Evidence map›Paper›PMID 26219463›Full record

ArticleJournal of hematology & oncology2015

T cells are functionally not impaired in AML: increased PD-1 expression is only seen at time of relapse and correlates with a shift towards the memory T cell compartment.

Frauke M Schnorfeil, Felix S Lichtenegger, Katharina Emmerig, Miriam Schlueter, Julia S Neitz, Rika Draenert, Wolfgang Hiddemann, Marion Subklewe

Open access · goldAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

99 citing papers in PubMed, 145 citations in OpenAlex.

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  10. Expression of VISTA on T cells in patients with cancer colon.Journal of the Egyptian National Cancer Institute · 2025
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39 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

8 authors at 2 institutions in 1 country.

Frauke M SchnorfeilDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. frauke.schnorfeil@helmholtz-muenchen.de.
Felix S LichteneggerDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. felix.lichtenegger@med.uni-muenchen.de.
Katharina EmmerigDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. kathi_emmerig@gmx.de.
Miriam SchlueterDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. miriam-schlueter@gmx.de.
Julia S NeitzDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. julia.s.neitz@gmail.com.
Rika DraenertDivision of Clinical Infectiology, Department of Internal Medicine IV, Klinikum der Universität München, Munich, Germany. rika.draenert@med.uni-muenchen.de.
Wolfgang HiddemannDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. wolfgang.hiddemann@med.uni-muenchen.de.
Marion SubkleweDepartment of Internal Medicine III, Klinikum der Universität München, Munich, Germany. marion.subklewe@med.uni-muenchen.de.
Helmholtz Zentrum München · DELMU Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundT cell function is crucial for the success of several novel immunotherapeutic strategies for the treatment of acute myeloid leukemia (AML). However, changes in phenotype and function of T cells have been described in various hematologic malignancies, mimicking T cell exhaustion known from chronic viral infections. Detailed knowledge about phenotype and function of T cells in AML patients at different stages of the disease is indispensable for optimal development and application of immunotherapeutic strategies for this disease.

methodsWe used flow cytometry-based assays to characterize T cell phenotype and function in peripheral blood and bone marrow of AML patients at diagnosis, at relapse after intensive chemotherapy, and at relapse after allogeneic stem cell transplantation (SCT). Surface expression of CD244, PD-1, CD160, and TIM-3 was determined, and proliferation and production of IFN-γ, TNF-α, and IL-2 were measured.

resultsWe detected similar expression of inhibitory molecules on T cells from patients at diagnosis and from age-matched healthy controls. At relapse after SCT, however, PD-1 expression was significantly increased compared to diagnosis, both on CD4(+) and CD8(+) T cells. This pattern was not associated with age and cytomegalovirus (CMV) status but with a shift towards effector memory cells in relapsed AML patients. Proliferation and cytokine production assays did not reveal functional defects in T cells of AML patients, neither at diagnosis nor at relapse.

conclusionWe thus conclude that T cell exhaustion does not play a major role in AML. Immunotherapeutic strategies targeting autologous T cells thus have particularly good prospects in the setting of AML.

Indexed as

CD8-Positive T-LymphocytesFemaleHumansImmunotherapyLeukemia, Myeloid, AcuteMaleProgrammed Cell Death 1 ReceptorRecurrenceProgrammed Cell Death 1 Receptor

Identifiers

PMID26219463
PMCPMC4518596
OpenAlexW1763981524

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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.