Evidence map›Paper›PMID 18684977›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

CD28 costimulation is essential for human T regulatory expansion and function.

Tatiana N Golovina, Tatiana Mikheeva, Megan M Suhoski, Nicole A Aqui, Victoria C Tai, Xiaochuan Shan, Ronghua Liu, R Robert Balcarcel, Nancy Fisher, Bruce L Levine and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
6.9field-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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 165 citations in OpenAlex.

  1. Pooled it
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  20. HIV-1-Infected CD4Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article

36 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

15 authors at 4 institutions in 1 country.

Tatiana N GolovinaDepartment of Pathology and Laboratory Medicine and Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.
Tatiana Mikheeva
Megan M Suhoski
Nicole A Aqui
Victoria C Tai
Xiaochuan Shan
Ronghua Liu
R Robert Balcarcel
Nancy Fisher
Bruce L Levine
Richard G Carroll
Noel Warner
Bruce R Blazar
Carl H June
James L Riley
Cancer Research Institute · USBD Biosciences (United States) · USBD Technologie (United States) · USUniversity of Minnesota · US

Funding

T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
T CELL TARGETING FOR GVHDR37HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R. · 1998 to 2007
$3.2M
TRANSFUSION MEDICINE RESEARCH TRAINING PROGRAMT32HL007775 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SIEGEL, DONALD LAWRENCE · 1993 to 2023
$2.8M
Regulation of human T cell activation by the CD28 familyR01AI057838 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI RILEY, JAMES L. · 2004 to 2008
$1.7M
Culture systems to propogate human T cell subsetsR01CA105216 · NCI · UNIVERSITY OF PENNSYLVANIA · PI JUNE, CARL H. · 2004 to 2008
$1.5M
Development of tumor based antigen presenting cellsR01CA113783 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RILEY, JAMES L. · 2005 to 2008
$1.1M
NCI NIH HHS P01CA670493NCI NIH HHS R01 CA105216NCI NIH HHS R01CA105216NCI NIH HHS R01 CA113783NHLBI NIH HHS R01 HL056067NHLBI NIH HHS R37 HL056067NHLBI NIH HHS R37HL56067NHLBI NIH HHS T32 HL007775NIAID NIH HHS R01 AI057838NIAID NIH HHS R01AI057838
6 · The paper itself

Abstract

The costimulatory requirements required for peripheral blood T regulatory cells (Tregs) are unclear. Using cell-based artificial APCs we found that CD28 but not ICOS, OX40, 4-1BB, CD27, or CD40 ligand costimulation maintained high levels of Foxp3 expression and in vitro suppressive function. Only CD28 costimulation in the presence of rapamycin consistently generated Tregs that consistently suppressed xenogeneic graft-vs-host disease in immunodeficient mice. Restimulation of Tregs after 8-12 days of culture with CD28 costimulation in the presence of rapamycin resulted in >1000-fold expansion of Tregs in <3 wk. Next, we determined whether other costimulatory pathways could augment the replicative potential of CD28-costimulated Tregs. We observed that while OX40 costimulation augmented the proliferative capacity of CD28-costimulated Tregs, Foxp3 expression and suppressive function were diminished. These studies indicate that the costimulatory requirements for expanding Tregs differ from those for T effector cells and, furthermore, they extend findings from mouse Tregs to demonstrate that human postthymic Tregs require CD28 costimulation to expand and maintain potent suppressive function in vivo.

Indexed as

Adoptive TransferAnimalsCD28 AntigensCell Culture TechniquesFemaleGraft vs Host DiseaseHumansK562 CellsLymphocyte ActivationMaleMiceMice, Inbred NODMice, SCIDSignal TransductionThymus GlandT-Lymphocytes, RegulatoryCD28 Antigens

Identifiers

PMID18684977
PMCPMC2556987
OpenAlexW2106024349

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.