Evidence map›Paper›PMID 40073149›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2025

CD3+ T-cell: CD14+ monocyte complexes are dynamic and increased with HIV and glucose intolerance.

Laventa M Obare, Joshua Simmons, Jared Oakes, Xiuqi Zhang, Cindy Nochowicz, Stephen Priest, Samuel S Bailin, Christian M Warren, Mona Mashayekhi, Heather K Beasley and 22 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Decoding Immune Cell Doublets in Humans: From Artifacts to Insights.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2026
    Review
  3. Article
  4. Article
4 · The record

Corrections and comments

  • Update of
    CD32024
5 · Who and what money

Authors and funding

32 authors.

Laventa M ObareDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Joshua SimmonsDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Jared OakesDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0003-3910-1346
Xiuqi ZhangDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Cindy NochowiczDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Stephen PriestDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Samuel S BailinDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0003-4990-1013
Christian M WarrenVeterans Affairs Flow Cytometry Core, Veterans AffairsTennessee Valley Healthcare System, Nashville, TN, United States.
Mona MashayekhiDivision of Diabetes, Endocrinology, and Metabolism, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0003-0331-2395
Heather K BeasleyDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, United States.
Jianqiang ShaoCentral Microscopy Research Facility, University of Iowa, Iowa City, IA, United States.
Leslie M MeenderinkDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Quanhu ShengDepartment of Biostatistics, Vanderbilt University, Nashville, TN, United States.ORCID 0000-0001-8951-9295
Joey StolzeDepartment of Biostatistics, Vanderbilt University, Nashville, TN, United States.
Rama GangulaDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Tarek AbsiDepartment of Cardiac Surgery, Vanderbilt University Medical Center, Nashville, TN, United States.
Yan Ru SuDepartment of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Kit NeikirkDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, United States.
Abha ChopraInstitute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia, Australia.ORCID 0000-0001-5008-9080
Curtis L GabrielDivision of Gastroenterology, Vanderbilt University Medical Center, Nashville, TN, United States.
Tecla TemuDepartment of Global Health, University of Washington, Seattle, WA, United States.ORCID 0000-0002-0056-4143
Suman PakalaDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0001-5156-0823
Erin M WilfongDivision of Rheumatology and Immunology, Vanderbilt University Medical Center, Nashville, TN, United States.
Sara GianellaDivision of Infectious Diseases, University of California, San Diego, CA, United States.
Elizabeth J PhillipsDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0002-7623-3383
David G HarrisonDivision of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0001-9363-6451
Antentor HintonDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, United States.ORCID 0000-0002-7730-952X
Spyros A KalamsDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Annet KiraboDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, United States.ORCID 0000-0001-8580-9359
Simon A MallalDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0002-7036-1309
John R KoetheDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.
Celestine N WanjallaDivision of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID 0000-0001-9159-5414

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUSAN JANET LITTLE · 1994 to 2026
$78.4M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Stephany Norah Duda · 2015 to 2026
$27.5M
CLINICAL PHARMACOLOGY TRAINING PROGRAMT32GM007569 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Bjorn C Knollmann · 1985 to 2026
$12.4M
PRIDE: Functional and Translational Genomics of Blood DisordersR25HL106365 · NHLBI · AUGUSTA UNIVERSITY · PI PACE, BETTY SUE · 2010 to 2024
$5.2M
The Role of Adipose-Resident T Cells in HIV-Associated Glucose IntoleranceR01DK112262 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KOETHE, JOHN · 2017 to 2021
$3.8M
Immune Mechanisms of Salt-Sensitive hypertensionR01HL144941 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIRABO, ANNET · 2021 to 2025
$3.0M
Anti-cytomegalovirus Immune Responses in Atherosclerotic Cardiovascular Disease in Persons Living with HIVK23HL156759 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WANJALLA, CELESTINE N · 2021 to 2025
$860k
Immunophenotypes in the Idiopathic Inflammatory MyopathiesK08AR080808 · NIAMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Erin M Wilfong · 2022 to 2026
$818k
Bristol-Myers SquibbBurroughs Wellcome 1021480Burroughs Wellcome Fund 1021480Burroughs Wellcome Fund 1021868.01Burroughs Wellcome Fund #1022376Burroughs Wellcome Fund R01HL144941Burroughs Wellcome Fund R03HL155041Chan Zuckerberg Initiative DAFClinical Translational Science 5UL1TR002243-03CZI Science Diversity 2022- 253529Doris Duke CSDA 2021193DRTC Alzheimer's Disease Pilot & Feasibility ProgramNCATS NIH HHS UL1 TR002243NCI NIH HHS P30 CA068485NHLBI NIH HHS K23 HL156759NHLBI NIH HHS K23 HL159351NHLBI NIH HHS R01 HL144941NHLBI NIH HHS R03 HL155041NHLBI NIH HHS R25 HL106365NIAID NIH HHS P30 AI036214NIAID NIH HHS P30 AI110527NIAMS NIH HHS K08 AR080808NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK112262NIGMS NIH HHS T32 GM007569NIHNIH HHSNIH HHS DK020593Silicon Valley Community FoundationSmall Research Pilot Subaward 5R25HL106365-12Tennessee Center for AIDS Research K08AR080808Tennessee Center for AIDS Research KL2TR002245The Myositis Association Pilot AwardUNCFVanderbilt Diabetes and Research Training CenterVanderbilt Digestive Disease Research Center DK058404Vanderbilt Flow Cytometry Shared Resource
6 · The paper itself

Abstract

Persistent systemic inflammation is associated with an elevated risk of cardiometabolic diseases. However, the characteristics of the innate and adaptive immune systems in individuals who develop these conditions remain poorly defined. Doublets, or cell-cell complexes, are routinely eliminated from flow cytometric and other immune phenotyping analyses, which limits our understanding of their relationship to disease states. Using well-characterized clinical cohorts, including participants with controlled human immunodeficiency virus (HIV) as a model for chronic inflammation and increased immune cell interactions, we show that circulating CD14+ monocytes complexed to CD3+ T cells are dynamic, biologically relevant, and increased in individuals with diabetes after adjusting for confounding factors. The complexes form functional immune synapses with increased expression of proinflammatory cytokines and greater glucose utilization. Furthermore, in persons with HIV, the CD3+ T cell: CD14+ monocyte complexes had more HIV copies compared to matched CD14+ monocytes or CD4+ T cells alone. Our results demonstrate that circulating CD3+ T-cell: CD14+ monocyte pairs represent dynamic cellular interactions that may contribute to inflammation and cardiometabolic disease pathogenesis. CD3+ T-cell: CD14+ monocyte complexes may originate or be maintained, in part, by chronic viral infections. These findings provide a foundation for future studies investigating mechanisms linking T cell-monocyte cell-cell complexes to developing immune-mediated diseases, including HIV and diabetes.

Indexed as

CD3 ComplexGlucose IntoleranceHIV InfectionsLipopolysaccharide ReceptorsMonocytesT-LymphocytesAdultCell CommunicationCytokinesFemaleHumansInflammationMaleMiddle AgedCD14 protein, humanCD3 ComplexCytokinesLipopolysaccharide ReceptorsCD3+diabetesdoubletsHIVmonocyte complexesreservoirT-cell: CD14+

Identifiers

PMID40073149
PMCPMC11952877

What OpenQuestion holds

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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.