Publication
Secretory IgA and T Cells Targeting SARS-CoV-2 Spike Protein Are Transferred to the Breastmilk Upon mRNA Vaccination
dc.contributor.author | Gonçalves, J | |
dc.contributor.author | Juliano, AM | |
dc.contributor.author | Charepe, N | |
dc.contributor.author | Alenquer, M | |
dc.contributor.author | Athayde, D | |
dc.contributor.author | Ferreira, F | |
dc.contributor.author | Archer, M | |
dc.contributor.author | Amorim, MJ | |
dc.contributor.author | Serrano, F | |
dc.contributor.author | Soares, H | |
dc.date.accessioned | 2022-01-21T15:09:44Z | |
dc.date.available | 2022-01-21T15:09:44Z | |
dc.date.issued | 2021 | |
dc.description.abstract | In view of the scarcity of data to guide decision making, we evaluated how BNT162b2 and mRNA-1273 vaccines affect the immune response in lactating women and the protective profile of breastmilk. Compared with controls, lactating women had a higher frequency of circulating RBD memory B cells and higher anti-RBD antibody titers but similar neutralizing capacity. We show that upon vaccination, immune transfer to breastmilk occurs through a combination of anti-spike secretory IgA (SIgA) antibodies and spike-reactive T cells. Although we found that the concentration of anti-spike IgA in breastmilk might not be sufficient to directly neutralize SARS-CoV-2, our data suggest that cumulative transfer of IgA might provide the infant with effective neutralization capacity. Our findings put forward the possibility that breastmilk might convey both immediate (through anti-spike SIgA) and long-lived (via spike-reactive T cells) immune protection to the infant. Further studies are needed to address this possibility and to determine the functional profile of spike T cells. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Cell Rep Med. 2021 Dec 21;2(12):100468. | pt_PT |
dc.identifier.doi | 10.1016/j.xcrm.2021.100468 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.17/3960 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Elsevier | pt_PT |
dc.subject | MAC MED MAF | pt_PT |
dc.subject | Antibodies, Viral / blood | pt_PT |
dc.subject | Antibodies, Viral / immunology | pt_PT |
dc.subject | COVID-19 / immunology | pt_PT |
dc.subject | COVID-19 / prevention & control | pt_PT |
dc.subject | COVID-19 Vaccines / immunology* | pt_PT |
dc.subject | Female | pt_PT |
dc.subject | Humans | pt_PT |
dc.subject | Immunity, Maternally-Acquired | pt_PT |
dc.subject | Immunoglobulin A, Secretory / immunology* | pt_PT |
dc.subject | Lactation / immunology | pt_PT |
dc.subject | Memory B Cells / immunology | pt_PT |
dc.subject | Milk, Human / immunology* | pt_PT |
dc.subject | SARS-CoV-2 / immunology* | pt_PT |
dc.subject | Spike Glycoprotein, Coronavirus / immunology* | pt_PT |
dc.subject | T-Lymphocytes / immunology* | pt_PT |
dc.subject | mRNA Vaccines / immunology | pt_PT |
dc.subject | Vaccination | pt_PT |
dc.title | Secretory IgA and T Cells Targeting SARS-CoV-2 Spike Protein Are Transferred to the Breastmilk Upon mRNA Vaccination | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.startPage | 100468 | pt_PT |
oaire.citation.title | Cell Reports. Medicine | pt_PT |
oaire.citation.volume | 2 | pt_PT |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |
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