Evidence map›Paper›PMID 41660629›Full record

ArticleFrontiers in immunology2025

Differential composition of lymphocyte subpopulations and activation between the hypertensive Bph/2 and normotensive Bpn/3 mouse strains.

Devon Dattmore, Paiton O McDonald, Afrin Chowdhury, Saamera Awali, Allison P Boss, Yining Jin, Lisa Sather, D Adam Lauver, Cheryl E Rockwell

Abstract read
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

9 authors.

Devon DattmoreApplied Immunology Center for Education and Research, Michigan State University, East Lansing, MI, United States.
Paiton O McDonaldDepartment of Animal Science, Michigan State University, East Lansing, MI, United States.
Afrin ChowdhuryDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, United States.
Saamera AwaliDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, United States.
Allison P BossApplied Immunology Center for Education and Research, Michigan State University, East Lansing, MI, United States.
Yining JinApplied Immunology Center for Education and Research, Michigan State University, East Lansing, MI, United States.
Lisa SatherDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, United States.
D Adam LauverDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, United States.
Cheryl E RockwellApplied Immunology Center for Education and Research, Michigan State University, East Lansing, MI, United States.

Funding

The perivascular adipocyte: integrating mechanical and structural cues into vasoactive functionP01HL152951 · NHLBI · MICHIGAN STATE UNIVERSITY · PI Stephanie W Watts · 2022 to 2026
$13.3M
NHLBI NIH HHS P01 HL152951
6 · The paper itself

Abstract

Introduction: Numerous studies point to a role for the immune system in various animal models of hypertension. However, little is known about the immune system of Bph/2 mice, a spontaneously hypertensive strain. Method: To address this, we conducted a comprehensive comparison of immune cell composition and response to polyclonal T cell activation in hypertensive Bph/2 mice and normotensive Bpn/3 control mice. We quantified immune cell populations by flow cytometry from spleen and inguinal, brachial and mesenteric lymph nodes. Results: While composition of myeloid immune cell types was largely comparable between strains, we observed differences in B and T cell subpopulations. Specifically, we found an increased percentage of IgM+ IgD Conclusion/Discussion: Overall, the data suggest a decreased percentage of memory T cells in Bph/2 mice that correlates with markedly diminished proliferation and cytokine response to polyclonal activation.

Indexed as

HypertensionLymphocyte ActivationLymphocyte SubsetsAnimalsB-LymphocytesCytokinesDisease Models, AnimalMaleMiceSpleenCytokinesB cellsBph/2 micehypertensionimmune cellslymph nodesspleenT cell activationT cells

Identifiers

PMID41660629
PMCPMC12875959

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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.