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The Chimera of S1 and N Proteins of Sars-Cov-2: Can It Be a Potential Vaccine Candidate for Covid-19? Publisher Pubmed



Kumar A1 ; Ladha A2 ; Choudhury A3 ; Ikbal AMA4 ; Bhattacharjee B5 ; Das T6 ; Gupta G2, 7 ; Sharma C2 ; Sarbajna A8 ; Mandal SC9 ; Choudhury MD1 ; Ali N10 ; Slama P11 ; Rezaei N12, 13, 14 Show All Authors
Authors
  1. Kumar A1
  2. Ladha A2
  3. Choudhury A3
  4. Ikbal AMA4
  5. Bhattacharjee B5
  6. Das T6
  7. Gupta G2, 7
  8. Sharma C2
  9. Sarbajna A8
  10. Mandal SC9
  11. Choudhury MD1
  12. Ali N10
  13. Slama P11
  14. Rezaei N12, 13, 14
  15. Palit P15
  16. Tiwari ON16

Source: Expert Review of Vaccines Published:2022


Abstract

Introduction: Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has emerged as one of the biggest global health issues. Spike protein (S) and nucleoprotein (N), the major immunogenic components of SARS-CoV-2, have been shown to be involved in the attachment and replication of the virus inside the host cell. Areas covered: Several investigations have shown that the SARS-CoV-2 nucleoprotein can elicit a cell-mediated immune response capable of regulating viral replication and lowering viral burden. However, the development of an effective vaccine that can stop the transmission of SARS-CoV-2 remains a matter of concern. Literature was retrieved using the keywords COVID-19 vaccine, role of nucleoprotein as vaccine candidate, spike protein, nucleoprotein immune responses against SARS-CoV-2, and chimera vaccine in PubMed, Google Scholar, and Google. Expert opinion: We have focussed on the use of chimera protein, consisting of N and S-1 protein components of SARS-CoV-2, as a potential vaccine candidate. This may act as a polyvalent mixed recombinant protein vaccine to elicit a strong T and B cell immune response, which will be capable of neutralizing the wild and mutated variants of SARS-CoV-2, and also restricting its attachment, replication, and budding in the host cell. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
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