  2010-07-16
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