Evidence map›Paper›PMID 36203549›Full record

ArticlemedRxiv : the preprint server for health sciences2022

Spike-specific T cells are enriched in breastmilk following SARS-CoV-2 mRNA vaccination.

Blair Armistead, Yonghou Jiang, Marc Carlson, Emily S Ford, Saumya Jani, John Houck, Xia Wu, Lichen Jing, Tiffany Pecor, Alisa Kachikis and 7 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. The evolution of SARS-CoV-2.Nature reviews. Microbiology · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Blair ArmisteadCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Yonghou JiangCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Marc CarlsonResearch Scientific Computing, Enterprise Analytics, Seattle Children's Research Institute; Seattle, WA, USA.
Emily S FordVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center; Seattle, WA, USA.
Saumya JaniDepartment of Medicine, University of Washington; Seattle, WA, USA.
John HouckCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Xia WuDepartment of Medicine, University of Washington; Seattle, WA, USA.
Lichen JingDepartment of Medicine, University of Washington; Seattle, WA, USA.
Tiffany PecorCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Alisa KachikisDepartment of Obstetrics & Gynecology, University of Washington; Seattle, WA, USA.
Winnie YeungCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Tina NguyenCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Nana MinkahCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Sasha E LarsenCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Rhea N ColerCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
David M KoelleVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center; Seattle, WA, USA.
Whitney E HarringtonCenter for Global Infectious Disease Research, Seattle Children's Research Institute; Seattle, WA, USA.
Center for Infectious Disease Research · USUniversity of Washington · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZASeattle Children's Hospital · US

Funding

Kaiser Washington VTEU supplement 20-0003UM1AI148373 · NIAID · KAISER FOUNDATION RESEARCH INSTITUTE · PI LISA A JACKSON · 2020 to 2026
$24.4M
Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
Large Scale T Cell Epitope Discovery: Local and Systemic T cell Response to Herpes Simplex Virus75N93019C00063 · NIAID · UNIVERSITY OF WASHINGTON · PI MYER, TIM · 2019 to 2023
$5.5M
HSV-2 specificity and phenotyping of tissue-based T cells in genital skin biopsies of HSV-2 reactivationK08AI148588 · NIAID · UNIVERSITY OF WASHINGTON · PI FORD, EMILY · 2020 to 2024
$947k
Protection of at-risk low birth weight infants against influenza via maternal antibodyK23AI153390 · NIAID · UNIVERSITY OF WASHINGTON · PI KACHIKIS, ALISA · 2021 to 2025
$942k
The Effect of Maternal Cells on Infant ImmunityK08AI135072 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI HARRINGTON, WHITNEY ELIZABETH · 2018 to 2022
$854k
C19 SARS-CoV-2-specific T cells in the infected nasel epitheliumR21AI163999 · NIAID · UNIVERSITY OF WASHINGTON · PI KOELLE, DAVID M · 2021 to 2022
$485k
NCI NIH HHS T32 CA080416NIAID NIH HHS 75N93019C00063NIAID NIH HHS K08 AI135072NIAID NIH HHS K08 AI148588NIAID NIH HHS K23 AI153390NIAID NIH HHS R21 AI163999NIAID NIH HHS T32 AI007509NIAID NIH HHS UM1 AI148373
6 · The paper itself

Abstract

Human breastmilk is rich in T cells; however, their specificity and function are largely unknown. We compared the phenotype, diversity, and antigen specificity of T cells in the breastmilk and peripheral blood of lactating individuals who received SARS-CoV-2 mRNA vaccination. Relative to blood, breastmilk contained higher frequencies of T effector and central memory populations that expressed mucosal-homing markers. T cell receptor (TCR) sequence overlap was limited between blood and breastmilk. Overabundan t breastmilk clones were observed in all individuals, were diverse, and contained CDR3 sequences with known epitope specificity including to SARS-CoV-2 Spike. Spike-specific TCRs were more frequent in breastmilk compared to blood and expanded in breastmilk following a third mRNA vaccine dose. Our observations indicate that the lactating breast contains a distinct T cell population that can be modulated by maternal vaccination with potential implications for infant passive protection. One-Sentence Summary: The breastmilk T cell repertoire is distinct and enriched for SARS-CoV-2 Spike-specificity after maternal mRNA vaccination.

Identifiers

PMID36203549
PMCPMC9536058
OpenAlexW4200294004

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.