Evidence map›Paper›PMID 40259466›Full record

ArticleClinical and experimental immunology2025

Prospective analysis of the number and function of two T regulatory cell subsets in healthy individuals.

Erick Colunga-Bolaños, Lesly Doniz-Padilla, Marlen Vitales-Noyola, Larisa González-Baranda, Berenice Hernández-Castro, Perla Niño-Moreno, Diana P Portales-Pérez, Roberto González-Amaro

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Article in Clinical and experimental 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.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Erick Colunga-BolañosResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.
Lesly Doniz-PadillaResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.
Marlen Vitales-NoyolaResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.
Larisa González-BarandaResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.
Berenice Hernández-CastroSchool of Medicine, UASLP, San Luis Potosí, SLP, México.
Perla Niño-MorenoResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.
Diana P Portales-PérezResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.
Roberto González-AmaroResearch Center for Health Sciences and Biomedicine (CICSaB), Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México.ORCID 0000-0001-6025-7375

Funding

Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP, México
6 · The paper itself

Abstract

introductionT regulatory (Treg) cells play a crucial role in immune system homeostasis and in the pathogenesis of immune-mediated inflammatory diseases. Accordingly, numerous studies have examined the number and function of these lymphocytes in patients with different conditions as well as in healthy controls. The aim of this study was to analyze potential variations in the number and function of two Treg cell subsets in healthy adults over a 2-month period.

methodsIn a pilot study, blood samples were collected from 20 healthy individuals on Days 0, 30, and 60, and the levels of natural Treg cells (CD4+CD25highFoxp3+) and CD69+ Treg cells (CD4+CD69+CD25-/+LAP+IL-10+Foxp3-) were analyzed by flow cytometry. In addition, the function of these regulatory cells was evaluated using an in vitro assay that measures the inhibition of activation of autologous T lymphocytes.

resultsAlthough no significant differences were observed across the three serial measurements of the number or function of the Treg cells analyzed (P > 0.05 in both cases), a substantial proportion of individuals showed notable changes (either an increase or decrease) in these parameters during the study. These variations were not apparently associated with any factors affecting immune system homeostasis, including infections, medication use, or immunizations.

conclusionOur findings suggest that significant fluctuations of causes to be determined occur in the levels and function of Treg cells in healthy individuals. This phenomenon should be considered in studies investigating immunoregulation in humans.

Indexed as

T-Lymphocytes, RegulatoryT-Lymphocyte SubsetsAdultAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensFemaleFlow CytometryForkhead Transcription FactorsHealthy VolunteersHomeostasisHumansLectins, C-TypeLymphocyte ActivationLymphocyte CountMaleAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensForkhead Transcription FactorsFOXP3 protein, humanLectins, C-Typeimmune parametersimmune suppressionlymphocytesT regulatory cells

Identifiers

PMID40259466
PMCPMC12116287

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