Evidence map›Paper›PMID 18804038›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2008

Combination therapy using IL-2 and anti-CD25 results in augmented natural killer cell-mediated antitumor responses.

William H D Hallett, Erik Ames, Maite Álvarez, Isabel Barao, Patricia A Taylor, Bruce R Blazar, William J Murphy

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

35 citing papers in PubMed, 45 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

William H D HallettDepartment of Microbiology and Immunology, University of Nevada School of Medicine, University of Nevada Reno, Reno, Nevada.
Erik AmesDepartment of Microbiology and Immunology, University of Nevada School of Medicine, University of Nevada Reno, Reno, Nevada.
Maite ÁlvarezDepartment of Microbiology and Immunology, University of Nevada School of Medicine, University of Nevada Reno, Reno, Nevada.
Isabel BaraoDepartment of Microbiology and Immunology, University of Nevada School of Medicine, University of Nevada Reno, Reno, Nevada.
Patricia A TaylorUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation, Minneapolis, Minnesota.
Bruce R BlazarUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation, Minneapolis, Minnesota.
William J MurphyDepartment of Microbiology and Immunology, University of Nevada School of Medicine, University of Nevada Reno, Reno, Nevada. Electronic address: wmurphy@medicine.nevada.edu.
University of Nevada, Reno · USMasonic Cancer CenterUniversity of Minnesota · US

Funding

UNDERGRADUATE RESEARCH AND TRAININGP20RR016464 · NCRR · UNIVERSITY OF NEVADA RENO · PI LORICO, AURELIO · 2001 to 2011
$30.3M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
Proteasome inhibitor (PS-341) and adoptive immunotherapyR01CA102282 · NCI · UNIVERSITY OF NEVADA RENO · PI MURPHY, WILLIAM JOSEPH · 2004 to 2013
$2.8M
Immunotherapy using NK cells to promote engraftmentR01CA093527 · NCI · UNIVERSITY OF NEVADA RENO · PI MURPHY, WILLIAM JOSEPH · 2002 to 2006
$1.3M
NCI NIH HHS R01 CA093527NCI NIH HHS R01 CA102282NCI NIH HHS R01CA102282-01A1NCI NIH HHS R01CA95327-02NCRR NIH HHS P20 RR016464NHLBI NIH HHS R01 HL056067
6 · The paper itself

Abstract

Interleukin (IL)-2 has been extensively examined to promote clinical T and natural killer (NK) cell responses. Regulatory T cells (Tregs) have been shown to regulate many aspects of the immune system, including NK cell-mediated responses. We have demonstrated that in vivo administration of IL-2 led to activation and expansion of both NK cells and immunosuppressive Tregs. Therefore, we attempted to augment NK cell antitumor effects by concurrently depleting Tregs using anti-CD25. Increased NK cell activation by IL-2 was found to be correlated with an increase in classical, short-term NK cell in vitro killing assays regardless of the depletion of Tregs. But when splenocytes of the treated mice were used in long-term tumor outgrowth experiments, we observed that prior depletion of Tregs from IL-2 administration led to improved antitumor effects compared with either treatment alone. Importantly, these in vitro data are correlated with subsequent in vivo survival of leukemia-bearing mice, in which co-treatment of IL-2 with anti-CD25 led to significantly improved survival compared with mice treated with either IL-2 alone or with Treg depletion. Prior depletion of NK1.1(+) cells, but not of CD8(+) cells, completely abrogated all antitumor effects mediated by IL-2 and anti-CD25 combination therapy. These findings demonstrate that superior NK cell-mediated antileukemic effects can be achieved with IL-2 administration and concurrent depletion of CD25(+) cells.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsCytotoxicity, ImmunologicImmunotherapyInterleukin-2Interleukin-2 Receptor alpha SubunitKiller Cells, NaturalLeukemiaLymphocyte ActivationLymphocyte DepletionMiceSurvival RateT-Lymphocytes, RegulatoryAntibodies, MonoclonalInterleukin-2Interleukin-2 Receptor alpha Subunit

Identifiers

PMID18804038
PMCPMC2735407
OpenAlexW2098548611

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.