Evidence map›Paper›PMID 32161059›Full record

ArticleImmunoHorizons2020

Type I IFN Drives Experimental Systemic Lupus Erythematosus by Distinct Mechanisms in CD4 T Cells and B Cells.

Jared Klarquist, Rachel Cantrell, Maria A Lehn, Kristin Lampe, Cassandra M Hennies, Kasper Hoebe, Edith M Janssen

Open access · goldAbstract read
In one paragraph

Article in ImmunoHorizons, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  3. Immune-Related Gene Variants as Modifiers of Multiple Sclerosis Severity.International journal of molecular sciences · 2026
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  8. BeyondInternational journal of molecular sciences · 2025
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  9. Review
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  12. B Cell Tolerance and Targeted Therapies in SLE.Journal of clinical medicine · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Regulation of B Cell Responses in SLE by Three Classes of Interferons.International journal of molecular sciences · 2021
    Review
  17. CD38 Deficiency Ameliorates Chronic Graft-Frontiers in immunology · 2021
    Article
  18. Review
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

7 authors at 3 institutions in 1 country.

Jared KlarquistDepartment of Immunology and Microbiology, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045; jared.klarquist@cuanschutz.edu.ORCID 0000-0002-4072-3962
Rachel CantrellDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267.ORCID 0000-0001-8424-2530
Maria A LehnDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267.ORCID 0000-0001-8400-7733
Kristin LampeDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267.
Cassandra M HenniesDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45267.
Kasper HoebeJanssen Research and Development, Johnson & Johnson, Spring House, PA 19477.
Edith M JanssenJanssen Research and Development, Johnson & Johnson, Spring House, PA 19477.
Cincinnati Children's Hospital Medical Center · USJohnson & Johnson (United States) · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Molecular Mechanisms of Immune ToleranceT32AI074491 · NIAID · NATIONAL JEWISH HEALTH · PI CAMBIER, JOHN C, PELANDA, ROBERTA · 2009 to 2023
$4.1M
Manipulating DNA Damage-response Signaling for the Treatment of Type 1 DiabetesR01DK117632 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI KATZ, JONATHAN DAVID · 2019 to 2022
$1.8M
Activating robust immunity to tumor-associated antigens:mechanisms and biologyR01CA138617 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI JANSSEN, EDITH M · 2009 to 2013
$1.5M
Dendritic Cells in the Breaking of Peripheral Tolerance in Type 1 DiabetesR01DK090978 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI JANSSEN, EDITH M, KATZ, JONATHAN DAVID · 2010 to 2012
$843k
NCI NIH HHS R01 CA138617NIAID NIH HHS T32 AI074491NIDDK NIH HHS R01 DK090978NIDDK NIH HHS R01 DK117632
6 · The paper itself

Abstract

Myriad studies have linked type I IFN to the pathogenesis of autoimmune diseases, including systemic lupus erythematosus (SLE). Although increased levels of type I IFN are found in patients with SLE, and IFN blockade ameliorates disease in many mouse models of lupus, its precise roles in driving SLE pathogenesis remain largely unknown. In this study, we dissected the effect of type I IFN sensing by CD4 T cells and B cells on the development of T follicular helper cells (T

Indexed as

AnimalsB-LymphocytesCells, CulturedDisease Models, AnimalFemaleGerminal CenterInterferon Type IKiller Cells, NaturalLupus Erythematosus, SystemicMaleMiceMice, Inbred C57BLMice, KnockoutProto-Oncogene Proteins c-bcl-6Receptor, Interferon alpha-betaT-Lymphocytes, Helper-InducerBcl6 protein, mouseIfnar1 protein, mouseInterferon Type IProto-Oncogene Proteins c-bcl-6Receptor, Interferon alpha-beta

Identifiers

PMID32161059
PMCPMC7294741
OpenAlexW3011820977

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.