Evidence map›Paper›PMID 28620373›Full record

ReviewFrontiers in immunology2017

Mechanisms of Autoantibody-Induced Pathology.

Ralf J Ludwig, Karen Vanhoorelbeke, Frank Leypoldt, Ziya Kaya, Katja Bieber, Sandra M McLachlan, Lars Komorowski, Jie Luo, Otavio Cabral-Marques, Christoph M Hammers and 14 more

Registry-linked trialAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03621605 (A Phase 1 Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety and Tolerability of Single and Multiple Ascending Doses of VIB9600 by Intravenous Infusion or Subcutaneous Injection in Healthy Subjects), which is not on this map. Cited by 265 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
265citing papers in PubMed, 5 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.

NCT03621605 phase1terminatednot on this mapstarted 2018, after this paper: background citation

A Phase 1 Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety and Tolerability of Single and Multiple Ascending Doses of VIB9600 by Intravenous Infusion or Subcutaneous Injection in Healthy Subjects

TypeinterventionalSponsorAmgenRan2018 to 2019Enrolled24ConditionsSafety IssuesArmsVIB9600, Placebos
3 · Its place in the literature

Who cites it

265 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Article
  11. β1 Autoantibodies Stimulate T Cells to Become Cardiotoxic.JACC. Basic to translational science · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Distributed Clonal Deletion Prevents Autoimmune Disease Progression.bioRxiv : the preprint server for biology · 2026
    Article
  17. Review
  18. Article
  19. Review
  20. Article

205 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

24 authors.

Ralf J LudwigLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Karen VanhoorelbekeLaboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.
Frank LeypoldtNeuroimmunology, Institute of Clinical Chemistry, University Hospital Schleswig-Holstein, Kiel, Germany.
Ziya KayaDepartment of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
Katja BieberLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Sandra M McLachlanThyroid Autoimmune Disease Unit, Cedars-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA, United States.
Lars KomorowskiInstitute for Experimental Immunology, Affiliated to Euroimmun AG, Lübeck, Germany.
Jie LuoDepartment of Neuroscience, University of Pennsylvania Medical School, Philadelphia, PA, United States.
Otavio Cabral-MarquesDepartment of Rheumatology, University of Lübeck, Lübeck, Germany.
Christoph M HammersDepartment of Dermatology, University of Lübeck, Lübeck, Germany.
Jon M LindstromDepartment of Neuroscience, University of Pennsylvania Medical School, Philadelphia, PA, United States.
Peter LamprechtDepartment of Rheumatology, University of Lübeck, Lübeck, Germany.
Andrea FischerDepartment of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
Gabriela RiemekastenDepartment of Rheumatology, University of Lübeck, Lübeck, Germany.
Claudia TersteegLaboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.
Peter SondermannSuppreMol GmbH, Martinsried, Germany.
Basil RapoportThyroid Autoimmune Disease Unit, Cedars-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA, United States.
Klaus-Peter WandingerDepartment of Neurology, Institute of Clinical Chemistry, University Medical-Centre Schleswig-Holstein, Lübeck, Germany.
Christian ProbstInstitute for Experimental Immunology, Affiliated to Euroimmun AG, Lübeck, Germany.
Asmaa El BeidaqInstitute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.
Enno SchmidtLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Alan VerkmanDepartment of Medicine, University of California, San Francisco, CA, United States.
Rudolf A ManzInstitute for Systemic Inflammation Research, University of Lübeck, Lübeck, Germany.
Falk NimmerjahnDepartment of Biology, Institute of Genetics, University of Erlangen-Nuremberg, Erlangen, Germany.

Funding

Functional Role of Aquaporins in Eye PhysiologyR01EY013574 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VERKMAN, ALAN S · 2002 to 2022
$7.6M
THYROTROPIN RECEPTOR IN HEALTH AND DISEASER01DK019289 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI RAPOPORT, BASIL · 1986 to 2014
$6.1M
MODULATION OF AN ANIMAL MODEL OF HYPERTHYROIDISMR01DK054684 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI MCLACHLAN, SANDRA M · 1999 to 2017
$5.6M
NEI NIH HHS R01 EY013574NIDDK NIH HHS R01 DK019289NIDDK NIH HHS R01 DK054684
6 · The paper itself

Abstract

Autoantibodies are frequently observed in healthy individuals. In a minority of these individuals, they lead to manifestation of autoimmune diseases, such as rheumatoid arthritis or Graves' disease. Overall, more than 2.5% of the population is affected by autoantibody-driven autoimmune disease. Pathways leading to autoantibody-induced pathology greatly differ among different diseases, and autoantibodies directed against the same antigen, depending on the targeted epitope, can have diverse effects. To foster knowledge in autoantibody-induced pathology and to encourage development of urgently needed novel therapeutic strategies, we here categorized autoantibodies according to their effects. According to our algorithm, autoantibodies can be classified into the following categories: (1) mimic receptor stimulation, (2) blocking of neural transmission, (3) induction of altered signaling, triggering uncontrolled (4) microthrombosis, (5) cell lysis, (6) neutrophil activation, and (7) induction of inflammation. These mechanisms in relation to disease, as well as principles of autoantibody generation and detection, are reviewed herein.

Indexed as

autoantibodiesautoimmunityB cellsdiagnosismouse modelspathogenesistreatment

Identifiers

PMID28620373
PMCPMC5449453

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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.