Evidence map›Paper›PMID 31377844›Full record

ReviewCellular and molecular life sciences : CMLS2019

Dual CCR5/CCR2 targeting: opportunities for the cure of complex disorders.

Laura Fantuzzi, Maria Tagliamonte, Maria Cristina Gauzzi, Lucia Lopalco

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
8.4field-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

74 citing papers in PubMed, 148 citations in OpenAlex.

  1. Article
  2. Article
  3. GPCR Heterodimers: Implications for Biased Signaling.Handbook of experimental pharmacology · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Engineered immunological niche directs therapeutic development in models of progressive multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Innate Immunity and Synovitis: Key Players in Osteoarthritis Progression.International journal of molecular sciences · 2024
    Review
  14. Updates in Immunotherapy for Pancreatic Cancer.Journal of clinical medicine · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

14 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 3 institutions in 1 country.

Laura FantuzziNational Center for Global Health, Istituto Superiore di Sanità, Rome, Italy. laura.fantuzzi@iss.it.ORCID http://orcid.org/0000-0002-0869-2596
Maria TagliamonteCancer Immunoregulation Unit, Istituto Nazionale Tumori- IRCCS-"Fond G. Pascale", Naples, Italy.ORCID http://orcid.org/0000-0002-7167-4817
Maria Cristina GauzziNational Center for Global Health, Istituto Superiore di Sanità, Rome, Italy.ORCID http://orcid.org/0000-0002-2996-5231
Lucia LopalcoImmunobiology of HIV Unit, Division Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy. lopalco.lucia@hsr.it.ORCID http://orcid.org/0000-0003-3812-1759
Istituto Superiore di Sanità · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITVita-Salute San Raffaele University · IT

Funding

Ministero della Salute RF-2011-02347224
6 · The paper itself

Abstract

The chemokine system mediates acute inflammation by driving leukocyte migration to damaged or infected tissues. However, elevated expression of chemokines and their receptors can contribute to chronic inflammation and malignancy. Thus, great effort has been taken to target these molecules. The first hint of the druggability of the chemokine system was derived from the role of chemokine receptors in HIV infection. CCR5 and CXCR4 function as essential co-receptors for HIV entry, with the former accounting for most new HIV infections worldwide. Not by chance, an anti-CCR5 compound, maraviroc, was the first FDA-approved chemokine receptor-targeting drug. CCR5, by directing leukocytes to sites of inflammation and regulating their activation, also represents an important player in the inflammatory response. This function is shared with CCR2 and its selective ligand CCL2, which constitute the primary chemokine axis driving the recruitment of monocytes/macrophages to inflammatory sites. Both receptors are indeed involved in the pathogenesis of several immune-mediated diseases, and dual CCR5/CCR2 targeting is emerging as a more efficacious strategy than targeting either receptor alone in the treatment of complex human disorders. In this review, we focus on the distinctive and complementary contributions of CCR5 and CCR2/CCL2 in HIV infection, multiple sclerosis, liver fibrosis and associated hepatocellular carcinoma. The emerging therapeutic approaches based on the inhibition of these chemokine axes are highlighted.

Indexed as

Carcinoma, HepatocellularChemokine CCL2Gene TargetingHIVHIV InfectionsHumansInflammationLiver CirrhosisLiver NeoplasmsMultiple SclerosisReceptors, CCR2Receptors, CCR5CCL2 protein, humanCCR2 protein, humanCCR5 protein, humanChemokine CCL2Receptors, CCR2Receptors, CCR5AIDSAutoimmunityChemokine receptor antagonistLiver diseaseNeuroinflammationTherapeutic antibody

Identifiers

PMID31377844
PMCPMC6892368
OpenAlexW2966771790

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.