Evidence map›Paper›PMID 21217759›Full record

ArticleNature immunology2011

Mouse CCL8, a CCR8 agonist, promotes atopic dermatitis by recruiting IL-5+ T(H)2 cells.

Sabina A Islam, Daniel S Chang, Richard A Colvin, Mike H Byrne, Michelle L McCully, Bernhard Moser, Sergio A Lira, Israel F Charo, Andrew D Luster

Abstract readComparative Study
In one paragraph

Article in Nature immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

172 citing papers in PubMed, 305 citations in OpenAlex.

  1. A phenotypically and functionally distinct human TScience translational medicine · 2017
    Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Monocyte Chemokines Enhance Atherosclerotic Plaque Necrosis After Bacterial Kidney Infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  8. Article
  9. CCR8The Journal of allergy and clinical immunology · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

112 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Sabina A IslamCenter for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Daniel S Chang
Richard A Colvin
Mike H Byrne
Michelle L McCully
Bernhard Moser
Sergio A Lira
Israel F Charo
Andrew D Luster
Harvard University · USCardiff University · GBMassachusetts General Hospital · USIcahn School of Medicine at Mount Sinai · USUniversity of California, San Francisco · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Virus discovery in cutaneous T cell lymphomaP30AR042689 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KUPPER, THOMAS S. · 1994 to 2010
$6.8M
Chemokines and Th2 Cell Trafficking in AsthmaR37AI040618 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LUSTER, ANDREW D · 2008 to 2017
$4.0M
Role of the BLTR1 receptor in lymphocyte traffickingK08AI055663 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ISLAM, SABINA A · 2003 to 2007
$601k
NIAID NIH HHS K08 AI055663NIAID NIH HHS R37 AI040618NIAMS NIH HHS P30 AR042689NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

Mouse CCL8 is a CC chemokine of the monocyte chemoattractant protein (MCP) family whose biological activity and receptor usage have remained elusive. Here we show that CCL8 is highly expressed in the skin, where it serves as an agonist for the chemokine receptor CCR8 but not for CCR2. This distinguishes CCL8 from all other MCP chemokines. CCL8 responsiveness defined a population of highly differentiated, CCR8-expressing inflammatory T helper type 2 (T(H)2) cells enriched for interleukin (IL)-5. Ccr8- and Ccl8-deficient mice had markedly less eosinophilic inflammation than wild-type or Ccr4-deficient mice in a model of chronic atopic dermatitis. Adoptive transfer studies established CCR8 as a key regulator of T(H)2 cell recruitment into allergen-inflamed skin. In humans, CCR8 expression also defined an IL-5-enriched T(H)2 cell subset. The CCL8-CCR8 chemokine axis is therefore a crucial regulator of T(H)2 cell homing that drives IL-5-mediated chronic allergic inflammation.

Indexed as

Adoptive TransferAnimalsCalcium SignalingCells, CulturedChemokine CCL1Chemokine CCL8ChemotaxisCloning, MolecularDermatitis, AtopicDisease Models, AnimalHumansInterleukin-5MiceMice, Inbred C57BLMice, KnockoutReceptors, Lymphocyte HomingCcl1 protein, mouseChemokine CCL1Chemokine CCL8Interleukin-5Receptors, Lymphocyte Homing

Identifiers

PMID21217759
PMCPMC3863381
OpenAlexW2003604887

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.