File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1038/s41541-023-00745-4
- Find via
Supplementary
-
Citations:
- Appears in Collections:
Article: COVID-19 mRNA vaccine-mediated antibodies in human breast milk and their association with breast milk microbiota composition
Title | COVID-19 mRNA vaccine-mediated antibodies in human breast milk and their association with breast milk microbiota composition |
---|---|
Authors | |
Issue Date | 5-Oct-2023 |
Publisher | Springer Nature in partnership with the Sealy Center for Vaccine Development |
Citation | NPJ vaccines., 2023, v. 8 How to Cite? |
Abstract | Newborns can acquire immunological protection to SARS-CoV-2 through vaccine-conferred antibodies in human breast milk. However, there are some concerns around lactating mothers with regards to potential short- and long-term adverse events and vaccine-induced changes to their breast milk microbiome composition, which helps shape the early-life microbiome. Thus, we sought to explore if SARS-CoV-2 mRNA vaccine could change breast milk microbiota and how the changes impact the levels of antibodies in breast milk. We recruited 49 lactating mothers from Hong Kong who received two doses of BNT162b2 vaccine between June 2021 and August 2021. Breast milk samples were self-collected by participants pre-vaccination, one week post-first dose, one week post-second dose, and one month post-second dose. The levels of SARS-CoV-2 spike-specific IgA and IgG in breast milk peaked at one week post-second dose. Subsequently, the levels of both antibodies rapidly waned in breast milk, with IgA levels returning to baseline levels one month post-second dose. The richness and composition of human breast milk microbiota changed dynamically throughout the vaccination regimen, but the abundances of beneficial microbes such as Bifidobacterium species did not significantly change after vaccination. Additionally, we found that baseline breast milk bacterial composition can predict spike-specific IgA levels at one week post-second dose (Area Under Curve: 0.72, 95% confidence interval: 0.58-0.85). Taken together, our results identified specific breast milk microbiota markers associated with high levels of IgA in the breast milk following BNT162b2 vaccine. Furthermore, in lactating mothers, BNT162b2 vaccines did not significantly reduce probiotic species in breast milk. |
Persistent Identifier | http://hdl.handle.net/10722/338312 |
ISSN | 2023 Impact Factor: 6.9 2023 SCImago Journal Rankings: 2.127 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhao, Shilin | - |
dc.contributor.author | Lok, Kris Y W | - |
dc.contributor.author | Sin, Zhen Y | - |
dc.contributor.author | Peng, Ye | - |
dc.contributor.author | Fan, Heidi S L | - |
dc.contributor.author | Nagesh, Nitya | - |
dc.contributor.author | Choi, Martha S L | - |
dc.contributor.author | Kwok, Jojo Y Y | - |
dc.contributor.author | Choi, Edmond P H | - |
dc.contributor.author | Zhang, Xi | - |
dc.contributor.author | Wai, Hogan Kok-Fung | - |
dc.contributor.author | Tsang, Leo C H | - |
dc.contributor.author | Cheng, Samuel S M | - |
dc.contributor.author | Wong, Matthew K L | - |
dc.contributor.author | Zhu, Jie | - |
dc.contributor.author | Mok, Chris K P | - |
dc.contributor.author | Ng, Siew C | - |
dc.contributor.author | Chan, Francis K L | - |
dc.contributor.author | Peiris, Malik | - |
dc.contributor.author | Poon, Leo L M | - |
dc.contributor.author | Tun, Hein M | - |
dc.date.accessioned | 2024-03-11T10:27:56Z | - |
dc.date.available | 2024-03-11T10:27:56Z | - |
dc.date.issued | 2023-10-05 | - |
dc.identifier.citation | NPJ vaccines., 2023, v. 8 | - |
dc.identifier.issn | 2059-0105 | - |
dc.identifier.uri | http://hdl.handle.net/10722/338312 | - |
dc.description.abstract | <p>Newborns can acquire immunological protection to SARS-CoV-2 through vaccine-conferred antibodies in human breast milk. However, there are some concerns around lactating mothers with regards to potential short- and long-term adverse events and vaccine-induced changes to their breast milk microbiome composition, which helps shape the early-life microbiome. Thus, we sought to explore if SARS-CoV-2 mRNA vaccine could change breast milk microbiota and how the changes impact the levels of antibodies in breast milk. We recruited 49 lactating mothers from Hong Kong who received two doses of BNT162b2 vaccine between June 2021 and August 2021. Breast milk samples were self-collected by participants pre-vaccination, one week post-first dose, one week post-second dose, and one month post-second dose. The levels of SARS-CoV-2 spike-specific IgA and IgG in breast milk peaked at one week post-second dose. Subsequently, the levels of both antibodies rapidly waned in breast milk, with IgA levels returning to baseline levels one month post-second dose. The richness and composition of human breast milk microbiota changed dynamically throughout the vaccination regimen, but the abundances of beneficial microbes such as Bifidobacterium species did not significantly change after vaccination. Additionally, we found that baseline breast milk bacterial composition can predict spike-specific IgA levels at one week post-second dose (Area Under Curve: 0.72, 95% confidence interval: 0.58-0.85). Taken together, our results identified specific breast milk microbiota markers associated with high levels of IgA in the breast milk following BNT162b2 vaccine. Furthermore, in lactating mothers, BNT162b2 vaccines did not significantly reduce probiotic species in breast milk.</p> | - |
dc.language | eng | - |
dc.publisher | Springer Nature in partnership with the Sealy Center for Vaccine Development | - |
dc.relation.ispartof | NPJ vaccines. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | COVID-19 mRNA vaccine-mediated antibodies in human breast milk and their association with breast milk microbiota composition | - |
dc.type | Article | - |
dc.identifier.doi | 10.1038/s41541-023-00745-4 | - |
dc.identifier.volume | 8 | - |
dc.identifier.eissn | 2059-0105 | - |