Evidence map›Paper›PMID 20427767›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Cytotoxic potential of lung CD8(+) T cells increases with chronic obstructive pulmonary disease severity and with in vitro stimulation by IL-18 or IL-15.

Christine M Freeman, MeiLan K Han, Fernando J Martinez, Susan Murray, Lyrica X Liu, Stephen W Chensue, Timothy J Polak, Joanne Sonstein, Jill C Todt, Theresa M Ames and 5 more

5 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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.

NCT00281190 completednot on this map

Innate and Adaptive Immunity in COPD Exacerbations: Clinically-Indicated Bronchoscopies

TypeobservationalSponsorUniversity of MichiganRan2005 to 2014Enrolled32ConditionsPulmonary Disease, Chronic Obstructive, Lung Diseases, ObstructiveArmsBlood drawing, Bronchoalveolar lavage during indicated bronchoscopy
NCT00281203 completednot on this map

Innate and Adaptive Immunity in COPD Exacerbations: Bronchoscopies on Healthy Volunteers

TypeobservationalSponsorUniversity of MichiganRan2005 to 2010Enrolled32ConditionsPulmonary Disease, Chronic Obstructive, Lung Diseases, ObstructiveArmsblood drawing, fiberoptic bronchoscopy
NCT00281216 completednot on this map

Innate and Adaptive Immunity in COPD Exacerbations: Prospective Cohort Study

TypeobservationalSponsorUniversity of MichiganRan2005 to 2010Enrolled10ConditionsPulmonary Disease, Chronic Obstructive, Lung Diseases, Lung Diseases, Obstructive
NCT00281229 completednot on this map

Innate and Adaptive Immunity in COPD Exacerbations: Surgical Volunteers

TypeobservationalSponsorUniversity of MichiganRan2005 to 2015Enrolled481ConditionsPulmonary Disease, Chronic Obstructive, Lung Diseases, Obstructive
NCT00281242 completednot on this map

Innate and Adaptive Immunity in COPD Exacerbations: Severe AE-COPD Clinical Course Study

TypeobservationalSponsorUniversity of MichiganRan2005 to 2010Enrolled37ConditionsPulmonary Disease, Chronic Obstructive, Lung Diseases, ObstructiveArmsblood draw
3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 129 citations in OpenAlex.

  1. The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
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15 more citing papers are in PubMed but not listed here.

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

15 authors at 3 institutions in 1 country.

Christine M FreemanPulmonary and Critical Care Medicine Section, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI, 48105-2303, USA.
MeiLan K Han
Fernando J Martinez
Susan Murray
Lyrica X Liu
Stephen W Chensue
Timothy J Polak
Joanne Sonstein
Jill C Todt
Theresa M Ames
Douglas A Arenberg
Catherine A Meldrum
Christi Getty
Lisa McCloskey
Jeffrey L Curtis
University of Michigan · USPulmonary and Critical Care Associates · USUniversity Health System · US

Funding

PULMONARY CELLULAR AND MOLECULAR BIOLOGY TRAININGT32HL007749 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Pickett Dickson · 1993 to 2026
$19.9M
Michigan Institute for Clinical and Health Research (MICHR) (KL2)KL2RR024987 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHANLEY, THOMAS P. · 2007 to 2011
$2.8M
Innate and adaptive immunity in COPD exacerbationsR01HL082480 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CURTIS, JEFFREY LOUIS · 2005 to 2009
$2.4M
PREDICTING RESPONSE TO THERAPY IN IDIOPATHIC PULMONARY FK24HL004212 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARTINEZ, FERNANDO J · 2000 to 2009
$1.2M
NCI NIH HHS P30 CA46952NCRR NIH HHS KL2 RR024987NHLBI NIH HHS K24 HL004212NHLBI NIH HHS K24 HL04212NHLBI NIH HHS N01 HR046162NHLBI NIH HHS R01 HL082480NHLBI NIH HHS T32 HL007749NHLBI NIH HHS T32 HL07749
6 · The paper itself

Abstract

Lung CD8(+) T cells might contribute to progression of chronic obstructive pulmonary disease (COPD) indirectly via IFN-gamma production or directly via cytolysis, but evidence for either mechanism is largely circumstantial. To gain insights into these potential mechanisms, we analyzed clinically indicated lung resections from three human cohorts, correlating findings with spirometrically defined disease severity. Expression by lung CD8(+) T cells of IL-18R and CD69 correlated with severity, as did mRNA transcripts for perforin and granzyme B, but not Fas ligand. These correlations persisted after correction for age, smoking history, presence of lung cancer, recent respiratory infection, or inhaled corticosteroid use. Analysis of transcripts for killer cell lectin-like receptor G1, IL-7R, and CD57 implied that lung CD8(+) T cells in COPD do not belong to the terminally differentiated effector populations associated with chronic infections or extreme age. In vitro stimulation of lung CD8(+) T cells with IL-18 plus IL-12 markedly increased production of IFN-gamma and TNF-alpha, whereas IL-15 stimulation induced increased intracellular perforin expression. Both IL-15 and IL-18 protein expression could be measured in whole lung tissue homogenates, but neither correlated in concentration with spirometric severity. Although lung CD8(+) T cell expression of mRNA for both T-box transcription factor expressed in T cells and GATA-binding protein 3 (but not retinoic acid receptor-related orphan receptor gamma or alpha) increased with spirometric severity, stimulation of lung CD8(+) T cells via CD3epsilon-induced secretion of IFN-gamma, TNF-alpha, and GM-CSF, but not IL-5, IL-13, and IL-17A. These findings suggest that the production of proinflammatory cytokines and cytotoxic molecules by lung-resident CD8(+) T cells contributes to COPD pathogenesis.

Indexed as

AgedAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCD8-Positive T-LymphocytesCell SeparationCytokinesCytotoxicity, ImmunologicFemaleFlow CytometryForced Expiratory VolumeHumansInterleukin-15Interleukin-18Lectins, C-TypeMaleAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCytokinesInterleukin-15Interleukin-18Lectins, C-TypeRNA, Messenger

Identifiers

PMID20427767
PMCPMC4098931
OpenAlexW2150445188

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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.