Evidence map›Paper›PMID 41030442›Full record

ArticleFrontiers in immunology2025

Comparative single-cell immune responses in peripheral blood and lymph node of immunized SARS-CoV-2 challenged infant rhesus macaques.

Sasha Anronikov, Cameron Meikle, Emma C Milligan, Han Chen, Nilanjan Mukherjee, Zach Bjornson, Brice Gaudillière, Sizun Jiang, Sallie R Permar, Koen K A Van Rompay and 3 more

Abstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Sasha Anronikov *Department of Microbiology and Immunology, School of Medicine, Stanford University, Stanford, CA, United States.
Cameron Meikle *Department of Microbiology and Immunology, School of Medicine, University of Nevada, Reno, Reno, NV, United States.
Emma C MilliganDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC, United States.
Han ChenDepartment of Microbiology and Immunology, School of Medicine, Stanford University, Stanford, CA, United States.
Nilanjan MukherjeeDepartment of Microbiology and Immunology, School of Medicine, Stanford University, Stanford, CA, United States.
Zach BjornsonDepartment of Microbiology and Immunology, School of Medicine, Stanford University, Stanford, CA, United States.
Brice GaudillièreDepartment of Anesthesiology, Perioperative & Pain Medicine, Stanford University, Stanford, CA, United States.
Sizun JiangCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, United States.
Sallie R PermarDepartment of Pediatrics, Weill Cornell Medicine, New York, NY, United States.
Koen K A Van RompayCalifornia National Primate Research Center, University of California, Davis, Davis, CA, United States.
Garry P NolanDepartment of Pathology, School of Medicine, Stanford University, Stanford, CA, United States.
Kristina De ParisDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC, United States.
David R McIlwainDepartment of Microbiology and Immunology, School of Medicine, University of Nevada, Reno, Reno, NV, United States.

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
NIH HHS P51 OD011107
6 · The paper itself

Abstract

Introduction: A better understanding of post-exposure immune responses in vaccinated individuals, particularly infants, is needed. Methods: Using a rhesus macaque model, we compared recipients of mRNA- or protein-based SARS-CoV-2 vaccines administered in infancy with unvaccinated controls 7 days post-SARS-CoV-2 virus challenge. Mass cytometry profiling of peripheral blood mononuclear cells and dissociated mediastinal lymph node cells at 7 days post-challenge revealed tissue-specific differences between groups, representing a snapshot of immune activity at this point. Results: Vaccinated animals showed lower frequencies of activated CD8+ T cells in blood and lower levels of monocyte and B cell subsets in lymph nodes, aligning with lower viral loads and milder pathology. Plasmacytoid dendritic cells-commonly depleted in circulation during severe human COVID-19-were preserved in the blood of vaccinated groups. Discussion: These findings enhance our understanding of a critical nonhuman primate model and underscore the utility of single-cell, tissue-level analyses in evaluating next-generation pediatric SARS-CoV-2 vaccine strategies.

Indexed as

COVID-19COVID-19 VaccinesLymph NodesSARS-CoV-2AnimalsCD8-Positive T-LymphocytesDisease Models, AnimalFemaleHumansLeukocytes, MononuclearMacaca mulattaMaleSingle-Cell AnalysisCOVID-19 VaccinesCOVID-19CyTOFdelta variantlymph nodeperipheral blood mononuclear cellsrhesus macaquesSARS-CoV-2vaccine

Identifiers

PMID41030442
PMCPMC12477255

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.