Evidence map›Paper›PMID 41054306›Full record

ArticleImmunology and cell biology

Myeloid cell recruitment and activation through systemic and mucosae-directed cytokine therapy.

Cordelia Manickam, Rhianna Jones, Nihar R Deb Adhikary, Kyle W Kroll, Karen Terry, Harikrishnan Balachandran, Griffin Woolley, Georgia D Tomaras, François J Villinger, R Keith Reeves

Abstract read
In one paragraph

Article in Immunology and cell biology. 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.

  1. Article
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

10 authors.

Cordelia ManickamDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.
Rhianna JonesDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.
Nihar R Deb AdhikaryNew Iberia Research Center, University of Louisiana at Lafayette, Lafayette, LA, USA.
Kyle W KrollDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.
Karen TerryDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.
Harikrishnan BalachandranDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.
Griffin WoolleyDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.
Georgia D TomarasDepartment of Surgery, Duke University School of Medicine, Durham, NC, USA.
François J VillingerNew Iberia Research Center, University of Louisiana at Lafayette, Lafayette, LA, USA.
R Keith ReevesDivision of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University School of Medicine, Durham, NC, USA.ORCID https://orcid.org/0000-0003-3157-2557

Funding

Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
Structure-Function Analytics CoreP01AI162242 · NIAID · DUKE UNIVERSITY · PI TOMARAS, GEORGIA DORIS · 2021 to 2025
$22.2M
Fine Mechanisms of Adaptive NK Cell Formation Against HIV and SIVR01AI161010 · NIAID · DUKE UNIVERSITY · PI JOST, STEPHANIE, REEVES, ROGER KEITH · 2021 to 2025
$4.9M
Resource for Nonhuman Primate Immune ReagentsR24OD010947 · OD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI VILLINGER, FRANCOIS J · 2012 to 2025
$4.9M
Role of eosinophils in SIV infectionR21AI172030 · NIAID · DUKE UNIVERSITY · PI MANICKAM, CORDELIA, REEVES, ROGER KEITH · 2022 to 2023
$443k
NIAID NIH HHS P01 AI162242NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI161010NIAID NIH HHS R21 AI172030NIH HHS P01AI162242NIH HHS P30AI064518NIH HHS R01AI161010NIH HHS R24 OD010947NIH HHS R24OD010947
6 · The paper itself

Abstract

Myeloid cells play critical roles as Fc effector cells in antibody-mediated immunity. Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a pleiotropic cytokine that promotes the recruitment and activation of multiple myeloid populations and has been used in combination with vaccines/treatments against infectious diseases, inflammatory conditions and cancers. To evaluate GM-CSF-mediated kinetics of immune cell expansion and immune outcomes, we compared subcutaneous (subQ) and topical hypoosmolar (intravaginal/intrarectal) administration in vivo using rhesus macaques (RM), as they provide easy access to longitudinal mucosal tissue sampling and are a critical model species for vaccines/therapeutics development. While topical GM-CSF did not result in a major change, neutrophils, eosinophils and monocytes were elevated within 1-3 days of subQ GM-CSF administration, with peak eosinophil and neutrophil enrichment in blood at days 7 and 8, respectively. Corresponding elevations of neutrophils, eosinophils, total CD64

Indexed as

CytokinesGranulocyte-Macrophage Colony-Stimulating FactorMucous MembraneMyeloid CellsAnimalsEosinophilsFemaleMacaca mulattaNeutrophilsVaginaCytokinesGranulocyte-Macrophage Colony-Stimulating FactorGM‐CSFmucosal immunitymyeloid cellrhesus macaques

Identifiers

PMID41054306
PMCPMC12667110

What OpenQuestion holds

Textmetadata
LicenceTDM
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.