Evidence map›Paper›PMID 27105824›Full record

ReviewTrends in immunology2016

Adapting Cancer Immunotherapy Models for the Real World.

Lauryn E Klevorn, Ryan M Teague

Open access · greenAbstract readReview
In one paragraph

Review in Trends in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
5.8field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 86 citations in OpenAlex.

  1. Current trends in cancer immunotherapy: a literature-mining analysis.Cancer immunology, immunotherapy : CII · 2020
    Pooled it
  2. Pooled it
  3. Replication Study:eLife · 2018
    Pooled it
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Recent advances in the development of poly(ester amide)s-based carriers for drug delivery.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Review
  11. Engineering Heterogeneous Tumor Models for Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  12. Review
  13. Article
  14. Application of injectable hydrogels in cancer immunotherapy.Frontiers in bioengineering and biotechnology · 2023
    Review
  15. Article
  16. High throughput screening for compounds to the orphan nuclear receptor NR2F6.SLAS discovery : advancing life sciences R & D · 2022
    Article
  17. Article
  18. Translating MSC Therapy in the Age of Obesity.Frontiers in immunology · 2022
    Review
  19. Review
  20. Review
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

2 authors at 1 institution in 1 country.

Lauryn E KlevornSaint Louis University School of Medicine, Molecular Microbiology and Immunology Department, 1100 South Grand Boulevard, St Louis, MO 63104, USA.
Ryan M TeagueSaint Louis University School of Medicine, Molecular Microbiology and Immunology Department, 1100 South Grand Boulevard, St Louis, MO 63104, USA; Alvin J. Siteman NCI Comprehensive Cancer Center, St Louis, MO, USA. Electronic address: rteague@slu.edu.
Saint Louis University · US

Funding

Exploiting dual-TCR for rescue of CD8 T cell tolerance in adoptive immunotherapyR01AI087764 · NIAID · SAINT LOUIS UNIVERSITY · PI TEAGUE, RYAN M · 2010 to 2014
$1.8M
NIAID NIH HHS R01 AI087764
6 · The paper itself

Abstract

Early experiments in mice predicted the success of checkpoint blockade immunotherapy in cancer patients. However, these same animal studies failed to accurately predict many of the limitations and toxicities of treatment. One of the likely reasons for this discrepancy is the nearly universal use of young healthy mice, which stand in stark contrast to diverse patient populations varying in age, weight, diet, and hygiene. Because these variables impact immunity and metabolism, they also influence outcomes during immunotherapy and should be incorporated into the study design of preclinical experiments. Here, we discuss recent findings that highlight how efficacy and toxicity of cancer immunotherapy are affected by patient variation, and how distinct host environments can be better modeled in animal studies.

Indexed as

Age FactorsAnimalsAntibodies, MonoclonalCostimulatory and Inhibitory T-Cell ReceptorsDisease Models, AnimalDrug Evaluation, PreclinicalDrug-Related Side Effects and Adverse ReactionsHumansImmunotherapyMiceNeoplasmsTreatment OutcomeAntibodies, MonoclonalCostimulatory and Inhibitory T-Cell Receptorsagecancercheckpoint blockadeimmunotherapymicrobiotaobesity

Identifiers

PMID27105824
PMCPMC4885780
OpenAlexW2337923302

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.