Evidence map›Paper›PMID 31152755›Full record

ArticleThe Journal of investigative dermatology2019

IgM Plasma Cells Reside in Healthy Skin and Accumulate with Chronic Inflammation.

R Paul Wilson, Shannon E McGettigan, Van Duc Dang, Anil Kumar, Michael P Cancro, Neda Nikbakht, William Stohl, Gudrun F Debes

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Interplay between Humoral and CLAInternational journal of molecular sciences · 2021
    Trial
  3. Germinal center responses at barrier organ sites.Current opinion in immunology · 2026
    Review
  4. Review
  5. Hidden immune memory niches in inflammatory skin diseases.bioRxiv : the preprint server for biology · 2026
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. B cells in non-lymphoid tissues.Nature reviews. Immunology · 2025
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. TNF-α Limits Serological Memory by Disrupting the Bone Marrow Niche.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

R Paul WilsonDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Shannon E McGettiganDepartment of Microbiology and Immunology, Sidney Kimmel Medical College and Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Van Duc DangDepartment of Microbiology and Immunology, Sidney Kimmel Medical College and Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA; Department of Cell Biology, Faculty of Biology, VNU University of Science, Hanoi, Vietnam; Vinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Anil KumarDepartment of Microbiology and Immunology, Sidney Kimmel Medical College and Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Michael P CancroDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Neda NikbakhtDepartment of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
William StohlDivision of Rheumatology, University of Southern California Keck School of Medicine, Los Angeles, California, USA.
Gudrun F DebesDepartment of Microbiology and Immunology, Sidney Kimmel Medical College and Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address: Gudrun.debes@jefferson.edu.
Sidney Kimmel Cancer Center · USThomas Jefferson University · USUniversity of Pennsylvania · USUniversity of Southern California · USVinmec International Hospital · VN

Funding

Study Design and Data AnalysisP30AR069589 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice · 2016 to 2026
$8.6M
Migration and function of skin B cellsR01AR067751 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI DEBES, GUDRUN PHILOMENA · 2016 to 2020
$1.7M
Migration and function of cutaneous B cellsR01AI127389 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI DEBES, GUDRUN PHILOMENA · 2017 to 2021
$1.6M
Training grant on Vaccines and Immunotherapies for Infectious Diseases and CancerT32AI134646 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SCHNELL, MATTHIAS JOHANNES, SIGAL, LUIS J · 2018 to 2022
$1.1M
NIAID NIH HHS R01 AI127389NIAID NIH HHS T32 AI134646NIAMS NIH HHS P30 AR069589NIAMS NIH HHS R01 AR067751
6 · The paper itself

Abstract

Antibodies are key to cutaneous host defense and inflammation. Despite their importance, the mechanisms by which skin antibodies are sustained are poorly described. Here, we identified that, in addition to antibody production in lymphoid tissues, plasma cells reside in healthy mouse and human skin. In naïve mice, IgM was the predominant isotype produced in skin. Skin plasma cells developed independently of T cells and microbiota. Importantly, chronic skin inflammation promoted the massive accumulation of IgM-secreting cells, and cutaneous immunization directed both T cell-dependent and -independent antigen-specific IgM-secreting cells into skin. Unlike their counterparts in lymphoid tissues, cutaneous IgM-secreting cells were completely dependent on survival factors such as a proliferation-inducing ligand or B cell-activating factor, which were constitutively expressed and upregulated during inflammation in skin. Our data support a model in which skin plasma cells supply natural and adaptive IgM to the cutaneous environment, thereby supporting homeostatic skin barrier functions and providing defense against pathogen intrusion. Our results are also of potential relevance for manipulation of cutaneous plasma cells in inflammatory skin diseases or cutaneous plasma cell malignancies.

Indexed as

Immunity, CellularAnimalsAntibody FormationB-LymphocytesChronic DiseaseDisease Models, AnimalFemaleHumansImmunoglobulin MInflammationLymphocyte ActivationMaleMicePlasma CellsReference ValuesSkinImmunoglobulin M

Identifiers

PMID31152755
PMCPMC6874734
OpenAlexW2947698879

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.