Evidence map›Paper›PMID 18060041›Full record

ArticleThe Journal of clinical investigation2008

Adoptive transfer of effector CD8+ T cells derived from central memory cells establishes persistent T cell memory in primates.

Carolina Berger, Michael C Jensen, Peter M Lansdorp, Mike Gough, Carole Elliott, Stanley R Riddell

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 522 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
522citing papers in PubMed, 1 pooled it
27.9field-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

522 citing papers in PubMed, 1 synthesis or guideline pooled it, 830 citations in OpenAlex.

  1. Pooled it
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  6. ReducingCancer immunology research · 2018
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  7. Review
  8. Nicotinamide riboside enhances adoptive T cell therapy by promoting memory differentiation and metabolic fitness.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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462 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

6 authors at 4 institutions in 2 countries.

Carolina BergerFred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA. cberger@fhcrc.org
Michael C Jensen
Peter M Lansdorp
Mike Gough
Carole Elliott
Stanley R Riddell
University of Washington · USCity Of Hope National Medical Center · USFred Hutch Cancer Center · USUniversity of British Columbia · CA

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Transplant for Lymphoma:Therapy-Related LeukemiaP50CA107399 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI FORMAN, STEPHEN J, KWAK, LARRY W · 2004 to 2022
$35.5M
ZIPRASIDONE IN NORMAL HEPATIC FUNCTION SUBJECTS &IN HEPATIC DYSFUCTIN SUBJECTSM01RR000037 · NCRR · UNIVERSITY OF WASHINGTON · PI MCDONALD, RUTH C · 1985 to 2007
$33.8M
Vaccine-Induced Immunity to CMVP01CA030206 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI FORMAN, STEPHEN J · 1985 to 2010
$31.8M
THE UW/FHCRC PROGRAM OF EXCELLENCE IN GENE THERAPYU01HL066947 · NHLBI · UNIVERSITY OF WASHINGTON · PI STAMATOYANNOPOULOS, GEORGE · 2000 to 2005
$15.7M
TARGETING ROR1 WITH CHIMERIC ANTIGEN RECEPTOR MODIFIED T CELLSR01CA114536 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Sylvain Simon · 2005 to 2026
$8.4M
CD8+ T Cell Immunity to CytomegalovirusR01AI053193 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RIDDELL, STANLEY R. · 2003 to 2013
$4.6M
NCI NIH HHS CA107399NCI NIH HHS CA18029NCI NIH HHS CA30206-25A1NCI NIH HHS P01 CA018029NCI NIH HHS P01 CA030206NCI NIH HHS P30 CA033572NCI NIH HHS P30CA33572-21NCI NIH HHS P50 CA107399NCI NIH HHS R01 CA114536NCI NIH HHS R01CA114536NCRR NIH HHS M01 RR000037NCRR NIH HHS M01RR00037NHLBI NIH HHS U01 HL066947NHLBI NIH HHS U01HL66947NIAID NIH HHS R01 AI053193NIAID NIH HHS R01AI053193
6 · The paper itself

Abstract

The adoptive transfer of antigen-specific T cells that have been expanded ex vivo is being actively pursued to treat infections and malignancy in humans. The T cell populations that are available for adoptive immunotherapy include both effector memory and central memory cells, and these differ in phenotype, function, and homing. The efficacy of adoptive immunotherapy requires that transferred T cells persist in vivo, but identifying T cells that can reproducibly survive in vivo after they have been numerically expanded by in vitro culture has proven difficult. Here we show that in macaques, antigen-specific CD8(+) T cell clones derived from central memory T cells, but not effector memory T cells, persisted long-term in vivo, reacquired phenotypic and functional properties of memory T cells, and occupied memory T cell niches. These results demonstrate that clonally derived CD8+ T cells isolated from central memory T cells are distinct from those derived from effector memory T cells and retain an intrinsic capacity that enables them to survive after adoptive transfer and revert to the memory cell pool. These results could have significant implications for the selection of T cells to expand or to engineer for adoptive immunotherapy of human infections or malignancy.

Indexed as

Adoptive TransferImmunologic MemoryAnimalsCD8-Positive T-LymphocytesCell Culture TechniquesCells, CulturedCell SurvivalMacaca nemestrinaNeoplasmsTime Factors

Identifiers

PMID18060041
PMCPMC2104476
OpenAlexW1989273697

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.