Evidence map›Paper›PMID 28841417›Full record

ArticleCell2017

Clonal Evolution of Autoreactive Germinal Centers.

Søren E Degn, Cees E van der Poel, Daniel J Firl, Burcu Ayoglu, Fahd A Al Qureshah, Goran Bajic, Luka Mesin, Claude-Agnès Reynaud, Jean-Claude Weill, Paul J Utz and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
4.7field-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

93 citing papers in PubMed, 146 citations in OpenAlex.

  1. Article
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  9. Article
  10. Dynamic control of autoreactive B cells from spontaneous germinal centers.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Article
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33 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

12 authors at 5 institutions in 4 countries.

Søren E DegnProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark. Electronic address: sdegn@biomed.au.dk.
Cees E van der PoelProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Daniel J FirlProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Burcu AyogluDepartment of Medicine, Stanford University, Stanford, CA 94305, USA.
Fahd A Al QureshahProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; King Abdulaziz City for Science and Technology, Riyadh 11442, Saudi Arabia.
Goran BajicLaboratory of Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Luka MesinWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Claude-Agnès ReynaudInstitut Necker Enfants Malades, INSERM U1151/CNRS UMS 8253, Université Paris Descartes, Sorbonne Paris Cité, 75993 Paris Cedex 14, France.
Jean-Claude WeillInstitut Necker Enfants Malades, INSERM U1151/CNRS UMS 8253, Université Paris Descartes, Sorbonne Paris Cité, 75993 Paris Cedex 14, France.
Paul J UtzDepartment of Medicine, Stanford University, Stanford, CA 94305, USA.
Gabriel D VictoraWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Michael C CarrollProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA. Electronic address: michael.carroll@childrens.harvard.edu.
Boston Children's Hospital · USDélégation Paris 5 · FRStanford University · USWhitehead Institute for Biomedical Research · USKing Abdulaziz City for Science and Technology · SA

Funding

COMPLEMENT SYSTEM AND HUMORAL IMMUNITYR01AI039246 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI CARROLL, MICHAEL CRAIG · 1996 to 2014
$6.1M
Dynamics of Antigen-Driven Selection in Germinal CentersR01AI119006 · NIAID · ROCKEFELLER UNIVERSITY · PI Gabriel D Victora · 2017 to 2026
$5.7M
BCR signaling during B cell development and maintenanceR37AI054636 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI CARROLL, MICHAEL CRAIG · 2003 to 2012
$5.7M
Giant MagnetoResistive (GMR) Sensors for Measuring Influenza VaccineR01AI125197 · NIAID · STANFORD UNIVERSITY · PI UTZ, PAUL JOSEPH, WANG, SHAN X. · 2016 to 2021
$5.0M
Ultra-Fast Epigenomic Maps for Monitoring AutoimmunityU19AI110491 · NIAID · STANFORD UNIVERSITY · PI MAECKER, HOLDEN T. · 2014 to 2018
$3.6M
FDC regulation of self-reactive B cellsR01AI130307 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI CARROLL, MICHAEL CRAIG · 2018 to 2022
$2.7M
Human complement C4 isotypes in LupusR21AI117737 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI CARROLL, MICHAEL CRAIG · 2016 to 2017
$487k
NIAID NIH HHS R01 AI039246NIAID NIH HHS R01 AI119006NIAID NIH HHS R01 AI125197NIAID NIH HHS R01 AI130307NIAID NIH HHS R21 AI117737NIAID NIH HHS R37 AI054636NIAID NIH HHS U19 AI110491
6 · The paper itself

Abstract

Germinal centers (GCs) are the primary sites of clonal B cell expansion and affinity maturation, directing the production of high-affinity antibodies. This response is a central driver of pathogenesis in autoimmune diseases, such as systemic lupus erythematosus (SLE), but the natural history of autoreactive GCs remains unclear. Here, we present a novel mouse model where the presence of a single autoreactive B cell clone drives the TLR7-dependent activation, expansion, and differentiation of other autoreactive B cells in spontaneous GCs. Once tolerance was broken for one self-antigen, autoreactive GCs generated B cells targeting other self-antigens. GCs became independent of the initial clone and evolved toward dominance of individual clonal lineages, indicating affinity maturation. This process produced serum autoantibodies to a breadth of self-antigens, leading to antibody deposition in the kidneys. Our data provide insight into the maturation of the self-reactive B cell response, contextualizing the epitope spreading observed in autoimmune disease.

Indexed as

Clonal EvolutionImmune ToleranceAnimalsAutoantibodiesAutoantigensAutoimmune DiseasesB-LymphocytesChimeraEpitopesGerminal CenterKidneyMiceMice, Inbred C57BLAutoantibodiesAutoantigensEpitopesautoantibodiesautoantigensautoimmune diseasesautoimmunityautoreactive B cellsB-lymphocytesepitope spreadinggerminal centerself-tolerancesystemic lupus erythematosus

Identifiers

PMID28841417
PMCPMC5784431
OpenAlexW2745844264

What OpenQuestion holds

Textmetadata
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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.