Literature DB >> 24962722

Intranasal formulations: promising strategy to deliver vaccines.

Peggy Riese1, Priya Sakthivel, Stephanie Trittel, Carlos A Guzmán.   

Abstract

INTRODUCTION: The emergence of new diseases and the lack of efficient vaccines against numerous non-treatable pathogens require the development of novel vaccination strategies. To date, only a few mucosal vaccines have been approved for humans. This was in part due to i) the use of live attenuated vaccines, which are not suitable for certain groups of individuals, ii) safety concerns derived from implementation in humans of some mucosal vaccines, iii) the poor stability, absorption and immunogenicity of antigens delivered by the mucosal route and iv) the limited number of available technologies to overcome the bottlenecks associated with mucosal antigen delivery. Recent advances make feasible the development of efficacious mucosal vaccines with adequate safety profile. Thus, currently intranasal vaccines represent an attractive and valid alternative to conventional vaccines. AREAS COVERED: The present review is focused on the potentials and limitations of market-approved intranasal vaccines and promising candidates undergoing clinical investigations. Furthermore, emerging strategies to overcome main bottlenecks including efficient breaching of the mucosal barrier and safety concerns by implementation of new adjuvants and delivery systems are discussed. EXPERT OPINION: The rational design of intranasal vaccines requires an in-depth understanding of the anatomic, physicochemical and barrier properties of the nasal mucosa, as well as the molecular mechanisms governing the activation of the local innate and adaptive immune system. This would provide the critical knowledge to establish effective approaches to deliver vaccine antigens across the mucosal barrier, supporting the stimulation of a long-lasting protective response at both mucosal and systemic levels. Current developments in the area of adjuvants, nanotechnologies and mucosal immunology, together with the identification of surface receptors that can be exploited for cell targeting and manipulating their physiological properties, will become instrumental for developing a new generation of more effective intranasal vaccines.

Entities:  

Keywords:  adjuvants; antigen delivery systems; approved intranasal vaccines; microfold cell targeting; mucosal vaccines

Mesh:

Substances:

Year:  2014        PMID: 24962722     DOI: 10.1517/17425247.2014.931936

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  24 in total

Review 1.  Gas-filled microbubbles: Novel mucosal antigen-delivery system for induction of anti-pathogen's immune responses in the gut.

Authors:  Blaise Corthésy; Gilles Bioley
Journal:  Gut Microbes       Date:  2017-05-25

2.  Ex vivo antigen-pulsed PBMCs generate potent and long lasting immunity to infection when administered as a vaccine.

Authors:  Sudeep Kumar; Raju Sunagar; Giang Pham; Edmund J Gosselin; David Nalin
Journal:  Vaccine       Date:  2017-01-06       Impact factor: 3.641

3.  Intranasal delivery of a protein subunit vaccine using a Tobacco Mosaic Virus platform protects against pneumonic plague.

Authors:  Paul M Arnaboldi; Mariya Sambir; Christina D'Arco; Lauren A Peters; Jos F M L Seegers; Lloyd Mayer; Alison A McCormick; Raymond J Dattwyler
Journal:  Vaccine       Date:  2016-10-13       Impact factor: 3.641

4.  Evaluation of mucosal adjuvants and immunization routes for the induction of systemic and mucosal humoral immune responses in macaques.

Authors:  Ronald S Veazey; Asna Siddiqui; Katja Klein; Viviana Buffa; Lucia Fischetti; Lara Doyle-Meyers; Deborah F King; John S Tregoning; Robin J Shattock
Journal:  Hum Vaccin Immunother       Date:  2015       Impact factor: 3.452

5.  A long-lasting, single-dose nasal vaccine for Ebola: a practical armament for an outbreak with significant global impact.

Authors:  Kristina Jonsson-Schmunk; Maria A Croyle
Journal:  Expert Rev Anti Infect Ther       Date:  2015-03-23       Impact factor: 5.091

6.  The Potential of Neuraminidase as an Antigen for Nasal Vaccines To Increase Cross-Protection against Influenza Viruses.

Authors:  Atsushi Kawai; Yasuyuki Yamamoto; Takuto Nogimori; Kohei Takeshita; Takuya Yamamoto; Yasuo Yoshioka
Journal:  J Virol       Date:  2021-08-11       Impact factor: 5.103

7.  Mucosal delivery switches the response to an adjuvanted tuberculosis vaccine from systemic TH1 to tissue-resident TH17 responses without impacting the protective efficacy.

Authors:  Mark T Orr; Elyse A Beebe; Thomas E Hudson; David Argilla; Po-Wei D Huang; Valerie A Reese; Christopher B Fox; Steven G Reed; Rhea N Coler
Journal:  Vaccine       Date:  2015-11-03       Impact factor: 3.641

8.  A role for the CCR5-CCL5 interaction in the preferential migration of HSV-2-specific effector cells to the vaginal mucosa upon nasal immunization.

Authors:  Sunyi Joo; Aldina Suwanto; Ayuko Sato; Rika Nakahashi-Ouchida; Hiromi Mori; Yohei Uchida; Shintaro Sato; Yosuke Kurashima; Yoshikazu Yuki; Kohtaro Fujihashi; Yasushi Kawaguchi; Hiroshi Kiyono
Journal:  Mucosal Immunol       Date:  2019-09-24       Impact factor: 7.313

Review 9.  Synthetic Nanoparticles for Vaccines and Immunotherapy.

Authors:  Darrell J Irvine; Melissa C Hanson; Kavya Rakhra; Talar Tokatlian
Journal:  Chem Rev       Date:  2015-07-08       Impact factor: 60.622

10.  Dynamic Changes in the Nasal Microbiome Associated With Disease Activity in Patients With Granulomatosis With Polyangiitis.

Authors:  Rennie L Rhee; Jiarui Lu; Kyle Bittinger; Jung-Jin Lee; Lisa M Mattei; Antoine G Sreih; Sherry Chou; Jonathan J Miner; Noam A Cohen; Brendan J Kelly; Hongzhe Lee; Peter C Grayson; Ronald G Collman; Peter A Merkel
Journal:  Arthritis Rheumatol       Date:  2021-07-31       Impact factor: 15.483

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