Evidence map›Paper›PMID 29139571›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2018

Human prosthetic joint infections are associated with myeloid-derived suppressor cells (MDSCs): Implications for infection persistence.

Cortney E Heim, Debbie Vidlak, Jessica Odvody, Curtis W Hartman, Kevin L Garvin, Tammy Kielian

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
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  3. Osteomyelitis.Nature reviews. Disease primers · 2026
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  11. Immune Checkpoint Molecules as Biomarkers ofbioRxiv : the preprint server for biology · 2024
    Article
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  16. CXCR2 perturbation promotesJournal of medical microbiology · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Article
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 1 institution in 1 country.

Cortney E HeimDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, 68198-5900.
Debbie VidlakDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, 68198-5900.
Jessica OdvodyDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, 68198-5900.
Curtis W HartmanOrthopaedic Surgery and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska, 68198-5640.
Kevin L GarvinOrthopaedic Surgery and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska, 68198-5640.
Tammy KielianDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, 68198-5900.
University of Nebraska Medical Center · US

Funding

The S. aureus biofilm lifecycleP01AI083211 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAYLES, KENNETH W. · 2009 to 2023
$32.1M
NIAID NIH HHS P01 AI083211
6 · The paper itself

Abstract

Prosthetic joint infection (PJI) is a devastating complication of joint arthroplasty surgery typified by biofilm formation. Currently, mechanisms whereby biofilms persist and evade immune-mediated clearance in immune competent patients remain largely ill-defined. Therefore, the current study characterized leukocyte infiltrates and inflammatory mediator expression in tissues from patients with PJI compared to aseptic loosening. CD33 CLINICAL SIGNIFICANCE: Animal models of PJI have revealed a critical role for MDSCs and IL-10 in promoting infection persistence; however, whether this population is prevalent during human PJI and across distinct bacterial pathogens remains unknown. This study has identified that granulocytic-MDSC infiltrates are unique to human PJIs caused by distinct bacteria, which are not associated with aseptic loosening of prosthetic joints. Better defining the immune status of human PJIs could lead to novel immune-mediated approaches to facilitate PJI clearance in combination with conventional antibiotics. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:1605-1613, 2018.

Indexed as

AgedAged, 80 and overFemaleHLA-DR AntigensHumansInflammation MediatorsMaleMiddle AgedMyeloid-Derived Suppressor CellsProsthesis-Related InfectionsT-LymphocytesHLA-DR AntigensInflammation Mediatorsbiofilmmyeloid-derived suppressor cellsneutrophilsprosthetic joint infectionstaphylococci

Identifiers

PMID29139571
PMCPMC5953848
OpenAlexW2769063900

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.