Evidence map›Paper›PMID 34421900›Full record

ArticleFrontiers in immunology2021

sCD28, sCD80, sCTLA-4, and sBTLA Are Promising Markers in Diagnostic and Therapeutic Approaches for Aseptic Loosening and Periprosthetic Joint Infection.

Jil M Jubel, Thomas M Randau, Janine Becker-Gotot, Sebastian Scheidt, Matthias D Wimmer, Hendrik Kohlhof, Christof Burger, Dieter C Wirtz, Frank A Schildberg

Abstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Novel diagnostic markers for periprosthetic joint infection: a systematic review.Frontiers in cellular and infection microbiology · 2023
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

9 authors.

Jil M JubelClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Thomas M RandauClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Janine Becker-GototInstitute of Experimental Immunology, University Hospital Bonn, Bonn, Germany.
Sebastian ScheidtClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Matthias D WimmerClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Hendrik KohlhofClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Christof BurgerClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Dieter C WirtzClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Frank A SchildbergClinic for Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aseptic prosthetic loosening and periprosthetic joint infections (PJI) are among the most frequent complications after total knee/hip joint arthroplasty (TJA). Current research efforts focus on understanding the involvement of the immune system in these frequent complications. Different immune cell types have already been implicated in aseptic prosthetic loosening and PJI. The aim of this study was to systematically analyze aspirates from knee and hip joints, evaluating the qualitative and quantitative composition of soluble immunoregulatory markers, with a focus on co-inhibitory and co-stimulatory markers. It has been shown that these molecules play important roles in immune regulation in cancer and chronic infectious diseases, but they have not been investigated in the context of joint replacement. For this purpose, aspirates from control joints (i.e., native joints without implanted prostheses), joints with TJA (no signs of infection or aseptic loosening), joints with aseptic implant failure (AIF; i.e., aseptic loosening), and joints with PJI were collected. Fourteen soluble immunoregulatory markers were assessed using bead-based multiplex assays. In this study, it could be shown that the concentrations of the analyzed immunoregulatory molecules vary between control, TJA, AIF, and PJI joints. Comparing TJA patients to CO patients, sCD80 was significantly elevated. The marker sBTLA was significantly elevated in AIF joints compared to TJA joints. In addition, a significant difference for eight markers could be shown when comparing the AIF and CO groups (sCD27, sCTLA-4, sCD137, sCD80, sCD28, sTIM-3, sPD-1, sBTLA). A significant difference was also reached for nine soluble markers when the PJI and CO groups were compared (sLAG-3, sCTLA-4, sCD27, sCD80, sCD28, sTIM-3, sPD-1, IDO, sBTLA). In summary, the analyzed immunoregulatory markers could be useful for diagnostic purposes as well as to develop new therapeutic approaches for AIF and PJI.

Indexed as

Prosthesis FailureAdultAgedAged, 80 and overArthroplasty, Replacement, HipArthroplasty, Replacement, KneeB7-1 AntigenBiomarkersCD28 AntigensCTLA-4 AntigenFemaleHumansJoint ProsthesisMaleMiddle AgedProsthesis-Related InfectionsB7-1 AntigenBiomarkersCD28 AntigensCTLA-4 AntigenReceptors, Immunologicaseptic looseningimmunoregulatory markersosteoimmunologyperiprosthetic joint infectionsBTLAsCD28sCD80sCTLA-4

Identifiers

PMID34421900
PMCPMC8377391

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.