Evidence map›Paper›PMID 40210692›Full record

ArticleCellular & molecular immunology2025

Activation and maturation of antigen-specific B cells in nonectopic lung infiltrates are independent of germinal center reactions in the draining lymph node.

Sarah-Sophie Schacht, Josefine Graffunder, Pawel Durek, Jonas Wehrenberg, Annette Siracusa, Charlotte Biese, Mir-Farzin Mashreghi, Kevin Thurley, Laura Bauer, Andreas Hutloff

Abstract read
In one paragraph

Article in Cellular & molecular immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Germinal center responses at barrier organ sites.Current opinion in immunology · 2026
    Review
  4. Review
  5. Article
  6. 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

10 authors.

Sarah-Sophie SchachtInstitute of Immunology, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID 0000-0003-2512-1741
Josefine GraffunderChronic Immune Reactions, German Rheumatism Research Centre, A Leibniz Institute, Berlin, Germany.
Pawel DurekTherapeutic Gene Regulation, German Rheumatism Research Centre, A Leibniz Institute, Berlin, Germany.ORCID 0000-0002-6179-0670
Jonas WehrenbergInstitute of Immunology, University Hospital Schleswig-Holstein, Kiel, Germany.
Annette SiracusaChronic Immune Reactions, German Rheumatism Research Centre, A Leibniz Institute, Berlin, Germany.
Charlotte BieseInstitute of Immunology, University Hospital Schleswig-Holstein, Kiel, Germany.
Mir-Farzin MashreghiTherapeutic Gene Regulation, German Rheumatism Research Centre, A Leibniz Institute, Berlin, Germany.ORCID 0000-0002-8015-6907
Kevin ThurleyInstitute for Experimental Oncology, Biomathematics Division, University Hospital Bonn, Bonn, Germany.
Laura BauerInstitute of Immunology, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID 0000-0002-1435-8121
Andreas HutloffInstitute of Immunology, University Hospital Schleswig-Holstein, Kiel, Germany. andreas.hutloff@uksh.de.ORCID 0000-0002-0572-8151

Funding

Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01GL2401C, CONAN, TreATDeutsche Forschungsgemeinschaft (German Research Foundation) EXC2151, EXC2047Deutsche Forschungsgemeinschaft (German Research Foundation) HU 1294/8-1, HU 1294/8-2, SFB 1526-A08Leibniz-Gemeinschaft (Leibniz Association) TargArt, ImpACt
6 · The paper itself

Abstract

Pulmonary T and B cells are important for protection of this mucosal barrier site. While viral infections lead to the development of ectopic lymphoid structures highly similar to those in germinal centers in secondary lymphoid organs, little is known about how T/B cooperation occurs in the unstructured, diffuse tissue infiltrates characteristic of autoimmune diseases and nonviral infections. Using a mouse model of interstitial lung inflammation, we found that naive B cells are directly activated in lung tissue. Despite the absence of any germinal center-like structures, the interaction of B cells with peripheral T helper cells results in efficient somatic hypermutation and class switching. As antigen-presenting cells, macrophages are critical for this process. Unique B-cell repertoires indicated that the lung response was autonomous from the lung-draining lymph node. Only lung GC-like B cells were switched to IgA and had a broader repertoire, making them ideal candidates for producing broadly neutralizing immunoglobulins against respiratory pathogens.

Indexed as

B-LymphocytesGerminal CenterLungLymph NodesLymphocyte ActivationAnimalsImmunoglobulin AImmunoglobulin Class SwitchingMiceMice, Inbred C57BLT-Lymphocytes, Helper-InducerImmunoglobulin Agerminal centerimmunoglobulin ALung inflammationmacrophagesperipheral T helper cellssomatic hypermutation

Identifiers

PMID40210692
PMCPMC12125278

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.