Evidence map›Paper›PMID 19859065›Full record

ReviewNature reviews. Immunology2009

Engineering lymphocyte subsets: tools, trials and tribulations.

Carl H June, Bruce R Blazar, James L Riley

Abstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing 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

107 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. CAR-T cell therapy for cancer: current challenges and future directions.Signal transduction and targeted therapy · 2025
    Review
  5. Article
  6. Article
  7. CircRNA Regulation of T Cells in Cancer: Unraveling Potential Targets.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

47 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.

Carl H JuneDepartment of Pathology and Laboratory Medicine and Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA. cjune@exchange.upenn.edu
Bruce R Blazar
James L Riley

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
VECTOR DEVELOPMENT /PRECLINICAL TESTINGP01CA066726 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KALOS, MICHAEL D · 1995 to 2016
$18.2M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI CUTLER, COREY S · 2009 to 2019
$17.5M
Targeting the PD-1 signaling pathway to rescue HIV T cell dysfunctionP01AI080192 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI · 2008 to 2012
$12.6M
Sequencing and Viral Evolution CoreU19AI082628 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI RILEY, JAMES L. · 2009 to 2013
$8.9M
Lentivirus-based Immunogene Therapy for HIV InfectionU19AI066290 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI JUNE, CARL H. · 2005 to 2009
$7.2M
IN VIVO PREVENTION OF MURINE GVHDR01AI034495 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1993 to 2016
$6.2M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
GVL TO REDUCE AML RELAPSE AFTER MURINE ALLOGENEIC BMTR01CA072669 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1997 to 2017
$4.9M
IMMUNOTHERAPY WITH CAR T CELLSR01CA120409 · NCI · UNIVERSITY OF PENNSYLVANIA · PI JUNE, CARL H., ZHAO, YANGBING · 2006 to 2016
$2.7M
NCI NIH HHS 1R01 CA 120409NCI NIH HHS 5P01 CA 066726NCI NIH HHS 5R01 CA 105216NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA066726NCI NIH HHS P01 CA 142106NCI NIH HHS P01 CA142106NCI NIH HHS R01 CA072669NCI NIH HHS R01 CA105216NCI NIH HHS R01 CA 113783NCI NIH HHS R01 CA113783NCI NIH HHS R01 CA120409NCI NIH HHS R01 CA 72669NCI NIH HHS R41 CA 130547NCI NIH HHS R41 CA130547NHLBI NIH HHS 2R01 HL 56067NHLBI NIH HHS R01 HL056067NIAID NIH HHS 1U19 AI 082628NIAID NIH HHS P01 AI 056299NIAID NIH HHS P01 AI056299NIAID NIH HHS P01 AI 080192NIAID NIH HHS P01 AI080192NIAID NIH HHS P30 AI 045008NIAID NIH HHS P30 AI045008NIAID NIH HHS R01 AI034495NIAID NIH HHS R01 AI 057838NIAID NIH HHS R01 AI057838NIAID NIH HHS R01 AI 34495NIAID NIH HHS U19 AI 066290NIAID NIH HHS U19 AI066290NIAID NIH HHS U19 AI 082628NIAID NIH HHS U19 AI082628
6 · The paper itself

Abstract

Cell-based therapies with various lymphocyte subsets hold promise for the treatment of several diseases, including cancer and disease resulting from inflammation and infection. The ability to genetically engineer lymphocyte subsets has the potential to improve the natural immune response and correct impaired immunity. In this Review we focus on the lymphocyte subsets that have been modified genetically or by other means for therapeutic benefit, on the technologies used to engineer lymphocytes and on the latest progress and hurdles in translating these technologies to the clinic.

Indexed as

Adoptive TransferGenetic EngineeringAnimalsClinical Trials as TopicEpigenesis, GeneticGenetic VectorsHumansLymphocyte SubsetsTransduction, GeneticTransgenes

Identifiers

PMID19859065
PMCPMC3412112

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.