Evidence map›Paper›PMID 29967180›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Identification of a new subset of lymph node stromal cells involved in regulating plasma cell homeostasis.

Hsin-Ying Huang, Ana Rivas-Caicedo, François Renevey, Hélène Cannelle, Elisa Peranzoni, Leonardo Scarpellino, Debbie L Hardie, Arnaud Pommier, Karin Schaeuble, Stéphanie Favre and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 112 citations in OpenAlex.

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  16. Lymphoid stroma in all its states.Frontiers in immunology · 2025
    Review
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  18. Unique and redundant roles of mouse BCMA, TACI, BAFF, APRIL, and IL-6 in supporting antibody-producing cells in different tissues.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  19. Review
  20. Protective fibroblastic niches in secondary lymphoid organs.The Journal of experimental medicine · 2024
    Review

12 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

16 authors at 7 institutions in 3 countries.

Hsin-Ying HuangDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Ana Rivas-CaicedoINSERM, U1016, Institut Cochin, 75014 Paris, France.
François ReneveyDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Hélène CannelleDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Elisa PeranzoniINSERM, U1016, Institut Cochin, 75014 Paris, France.
Leonardo ScarpellinoDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Debbie L HardieCentre for Translational Inflammation Research, School of Immunity and Infection, University of Birmingham, Queen Elizabeth Hospital, Birmingham B15 2WD, United Kingdom.
Arnaud PommierINSERM, U1016, Institut Cochin, 75014 Paris, France.
Karin SchaeubleDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Stéphanie FavreDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Tobias K VogtDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Fernando Arenzana-SeisdedosUnité de Pathogénie Virale, Département de Virologie, INSERM U819, Institut Pasteur, 75015 Paris, France.
Pascal SchneiderDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland.
Christopher D BuckleyCentre for Translational Inflammation Research, School of Immunity and Infection, University of Birmingham, Queen Elizabeth Hospital, Birmingham B15 2WD, United Kingdom.
Emmanuel DonnadieuINSERM, U1016, Institut Cochin, 75014 Paris, France.
Sanjiv A LutherDepartment of Biochemistry, Center for Immunity and Infection, University of Lausanne, 1066 Epalinges, Switzerland; Sanjiv.Luther@unil.ch.
University of Lausanne · CHInserm · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRInstitut Cochin · FRQueen Elizabeth Hospital Birmingham · GBUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-secreting plasma cells (PCs) arise rapidly during adaptive immunity to control infections. The early PCs are retained within the reactive lymphoid organ where their localization and homeostasis rely on extrinsic factors, presumably produced by local niche cells. While myeloid cells have been proposed to form those niches, the contribution by colocalizing stromal cells has remained unclear. Here, we characterized a subset of fibroblastic reticular cells (FRCs) that forms a dense meshwork throughout medullary cords of lymph nodes (LNs) where PCs reside. This medullary FRC type is shown to be anatomically, phenotypically, and functionally distinct from T zone FRCs, both in mice and humans. By using static and dynamic imaging approaches, we provide evidence that medullary FRCs are the main cell type in contact with PCs guiding them in their migration. Medullary FRCs also represent a major local source of the PC survival factors IL-6, BAFF, and CXCL12, besides also producing APRIL. In vitro, medullary FRCs alone or in combination with macrophages promote PC survival while other LN cell types do not have this property. Thus, we propose that this FRC subset, together with medullary macrophages, forms PC survival niches within the LN medulla, and thereby helps in promoting the rapid development of humoral immunity, which is critical in limiting early pathogen spread.

Indexed as

Antibody FormationAnimalsB-Cell Activating FactorChemokine CXCL12HomeostasisInterleukin-6Lymph NodesMaleMicePlasma CellsStromal CellsB-Cell Activating FactorChemokine CXCL12Cxcl12 protein, mouseInterleukin-6interleukin-6, mouseTnfsf13b protein, mouseextrafollicular B cell differentiationFRC subsetshumoral responselymph node medullaplasma cell survival

Identifiers

PMID29967180
PMCPMC6055158
OpenAlexW2810248805

What OpenQuestion holds

Textmetadata
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.