Evidence map›Paper›PMID 35670812›Full record

ArticleThe Journal of experimental medicine2022

CXCR4+ Treg cells control serum IgM levels and natural IgM autoantibody production by B-1 cells in the bone marrow.

Shlomo Elias, Rahul Sharma, Michael Schizas, Izabella Valdez, Sham Rampersaud, Sun-Mi Park, Paula Gonzalez-Figueroa, Quan-Zhen Li, Beatrice Hoyos, Alexander Y Rudensky

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Blocking CXCR4Genome medicine · 2025
    Article
  5. IL-2Rα is dispensable for murine B cell development and humoral response.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
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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 at 3 institutions in 2 countries.

Shlomo EliasImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-5055-5317
Rahul SharmaImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-8805-9431
Michael SchizasImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-9285-6951
Izabella ValdezImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-8652-7043
Sham RampersaudImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-7473-4144
Sun-Mi ParkMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-2370-0432
Paula Gonzalez-FigueroaDepartment of Immunology and Infectious Disease, The John Curtin School of Medical Research, The Australian National University, Canberra, Australia.ORCID 0000-0001-8270-552X
Quan-Zhen LiMicroarray and Immune Phenotyping Core Facility, Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-7257-0489
Beatrice HoyosImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-3689-2445
Alexander Y RudenskyImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1280-2898
Memorial Sloan Kettering Cancer Center · USAustralian National University · AUThe University of Texas Southwestern Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
SELF PEPTIDES BOUND TO MHC CLASS II IN T CELL SELECTIONR01AI034206 · NIAID · UNIVERSITY OF WASHINGTON · PI Alexander Y Rudensky · 1998 to 2026
$6.4M
Cancer Research InstituteNCI NIH HHS P30 CA008748NIAID NIH HHS R01 AI034206
6 · The paper itself

Abstract

Regulatory T (Treg) cells represent a specialized lineage of suppressive CD4+ T cells whose functionality is critically dependent on their ability to migrate to and dwell in the proximity of cells they control. Here we show that continuous expression of the chemokine receptor CXCR4 in Treg cells is required for their ability to accumulate in the bone marrow (BM). Induced CXCR4 ablation in Treg cells led to their rapid depletion and consequent increase in mature B cells, foremost the B-1 subset, observed exclusively in the BM without detectable changes in plasma cells or hematopoietic stem cells or any signs of systemic or local immune activation elsewhere. Dysregulation of BM B-1 B cells was associated with a highly specific increase in IgM autoantibodies and total serum IgM levels. Thus, Treg cells control autoreactive B-1 B cells in a CXCR4-dependent manner. These findings have significant implications for understanding the regulation of B cell autoreactivity and malignancies.

Indexed as

B-Lymphocyte SubsetsT-Lymphocytes, RegulatoryBone MarrowBone Marrow CellsImmunoglobulin MReceptors, CXCR4Immunoglobulin MReceptors, CXCR4

Identifiers

PMID35670812
PMCPMC9178519
OpenAlexW4281661425

What OpenQuestion 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 OpenQuestion graph.