Live unattenuated vaccines for controlling viral diseases, including COVID-19

被引:4
作者
Chen, Ji-Ming [1 ]
机构
[1] Foshan Univ, Sch Life Sci & Engn, Foshan 528231, Guangdong, Peoples R China
关键词
antibody; antiviral; COVID-19; glycan; safety; SARS-CoV-2; vaccine; virus; NATURAL ANTIBODY; HUMAN SERUM; VIRUS; NEUTRALIZATION; IMMUNOGENICITY; GLYCOPROTEINS; INACTIVATION; EXPRESSION; CELLS; HIV-1;
D O I
10.1002/jmv.26453
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Live unattenuated vaccines (LUVs) have been neglected for decades, due to widespread prejudice against their safety, even though they have successfully controlled yellow fever and adenovirus infection in humans as well as rinderpest and infectious bursal disease in animals. This review elucidated that LUVs could be highly safe with selective use of neutralizing antivirus antibodies, natural antiglycan antibodies, nonantibody antivirals, and ectopic inoculation. Also, LUVs could be of high efficacy, high development speed, and high production efficiency, with the development of humanized monoclonal antibodies and other modern technologies. They could circumvent antibody-dependent enhancement and maternal-derived antibody interference. With these important advantages, LUVs could be more powerful than other vaccines for controlling some viral diseases, and they warrant urgent investigation with animal experiments and clinical trials for defeating the COVID-19 pandemic caused by the novel coronavirus SARS-CoV-2.
引用
收藏
页码:1943 / 1949
页数:7
相关论文
共 70 条
  • [1] Immunogenicity of influenza virus vaccine is increased by anti-Gal-mediated targeting to airitigen-presenting cells
    Abdel-Motal, Ussama M.
    Guay, Heath M.
    Wigglesworth, Kim
    Welsh, Raymond M.
    Galili, Uri
    [J]. JOURNAL OF VIROLOGY, 2007, 81 (17) : 9131 - 9141
  • [2] Increased immunogenicity of HIV-1 p24 and gp120 following immunization with gp120/p24 fusion protein vaccine expressing α-gal epitopes
    Abdel-Motal, Ussama M.
    Wang, Shixia
    Awad, Amany
    Lu, Shan
    Wigglesworth, Kim
    Galili, Uri
    [J]. VACCINE, 2010, 28 (07) : 1758 - 1765
  • [3] LYTIC ANTI-ALPHA-GALACTOSYL ANTIBODIES FROM PATIENTS WITH CHRONIC CHAGAS-DISEASE RECOGNIZE NOVEL O-LINKED OLIGOSACCHARIDES ON MUCIN-LIKE GLYCOSYL-PHOSPHATIDYLINOSITOL-ANCHORED GLYCOPROTEINS OF TRYPANOSOMA-CRUZI
    ALMEIDA, IC
    FERGUSON, MAJ
    SCHENKMAN, S
    TRAVASSOS, LR
    [J]. BIOCHEMICAL JOURNAL, 1994, 304 : 793 - 802
  • [4] [Anonymous], IMM VACC BIOL
  • [5] The influence of natural antibody specificity on antigen immunogenicity
    Benatuil, L
    Kaye, J
    Rich, RF
    Fishman, JA
    Green, WR
    Iacomini, J
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (09) : 2638 - 2647
  • [6] BioRender, COVID 19 VACC THER T
  • [7] COVID-19: immunopathology and its implications for therapy
    Cao, Xuetao
    [J]. NATURE REVIEWS IMMUNOLOGY, 2020, 20 (05) : 269 - 270
  • [8] Viraemia suppressed in HIV-1-infected humans by broadly neutralizing antibody 3BNC117
    Caskey, Marina
    Klein, Florian
    Lorenzi, Julio C. C.
    Seaman, Michael S.
    West, Anthony P., Jr.
    Buckley, Noreen
    Kremer, Gisela
    Nogueira, Lilian
    Braunschweig, Malte
    Scheid, Johannes F.
    Horwitz, Joshua A.
    Shimeliovich, Irina
    Ben-Avraham, Sivan
    Witmer-Pack, Maggi
    Platten, Martin
    Lehmann, Clara
    Burke, Leah A.
    Hawthorne, Thomas
    Gorelick, Robert J.
    Walker, Bruce D.
    Keler, Tibor
    Gulick, Roy M.
    Faetkenheuer, Gerd
    Schlesinger, Sarah J.
    Nussenzweig, Michel C.
    [J]. NATURE, 2015, 522 (7557) : 487 - +
  • [9] SARS-CoV-2 replicating in nonprimate mammalian cells probably have critical advantages for COVID-19 vaccines due to anti-Gal antibodies: A minireview and proposals
    Chen, Ji-Ming
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2021, 93 (01) : 351 - 356
  • [10] Potential for elimination of SAR-CoV-2 through vaccination as inspired by elimination of multiple influenza viruses through natural pandemics or mass vaccination
    Chen, Ji-Ming
    Sun, Ying-Xue
    Chen, Ji-Wang
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2020, 92 (11) : 2453 - 2457