Evidence map›Paper›PMID 23017138›Full record

ReviewImmunological investigations2012

Metabolism of L-arginine by myeloid-derived suppressor cells in cancer: mechanisms of T cell suppression and therapeutic perspectives.

Patrick Raber, Augusto C Ochoa, Paulo C Rodríguez

Open access · greenAbstract readReview
In one paragraph

Review in Immunological investigations, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 179 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
179citing papers in PubMed, 1 pooled it
8.7field-weighted citation impact, top 2% 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

179 citing papers in PubMed, 1 synthesis or guideline pooled it, 298 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Myeloid-derived suppressor cells in sepsis: drivers of persistent immunosuppression and targets for precision immunotherapy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Myeloid-derived suppressor cells modulation in the context of tumor microenvironment for gastric cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

119 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

3 authors at 1 institution in 1 country.

Patrick RaberDepartment of Microbiology, Immunology and Parasitology, Louisiana State University Health Sciences Center, NewOrleans, Louisiana, USA. praber@lsuhsc.edu
Augusto C Ochoa
Paulo C Rodríguez
Louisiana State University Health Sciences Center New Orleans · US

Funding

Mentoring Translational Researchers in LouisianaP20GM103501 · NIGMS · LSU HEALTH SCIENCES CENTER · PI OCHOA, AUGUSTO C. · 2012 to 2014
$6.3M
Arginase Production in Cancer: Evading Immune ResponseR01CA107974 · NCI · LSU HEALTH SCIENCES CENTER · PI OCHOA, AUGUSTO C. · 2004 to 2015
$3.6M
INDUCTION OF ANERGY AND ALTERED SIGNAL TRANSDUCTIONR01CA082689 · NCI · LSU HEALTH SCIENCES CENTER · PI OCHOA, AUGUSTO C. · 1999 to 2013
$3.1M
Notch-1 in T Cells: a central mediator of tumor induced anergyR21CA162133 · NCI · LSU HEALTH SCIENCES CENTER · PI RODRIGUEZ, PAULO CESAR · 2012 to 2013
$330k
NCI NIH HHS R01 CA082689NCI NIH HHS R01 CA107974NCI NIH HHS R21 CA162133NIGMS NIH HHS P20 GM103501
6 · The paper itself

Abstract

Patients with cancer have an impaired T cell response that can decrease the potential therapeutic benefit of cancer vaccines and other forms of immunotherapy. The establishment of a chronic inflammatory environment in patients with cancer plays a critical role in the induction of T cell dysfunction. The accumulation of myeloid-derived suppressor cells (MDSC) in tumor bearing hosts is a hallmark of malignancy-associated inflammation and a major mediator of the induction of T cell suppression in cancer. Recent findings in tumor bearing mice and cancer patients indicate that the increased metabolism of L-Arginine (L-Arg) by MDSC producing Arginase I inhibits T cell lymphocyte responses. Here, we discuss some of the most recent concepts of how MDSC expressing Arginase I may regulate T cell function in cancer and suggest possible therapeutic interventions to overcome this inhibitory effect.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsArginaseArginineCytokinesHumansImmune ToleranceInflammationMiceMyeloid Progenitor CellsNeoplasm ProteinsNeoplasmsSignal TransductionT-LymphocytesARG1 protein, humanArginaseArginineCytokinesNeoplasm Proteins

Identifiers

PMID23017138
PMCPMC3519282
OpenAlexW2060727628

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.