Evidence map›Paper›PMID 37398148›Full record

ArticlebioRxiv : the preprint server for biology2023

Invasion of spontaneous germinal centers by naive B cells is rapid and persistent.

T van den Broek, K Oleinika, S Rahmayanti, C Castrillon, C E van der Poel, M C Carroll

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

T van den BroekProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston; MA 02115, USA.
K OleinikaProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston; MA 02115, USA.
S RahmayantiProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston; MA 02115, USA.
C CastrillonProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston; MA 02115, USA.
C E van der PoelProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston; MA 02115, USA.
M C CarrollProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston; MA 02115, USA.
Boston Children's Hospital · US

Funding

Evolution of autoreactive GC and epitope spreading in lupusR01AR074105 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI Michael Craig Carroll · 2018 to 2026
$4.2M
FDC regulation of self-reactive B cellsR01AI130307 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI CARROLL, MICHAEL CRAIG · 2018 to 2022
$2.7M
NIAID NIH HHS R01 AI130307NIAMS NIH HHS R01 AR074105
6 · The paper itself

Abstract

In autoreactive germinal centers (GC) initiated by a single rogue B cell clone, wild-type B cells expand and give rise to clones that target other autoantigens, known as epitope spreading. The chronic, progressive nature of epitope spreading calls for early interventions, but the kinetics and molecular requirements for wild-type B cell invasion and participation in GC remain largely unknown. With parabiosis and adoptive transfer approaches in a murine model of systemic lupus erythematosus, we demonstrate that wild-type B cells join existing GCs rapidly, clonally expand, persist, and contribute to autoantibody production and diversification. The invasion of autoreactive GCs required TLR7, B cell receptor specificity, antigen presentation, and type I interferon signaling. The adoptive transfer model provides a novel tool for identifying early events in the breaking of B cell tolerance in autoimmunity.

Identifiers

PMID37398148
PMCPMC10312503
OpenAlexW4378977452

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.