Literature DB >> 22043954

Adenovirus-vectored drug-vaccine duo as a potential driver for conferring mass protection against infectious diseases.

Jianfeng Zhang1, E Bart Tarbet, Haroldo Toro, De-chu C Tang.   

Abstract

The disease-fighting power of vaccines has been a public health bonanza credited with the worldwide reduction of mortality and morbidity. The goal to further amplify its power by boosting vaccine coverage requires the development of a new generation of rapid-response vaccines that can be mass produced at low costs and mass administered by nonmedical personnel. The new vaccines also have to be endowed with a higher safety margin than that of conventional vaccines. The nonreplicating adenovirus-vectored vaccine holds promise in boosting vaccine coverage because the vector can be rapidly manufactured in serum-free suspension cells in response to a surge in demand, and noninvasively administered by nasal spray into human subjects in compliance with evolutionary medicine. In contrast to parenteral injection, noninvasive mucosal vaccination minimizes systemic inflammation. Moreover, pre-existing adenovirus immunity does not interfere appreciably with the potency of an adenovirus-vectored nasal vaccine. Nasal administration of adenovirus vectors encoding pathogen antigens is not only fear-free and painless, but also confers rapid and sustained protection against mucosal pathogens as a drug-vaccine duo since adenovirus particles alone without transgene expression can induce an anti-influenza state in the airway. In addition to human vaccination, animals can also be mass immunized by this class of vectored vaccines.

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Year:  2011        PMID: 22043954     DOI: 10.1586/erv.11.141

Source DB:  PubMed          Journal:  Expert Rev Vaccines        ISSN: 1476-0584            Impact factor:   5.217


  9 in total

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2.  Adenovirus vector-based prime-boost vaccination via heterologous routes induces cervicovaginal CD8+ T cell responses against HPV16 oncoproteins.

Authors:  Nicolas Çuburu; Selina Khan; Cynthia D Thompson; Rina Kim; Jort Vellinga; Roland Zahn; Douglas R Lowy; Gert Scheper; John T Schiller
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3.  Noninvasive vaccination as a casus belli to redeem vaccine value in the face of anti-vaccine movements.

Authors:  De-Chu C Tang
Journal:  Integr Mol Med       Date:  2017-07-24

4.  Intramuscular delivery of adenovirus serotype 5 vector expressing humanized protective antigen induces rapid protection against anthrax that may bypass intranasally originated preexisting adenovirus immunity.

Authors:  Shipo Wu; Zhe Zhang; Rui Yu; Jun Zhang; Ying Liu; Xiaohong Song; Shaoqiong Yi; Ju Liu; Jianqin Chen; Ying Yin; Junjie Xu; Lihua Hou; Wei Chen
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Review 5.  Prophylactic vaccine delivery systems against epidemic infectious diseases.

Authors:  Chao Pan; Hua Yue; Li Zhu; Guang-Hui Ma; Heng-Liang Wang
Journal:  Adv Drug Deliv Rev       Date:  2021-07-17       Impact factor: 17.873

6.  A trail blazed through DNA vaccine, noninvasive vaccine, and innate-adaptive immunity duo.

Authors:  De-chu Christopher Tang
Journal:  Hum Vaccin Immunother       Date:  2014       Impact factor: 3.452

Review 7.  Role of Recombinant DNA Technology to Improve Life.

Authors:  Suliman Khan; Muhammad Wajid Ullah; Rabeea Siddique; Ghulam Nabi; Sehrish Manan; Muhammad Yousaf; Hongwei Hou
Journal:  Int J Genomics       Date:  2016-12-08       Impact factor: 2.326

8.  Paradoxical modulation of influenza by intranasal administration of non-replicating adenovirus particles.

Authors:  De-Chu Christopher Tang
Journal:  PLoS One       Date:  2020-11-12       Impact factor: 3.240

9.  Recombinant influenza vaccines.

Authors:  E S Sedova; D N Shcherbinin; A I Migunov; Iu A Smirnov; D Iu Logunov; M M Shmarov; L M Tsybalova; B S Naroditskiĭ; O I Kiselev; A L Gintsburg
Journal:  Acta Naturae       Date:  2012-10       Impact factor: 1.845

  9 in total

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