Evidence map›Paper›PMID 22745375›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Multieffector-functional immune responses of HMBPP-specific Vγ2Vδ2 T cells in nonhuman primates inoculated with Listeria monocytogenes ΔactA prfA*.

Bridgett Ryan-Payseur, James Frencher, Ling Shen, Crystal Y Chen, Dan Huang, Zheng W Chen

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 67 citations in OpenAlex.

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  12. 4-1BB and cytokines trigger human NK, γδ T, and CD8Immunity, inflammation and disease · 2023
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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

6 authors at 4 institutions in 1 country.

Bridgett Ryan-PayseurDepartment of Microbiology and Immunology, Center for Primate Biomedical Research, University of Illinois College of Medicine, Chicago, IL 60612, USA.
James Frencher
Ling Shen
Crystal Y Chen
Dan Huang
Zheng W Chen
University of Illinois Urbana-Champaign · USBeth Israel Deaconess Medical Center · USIllinois College · USUniversity of Illinois Chicago · US

Funding

MODEL OF AIDS VIRUS-RELATED PULMONARY TUBERCULOSISR01HL064560 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 1999 to 2014
$9.5M
Immunotherapeutics and vaccines against anthrax, plague and tularemiaU01AI070426 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 2006 to 2010
$4.7M
SIV/MYCOBACTERIUM COINFECTIONR01RR013601 · NCRR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHEN, ZHENG W · 1998 to 2008
$4.4M
NCRR NIH HHS R01 RR013601NCRR NIH HHS RR13601NHLBI NIH HHS HL64560NHLBI NIH HHS R01 HL064560NIAID NIH HHS U01 AI070426
6 · The paper itself

Abstract

Although Listeria monocytogenes can induce systemic infection causing spontaneous abortion, septicemia, and meningitis, studies have not been performed to investigate human anti-L. monocytogenes immune responses, including those of Ag-specific Vγ2Vδ2 T cells, a dominant human γδ T cell subset. L. monocytogenes is the only pathogen known to possess both the mevalonate and non-mevalonate isoprenoid biosynthesis pathways that produce metabolic phosphates or phosphoantigens activating human Vγ2Vδ2 T cells, making it interesting to explore in vivo anti-L. monocytogenes immune responses of Vγ2Vδ2 T cells. In this study, we demonstrated that subclinical systemic L. monocytogenes infection of rhesus macaques via parenteral inoculation or vaccination with an attenuated Listeria strain induced multieffector-functional immune responses of phosphoantigen-specific Vγ2Vδ2 T cells. Subclinical systemic infection and reinfection with attenuated L. monocytogenes uncovered the ability of Vγ2Vδ2 T cells to mount expansion and adaptive or recall-like expansion. Expanded Vγ2Vδ2 T cells could traffic to and accumulate in the pulmonary compartment and intestinal mucosa. Expanded Vγ2Vδ2 T cells could evolve into effector cells producing IFN-γ, TNF-α, IL-4, IL-17, or perforin after L. monocytogenes infection, and some effector Vγ2Vδ2 T cells could coproduce IL-17 and IFN-γ, IL-4 and IFN-γ, or TNF-α and perforin. Surprisingly, in vivo-expanded Vγ2Vδ2 T effector cells in subclinical L. monocytogenes infection could directly lyse L. monocytogenes-infected target cells and inhibit intracellular L. monocytogenes bacteria. Thus, we present the first demonstration, to our knowledge, of multieffector-functional Vγ2Vδ2 T cell responses against L. monocytogenes.

Indexed as

AnimalsBacterial ProteinsCells, CulturedCytotoxicity Tests, ImmunologicEpitopes, T-LymphocyteListeria monocytogenesListeriosisMacaca mulattaMembrane ProteinsOrganophosphatesPeptide Termination FactorsReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsVaccines, Attenuated4-hydroxy-3-methyl-2-butenyl diphosphateactA protein, Listeria monocytogenesBacterial ProteinsEpitopes, T-LymphocyteMembrane ProteinsOrganophosphatesPeptide Termination FactorsPrfA protein, Listeria monocytogenesReceptors, Antigen, T-Cell, gamma-deltaVaccines, Attenuated

Identifiers

PMID22745375
PMCPMC3412419
OpenAlexW2129799990

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.