Evidence map›Paper›PMID 23333205›Full record

ReviewTrends in immunology2013

The risks of targeting co-inhibitory pathways to modulate pathogen-directed T cell responses.

Helge Frebel, Annette Oxenius

Abstract readReview
In one paragraph

Review in Trends in immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Exhausted CD8Nature communications · 2020
    Article
  6. Article
  7. Article
  8. Review
  9. Programmed death-1 controls T cell survival by regulating oxidative metabolism.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  10. Review
  11. Review
  12. Article
  13. Viruses for tumor therapy.Cell host & microbe · 2014
    Review
  14. Article
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.

Helge FrebelInstitute of Microbiology, ETH Zurich, Wolfgang-Pauli-Str. 10, 8093 Zurich, Switzerland.
Annette Oxenius

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of T cell co-inhibition as a central mechanism in the regulation of adaptive immunity during infectious diseases provides new opportunities for immunotherapeutic interventions. However, the fact that T cell activity is frequently downregulated during pathogen-directed responses suggests a pivotal physiological role of co-inhibitory pathways during infectious disease. Reports of exacerbated immunopathology in conditions of impaired co-inhibition foster the view that downregulation of T cell activity is an essential negative feedback mechanism that protects from excessive pathogen-directed immunity. Thus, targeting co-inhibitory pathways can bear detrimental potential through the deregulation of physiological processes. Here, we summarize recent preclinical and clinical interventions that report immune-related adverse events after targeting co-inhibitory pathways.

Indexed as

AnimalsClinical Trials as TopicCTLA-4 AntigenDrug Evaluation, PreclinicalHumansImmunity, CellularImmunosuppressive AgentsImmunotherapyInfectionsMolecular Targeted TherapyProgrammed Cell Death 1 ReceptorReceptor Cross-TalkSuperinfectionT-LymphocytesCTLA-4 AntigenImmunosuppressive AgentsPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID23333205
PMCPMC7106470

What OpenQuestion holds

Textmetadata
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.