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- Publisher Website: 10.1136/gutjnl-2021-326563
- Scopus: eid_2-s2.0-85126224389
- PMID: 35140064
- WOS: WOS:000754021900001
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Article: Gut microbiota composition is associated with SARS-CoV- 2 vaccine immunogenicity and adverse events
Title | Gut microbiota composition is associated with SARS-CoV- 2 vaccine immunogenicity and adverse events |
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Authors | |
Issue Date | 2022 |
Citation | Gut, 2022, v. 71, n. 6, p. 1106-1116 How to Cite? |
Abstract | Objective: The gut microbiota plays a key role in modulating host immune response. We conducted a prospective, observational study to examine gut microbiota composition in association with immune responses and adverse events in adults who have received the inactivated vaccine (CoronaVac; Sinovac) or the mRNA vaccine (BNT162b2; BioNTech; Comirnaty). Design: We performed shotgun metagenomic sequencing in stool samples of 138 COVID-19 vaccinees (37 CoronaVac and 101 BNT162b2 vaccinees) collected at baseline and 1 month after second dose of vaccination. Immune markers were measured by SARS-CoV-2 surrogate virus neutralisation test and spike receptor-binding domain IgG ELISA. Results: We found a significantly lower immune response in recipients of CoronaVac than BNT162b2 vaccines (p<0.05). Bifidobacterium adolescentis was persistently higher in subjects with high neutralising antibodies to CoronaVac vaccine (p=0.023) and their baseline gut microbiome was enriched in pathways related to carbohydrate metabolism (linear discriminant analysis (LDA) scores >2 and p<0.05). Neutralising antibodies in BNT162b2 vaccinees showed a positive correlation with the total abundance of bacteria with flagella and fimbriae including Roseburia faecis (p=0.028). The abundance of Prevotella copri and two Megamonas species were enriched in individuals with fewer adverse events following either of the vaccines indicating that these bacteria may play an anti-inflammatory role in host immune response (LDA scores>3 and p<0.05). Conclusion: Our study has identified specific gut microbiota markers in association with improved immune response and reduced adverse events following COVID-19 vaccines. Microbiota-targeted interventions have the potential to complement effectiveness of COVID-19 vaccines. |
Persistent Identifier | http://hdl.handle.net/10722/341348 |
ISSN | 2023 Impact Factor: 23.0 2023 SCImago Journal Rankings: 8.052 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ng, Siew C. | - |
dc.contributor.author | Peng, Ye | - |
dc.contributor.author | Zhang, Lin | - |
dc.contributor.author | Mok, Chris K.P. | - |
dc.contributor.author | Zhao, Shilin | - |
dc.contributor.author | Li, Amy | - |
dc.contributor.author | Ching, Jessica Y.L. | - |
dc.contributor.author | Liu, Yingzhi | - |
dc.contributor.author | Yan, Shuai | - |
dc.contributor.author | Chan, Dream L.S. | - |
dc.contributor.author | Zhu, Jie | - |
dc.contributor.author | Chen, Chunke | - |
dc.contributor.author | Fung, Adrian C.H. | - |
dc.contributor.author | Wong, Kenneth K.Y. | - |
dc.contributor.author | Hui, David S.C. | - |
dc.contributor.author | Chan, Francis K.L. | - |
dc.contributor.author | Tun, Hein M. | - |
dc.date.accessioned | 2024-03-13T08:42:06Z | - |
dc.date.available | 2024-03-13T08:42:06Z | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Gut, 2022, v. 71, n. 6, p. 1106-1116 | - |
dc.identifier.issn | 0017-5749 | - |
dc.identifier.uri | http://hdl.handle.net/10722/341348 | - |
dc.description.abstract | Objective: The gut microbiota plays a key role in modulating host immune response. We conducted a prospective, observational study to examine gut microbiota composition in association with immune responses and adverse events in adults who have received the inactivated vaccine (CoronaVac; Sinovac) or the mRNA vaccine (BNT162b2; BioNTech; Comirnaty). Design: We performed shotgun metagenomic sequencing in stool samples of 138 COVID-19 vaccinees (37 CoronaVac and 101 BNT162b2 vaccinees) collected at baseline and 1 month after second dose of vaccination. Immune markers were measured by SARS-CoV-2 surrogate virus neutralisation test and spike receptor-binding domain IgG ELISA. Results: We found a significantly lower immune response in recipients of CoronaVac than BNT162b2 vaccines (p<0.05). Bifidobacterium adolescentis was persistently higher in subjects with high neutralising antibodies to CoronaVac vaccine (p=0.023) and their baseline gut microbiome was enriched in pathways related to carbohydrate metabolism (linear discriminant analysis (LDA) scores >2 and p<0.05). Neutralising antibodies in BNT162b2 vaccinees showed a positive correlation with the total abundance of bacteria with flagella and fimbriae including Roseburia faecis (p=0.028). The abundance of Prevotella copri and two Megamonas species were enriched in individuals with fewer adverse events following either of the vaccines indicating that these bacteria may play an anti-inflammatory role in host immune response (LDA scores>3 and p<0.05). Conclusion: Our study has identified specific gut microbiota markers in association with improved immune response and reduced adverse events following COVID-19 vaccines. Microbiota-targeted interventions have the potential to complement effectiveness of COVID-19 vaccines. | - |
dc.language | eng | - |
dc.relation.ispartof | Gut | - |
dc.title | Gut microbiota composition is associated with SARS-CoV- 2 vaccine immunogenicity and adverse events | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1136/gutjnl-2021-326563 | - |
dc.identifier.pmid | 35140064 | - |
dc.identifier.scopus | eid_2-s2.0-85126224389 | - |
dc.identifier.volume | 71 | - |
dc.identifier.issue | 6 | - |
dc.identifier.spage | 1106 | - |
dc.identifier.epage | 1116 | - |
dc.identifier.eissn | 1468-3288 | - |
dc.identifier.isi | WOS:000754021900001 | - |