Evidence map›Paper›PMID 18303997›Full record

ReviewAnnual review of immunology2008

Monocyte-mediated defense against microbial pathogens.

Natalya V Serbina, Ting Jia, Tobias M Hohl, Eric G Pamer

Registry-linked trialAbstract readReview
In one paragraph

Review in Annual review of immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05025787 (EN20-01), which is not on this map. Cited by 614 papers.

0numbers the graph read from it
0cells of the map it votes in
614citing papers in PubMed
28.2field-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.

NCT05025787 phase2completednot on this mapstarted 2021, after this paper: background citation

EN20-01: A 24 Week Study to Evaluate the Safety and Efficacy of CNTX-6970 in Subjects With Moderate to Severe Knee Osteoarthritis Pain.

TypeinterventionalSponsorMaurizio Fava, MDRan2021 to 2024Enrolled55ConditionsKnee OsteoarthritisArmsCNTX-6970, Placebo
3 · Its place in the literature

Who cites it

614 citing papers in PubMed, 1,107 citations in OpenAlex.

  1. Trial
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  9. Article
  10. Review
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  12. AMetabolites · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. ATG5 Plays a Role inTransboundary and emerging diseases · 2026
    Article
  18. Article
  19. Review
  20. Article

554 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

4 authors at 1 institution in 1 country.

Natalya V SerbinaInfectious Diseases Service, Department of Medicine, Immunology Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA. serbinan@mskcc.org
Ting Jia
Tobias M Hohl
Eric G Pamer
Memorial Sloan Kettering Cancer Center · US

Funding

CC-chemokines in Listeria infection.R37AI039031 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI PAMER, ERIC G. · 2007 to 2016
$4.5M
MSKCC Clinical Oncology Research Career Development ProgramK12CA120121 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SCHWARTZ, GARY K · 2006 to 2010
$3.0M
CD4 T Cell Responses to M. Tuberculosis InfectionR01AI080619 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI GLICKMAN, MICHAEL S, PAMER, ERIC G. · 2009 to 2013
$2.3M
Inflammation and T cell immunity to ListeriaR01AI039031 · NIAID · YALE UNIVERSITY · PI PAMER, ERIC G · 1996 to 2006
$1.9M
Research Training in Infectious DiseasesT32AI055409 · NIAID · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PAMER, ERIC G. · 2004 to 2008
$1.1M
NCI NIH HHS K12 CA120121NIAID NIH HHS AI39031NIAID NIH HHS R01 AI039031NIAID NIH HHS R01 AI080619NIAID NIH HHS R37 AI039031NIAID NIH HHS T32 AI055409
6 · The paper itself

Abstract

Circulating blood monocytes supply peripheral tissues with macrophage and dendritic cell (DC) precursors and, in the setting of infection, also contribute directly to immune defense against microbial pathogens. In humans and mice, monocytes are divided into two major subsets that either specifically traffic into inflamed tissues or, in the absence of overt inflammation, constitutively maintain tissue macrophage/DC populations. Inflammatory monocytes respond rapidly to microbial stimuli by secreting cytokines and antimicrobial factors, express the CCR2 chemokine receptor, and traffic to sites of microbial infection in response to monocyte chemoattractant protein (MCP)-1 (CCL2) secretion. In murine models, CCR2-mediated monocyte recruitment is essential for defense against Listeria monocytogenes, Mycobacterium tuberculosis, Toxoplasma gondii, and Cryptococcus neoformans infection, implicating inflammatory monocytes in defense against bacterial, protozoal, and fungal pathogens. Recent studies indicate that inflammatory monocyte recruitment to sites of infection is complex, involving CCR2-mediated emigration of monocytes from the bone marrow into the bloodstream, followed by trafficking into infected tissues. The in vivo mechanisms that promote chemokine secretion, monocyte differentiation and trafficking, and finally monocyte-mediated microbial killing remain active and important areas of investigation.

Indexed as

AnimalsCell DifferentiationChemotaxisHumansImmunity, CellularImmunity, MucosalInfectionsMonocyte Chemoattractant ProteinsMonocytesReceptors, CCR2Monocyte Chemoattractant ProteinsReceptors, CCR2

Identifiers

PMID18303997
PMCPMC2921669
OpenAlexW2109357160

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.