Evidence map›Paper›PMID 37074206›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

Natural Microbial Exposure from the Earliest Natural Time Point Enhances Immune Development by Expanding Immune Cell Progenitors and Mature Immune Cells.

Sarah Burger, Terran Stenger, Mark Pierson, Adhvaith Sridhar, Matthew A Huggins, Tamara A Kucaba, Thomas S Griffith, Sara E Hamilton, Nathaniel J Schuldt

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

16 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. A gavage-fomite based method to generate mouse models with natural microbiota.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  3. Article
  4. Article
  5. CXCL10 Regulates Pressure Overload-Induced Heart Failure.JACC. Basic to translational science · 2026
    Article
  6. Article
  7. Article
  8. Guardians within: Cross-talk between the gut microbiome and host immune system.World journal of gastrointestinal pathophysiology · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. CD115Cell reports · 2023
    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

9 authors at 1 institution in 1 country.

Sarah BurgerCenter for Immunology, University of Minnesota, Minneapolis, MN.
Terran StengerCenter for Immunology, University of Minnesota, Minneapolis, MN.ORCID 0000-0002-8199-0880
Mark PiersonCenter for Immunology, University of Minnesota, Minneapolis, MN.
Adhvaith SridharCenter for Immunology, University of Minnesota, Minneapolis, MN.
Matthew A HugginsCenter for Immunology, University of Minnesota, Minneapolis, MN.
Tamara A KucabaDepartment of Urology, University of Minnesota, Minneapolis, MN.
Thomas S GriffithCenter for Immunology, University of Minnesota, Minneapolis, MN.ORCID 0000-0002-7205-9859
Sara E HamiltonCenter for Immunology, University of Minnesota, Minneapolis, MN.ORCID 0000-0002-3768-7622
Nathaniel J SchuldtCenter for Immunology, University of Minnesota, Minneapolis, MN.ORCID 0000-0001-7692-4814
University of Minnesota · US

Funding

Understanding the functional agility of effector memory CD8 T cellsR01AI155468 · NIAID · UNIVERSITY OF MINNESOTA · PI HAMILTON HART, SARA ELIZABETH · 2021 to 2025
$2.8M
CD4 T cell dysregulation and reprogramming in sepsisR35GM140881 · NIGMS · UNIVERSITY OF MINNESOTA · PI Thomas S Griffith · 2021 to 2026
$2.4M
Using microbially-experienced mice to study the innate immune response in sepsisI01BX001324 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI GRIFFITH, THOMAS S · 2013 to 2025
–
BLRD Research Career Scientist Award ApplicationIK6BX006192 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI Thomas S Griffith · 2023 to 2026
–
BLRD VA I01 BX001324BLRD VA IK6 BX006192NIAID NIH HHS R01 AI155468NIGMS NIH HHS R35 GM140881
6 · The paper itself

Abstract

Microbial experience fundamentally shapes immunity, particularly during the perinatal period when the immune system is underdeveloped, and novel microbial encounters are common. Most animal models are raised in specific pathogen-free (SPF) conditions with relatively uniform microbial communities. How SPF housing conditions alter early-life immune development relative to natural microbial exposure (NME) has not been thoroughly investigated. In this article, we compare immune development in SPF-raised mice with mice born from immunologically experienced mothers in microbially diverse environments. NME induced broad immune cell expansion, including naive cells, suggesting mechanisms besides activation-induced proliferation contribute to the increase in immune cell numbers. We found NME conditions also expanded immune cell progenitor cell populations in the bone marrow, suggesting microbial experience enhances immune development at the earliest stages of immune cell differentiation. Multiple immune functions characteristically impaired in infants were also enhanced by NME, including T cell memory and Th1 polarization, B cell class switching and Ab production, proinflammatory cytokine expression, and bacterial clearance after Listeria monocytogenes challenge. Collectively, our studies reveal numerous impairments in immune development in SPF conditions relative to natural immune development.

Indexed as

CytokinesListeria monocytogenesAnimalsB-LymphocytesBone MarrowMiceMice, Inbred C57BLStem CellsCytokines

Identifiers

PMID37074206
PMCPMC10192123
OpenAlexW4366352885

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.