Evidence map›Paper›PMID 29936303›Full record

ArticleClinical immunology (Orlando, Fla.)2018

Involvement of CD8+ T cell subsets in early response to vascular injury in patients with peripheral artery disease in vivo.

Pawel Maga, Tomasz P Mikolajczyk, Lukasz Partyka, Mateusz Siedlinski, Mikolaj Maga, Marek Krzanowski, Krzysztof Malinowski, Kevin Luc, Rafal Nizankowski, Deepak L Bhatt and 1 more

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. CD8Nature reviews. Cardiology · 2026
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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

11 authors at 2 institutions in 4 countries.

Pawel MagaDepartment of Angiology, Jagiellonian University Medical College, Krakow, Poland; Angio-Medcus Angiology Clinic, Krakow, Poland.
Tomasz P MikolajczykDepartment of Internal and Agricultural Medicine, Jagiellonian University Medical College, Krakow, Poland; Institute of Infection, Immunity and Inflammation, University of Glasgow, UK.
Lukasz PartykaAngio-Medcus Angiology Clinic, Krakow, Poland.
Mateusz SiedlinskiDepartment of Internal and Agricultural Medicine, Jagiellonian University Medical College, Krakow, Poland.
Mikolaj MagaDepartment of Angiology, Jagiellonian University Medical College, Krakow, Poland.
Marek KrzanowskiAngio-Medcus Angiology Clinic, Krakow, Poland.
Krzysztof MalinowskiInstitute of Public Health, Faculty of Health Sciences, Jagiellonian University Medical College, Krakow, Poland.
Kevin LucDepartment of Internal and Agricultural Medicine, Jagiellonian University Medical College, Krakow, Poland.
Rafal NizankowskiDepartment of Angiology, Jagiellonian University Medical College, Krakow, Poland.
Deepak L BhattBrigham and Women's Hospital Heart & Vascular Center, Harvard Medical School, Boston, MA, USA.
Tomasz J GuzikDepartment of Internal and Agricultural Medicine, Jagiellonian University Medical College, Krakow, Poland; Institute of Cardiovascular and Medical Sciences, University of Glasgow, UK. Electronic address: tomasz.guzik@glasgow.ac.uk.
Jagiellonian University · PLBrigham and Women's Hospital · US

Funding

British Heart Foundation RE/13/5/30177European Research Council 726318Wellcome Trust 090883
6 · The paper itself

Abstract

aimsAdaptive immunity is critical in vascular remodelling following arterial injury. We hypothesized that acute changes in T cells at a percutaneous transluminal angioplasty (PTA) site could serve as an index of their potential interaction with the injured vascular wall. METHODS AND

resultsT cell subsets were characterised in 45 patients with Rutherford 3-4 peripheral artery disease (PAD) undergoing PTA. Direct angioplasty catheter blood sampling was performed before and immediately after the procedure. PTA was associated with an acute reduction of α/β-TcR CD8+ T cells. Further characterisation revealed significant reduction in pro-atherosclerotic CD28nullCD57+ T cells, effector (CD45RA+CCR7-) and effector memory (CD45RA-CCR7-) cells, in addition to cells bearing activation (CD69, CD38) and tissue homing/adhesion markers (CD38, CCR5).

conclusionsThe acute reduction observed here is likely due to the adhesion of cells to the injured vascular wall, suggesting that immunosenescent, activated effector CD8+ cells have a role in the early vascular injury immune response following PTA in PAD patients.

Indexed as

AgedAntigens, CDCD8-Positive T-LymphocytesFemaleHumansImmunologic MemoryLeukocyte Common AntigensMalePeripheral Arterial DiseaseReceptors, Antigen, T-Cell, alpha-betaT-Lymphocyte SubsetsVascular System InjuriesAntigens, CDLeukocyte Common AntigensReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID29936303
PMCPMC6281164
OpenAlexW2809423528

What OpenQuestion holds

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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.