File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.imlet.2023.05.007
- Scopus: eid_2-s2.0-85162773488
- WOS: WOS:001008167000001
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Inactivated COVID-19 vaccines: potential concerns of antibody-dependent enhancement and original antigenic sin
Title | Inactivated COVID-19 vaccines: potential concerns of antibody-dependent enhancement and original antigenic sin |
---|---|
Authors | |
Keywords | Antibodies Antibody-Dependent Enhancement COVID-19 COVID-19 Vaccines Original Antigenic Sin SARS-CoV-2 Variants |
Issue Date | 23-May-2023 |
Publisher | Elsevier |
Citation | Immunology Letters, 2023, v. 259, p. 21-23 How to Cite? |
Abstract | Inactivated vaccine is one of the platforms employed in COVID-19 vaccines. Inactivated vaccines have been associated with concerns of antibody-dependent enhancement (ADE) and original antigenic sin (OAS), which are related to non-neutralising or poorly neutralising antibodies against the pathogen. Since inactivated COVID-19 vaccines use whole-SARS-CoV-2 virus as the immunogen, they are expected to generate antibodies against non-spike structural proteins, which are highly conservative across variants of SARS-CoV-2. These antibodies against non-spike structural proteins have found to be largely non-neutralising or poorly neutralising in nature. Hence, inactivated COVID-19 vaccines could possibly be associated with ADE and OAS, especially as novel variants emerge. This article explores the potential concern of ADE and OAS in the context of inactivated COVID-19 vaccine, and outlines the future research directions. |
Persistent Identifier | http://hdl.handle.net/10722/331467 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 1.020 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kan, Andy Ka Chun | - |
dc.contributor.author | Li, Philip Hei | - |
dc.date.accessioned | 2023-09-21T06:56:00Z | - |
dc.date.available | 2023-09-21T06:56:00Z | - |
dc.date.issued | 2023-05-23 | - |
dc.identifier.citation | Immunology Letters, 2023, v. 259, p. 21-23 | - |
dc.identifier.issn | 0165-2478 | - |
dc.identifier.uri | http://hdl.handle.net/10722/331467 | - |
dc.description.abstract | <p> Inactivated vaccine is one of the platforms employed in COVID-19 vaccines. Inactivated vaccines have been associated with concerns of antibody-dependent enhancement (ADE) and original antigenic sin (OAS), which are related to non-neutralising or poorly neutralising antibodies against the pathogen. Since inactivated COVID-19 vaccines use whole-SARS-CoV-2 virus as the immunogen, they are expected to generate antibodies against non-spike structural proteins, which are highly conservative across variants of SARS-CoV-2. These antibodies against non-spike structural proteins have found to be largely non-neutralising or poorly neutralising in nature. Hence, inactivated COVID-19 vaccines could possibly be associated with ADE and OAS, especially as novel variants emerge. This article explores the potential concern of ADE and OAS in the context of inactivated COVID-19 vaccine, and outlines the future research directions. <br></p> | - |
dc.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Immunology Letters | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Antibodies | - |
dc.subject | Antibody-Dependent Enhancement | - |
dc.subject | COVID-19 | - |
dc.subject | COVID-19 Vaccines | - |
dc.subject | Original Antigenic Sin | - |
dc.subject | SARS-CoV-2 Variants | - |
dc.title | Inactivated COVID-19 vaccines: potential concerns of antibody-dependent enhancement and original antigenic sin | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.imlet.2023.05.007 | - |
dc.identifier.scopus | eid_2-s2.0-85162773488 | - |
dc.identifier.volume | 259 | - |
dc.identifier.spage | 21 | - |
dc.identifier.epage | 23 | - |
dc.identifier.isi | WOS:001008167000001 | - |
dc.identifier.issnl | 0165-2478 | - |