Evidence map›Paper›PMID 34665695›Full record

ArticleClinical and experimental rheumatology2022

Autoantibodies against the envelope proteins of endogenous retroviruses K102 and K108 in patients with systemic lupus erythematosus correlate with active disease.

Anastasia I Khadjinova, Xiaoxing Wang, Amanda Laine, Kennedy Ukadike, Mary Eckert, Anne Stevens, Anders A Bengtsson, Christian Lood, Tomas Mustelin

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental rheumatology, 2022. 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
2.4field-weighted citation impact, top 10% 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, 28 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Microorganisms · 2024
    Review
  10. Article
  11. Article
  12. Autoimmunity: the neoantigen hypothesis.Frontiers in immunology · 2024
    Article
  13. Article
  14. Article
  15. 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 at 3 institutions in 2 countries.

Anastasia I KhadjinovaDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA.
Xiaoxing WangDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA.
Amanda LaineDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA.
Kennedy UkadikeDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA.
Mary EckertSeattle Children's Hospital, Seattle, WA, USA.
Anne StevensSeattle Children's Hospital and Seattle Children's Research Institute, Seattle, WA, and Jansen Research and Development LLC, Malvern, PA, USA.
Anders A BengtssonDepartment of Rheumatology, Lund University, Lund, Sweden.
Christian LoodDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA.
Tomas MustelinDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA. tomas2@uw.edu.
University of Washington · USLund University · SESeattle Children's Hospital · US

Funding

RESEARCH TRAINING IN RHEUMATOLOGYT32AR007108 · NIAMS · UNIVERSITY OF WASHINGTON · PI Shaun Jackson, Tomas M Mustelin · 1986 to 2026
$6.6M
Role of protein citrullination in rheumatoid arthritisR01AR074939 · NIAMS · UNIVERSITY OF WASHINGTON · PI MUSTELIN, TOMAS M · 2020 to 2024
$1.9M
The roots of SLE: Can we cure it with a reverse transcriptase inhibitor?R21AR075134 · NIAMS · UNIVERSITY OF WASHINGTON · PI MUSTELIN, TOMAS M · 2019 to 2020
$427k
HERV-K immunity, a trigger of citrullination in rheumatoid arthritis?R21AR077266 · NIAMS · UNIVERSITY OF WASHINGTON · PI MUSTELIN, TOMAS M · 2021 to 2022
$425k
NIAMS NIH HHS R01 AR074939NIAMS NIH HHS R21 AR075134NIAMS NIH HHS R21 AR077266NIAMS NIH HHS T32 AR007108
6 · The paper itself

Abstract

objectivesTo determine if patients with systemic lupus erythematosus (SLE), a disease characterised by elevated type I interferons reminiscent of anti-viral immunity, have expression of human endogenous retrovirus K (HERV-K) proviruses capable of producing envelope (Env) protein, as well as associated autoantibodies against the Env protein.

methodsELISAs were conducted with recombinant Env protein and sera from SLE patients with active (n=60) or inactive (n=49) disease, healthy controls (n=47), other rheumatic disorders (n=59), as well as plasma from paediatric lupus patients with active (n=30) or inactive (n=30) disease, and 17 healthy children. Antibody reactivity was evaluated for correlations with clinical and laboratory parameters of the patients. Expression of HERV-K transcripts were profiled in SLE leukocytes by RNA-Seq.

resultsBoth adult and paediatric SLE patients had autoantibodies against HERV-K Env with higher titres than healthy controls or patients with Sjögren's syndrome, small- or large-vessel vasculitis, or psoriatic arthritis. Transcripts from only two HERV-K loci capable of producing Env, HERV-K102 and -K108, were detected among the 10 expressed loci in SLE patients.

conclusionsOur data reveal that HERV-K proviruses are expressed in SLE and that the HERV-K-encoded Env protein elicits an immune response in patients, particularly during active disease.

Indexed as

Endogenous RetrovirusesLupus Erythematosus, SystemicAdultAutoantibodiesChildEnzyme-Linked Immunosorbent AssayGene Products, envHumansAutoantibodiesGene Products, env

Identifiers

PMID34665695
PMCPMC10695298
OpenAlexW3205079829

What OpenQuestion holds

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Registered trials

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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.