Evidence map›Paper›PMID 27895644›Full record

ReviewFrontiers in immunology2016

Recent Developments in Cellular Immunotherapy for HSCT-Associated Complications.

Monica Reis, Justyna Ogonek, Marsela Qesari, Nuno M Borges, Lindsay Nicholson, Liane Preußner, Anne Mary Dickinson, Xiao-Nong Wang, Eva M Weissinger, Anne Richter

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 52 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

10 authors at 4 institutions in 2 countries.

Monica ReisHaematological Sciences, Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
Justyna OgonekTransplantation Biology, Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School , Hannover , Germany.
Marsela QesariAlcyomics Ltd. , Newcastle upon Tyne , UK.
Nuno M BorgesHaematological Sciences, Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
Lindsay NicholsonHaematological Sciences, Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
Liane PreußnerMiltenyi Biotec GmbH , Bergisch Gladbach , Germany.
Anne Mary DickinsonHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK; Alcyomics Ltd., Newcastle upon Tyne, UK.
Xiao-Nong WangHaematological Sciences, Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
Eva M WeissingerTransplantation Biology, Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School , Hannover , Germany.
Anne RichterMiltenyi Biotec GmbH , Bergisch Gladbach , Germany.
Newcastle University · GBMedizinische Hochschule Hannover · DEMiltenyi Biotec (Germany) · DEAlcyomics (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation is associated with serious complications, and improvement of the overall clinical outcome of patients with hematological malignancies is necessary. During the last decades, posttransplant donor-derived adoptive cellular immunotherapeutic strategies have been progressively developed for the treatment of graft-versus-host disease (GvHD), infectious complications, and tumor relapses. To date, the common challenge of all these cell-based approaches is their implementation for clinical application. Establishing an appropriate manufacturing process, to guarantee safe and effective therapeutics with simultaneous consideration of economic requirements is one of the most critical hurdles. In this review, we will discuss the recent scientific findings, clinical experiences, and technological advances for cell processing toward the application of mesenchymal stromal cells as a therapy for treatment of severe GvHD, virus-specific T cells for targeting life-threating infections, and of chimeric antigen receptors-engineered T cells to treat relapsed leukemia.

Indexed as

adoptive transfercell manufacturechimeric antigen receptorextracellular vesiclesimmunomodulationinfectionmesenchymal stromal cellsT cells

Identifiers

PMID27895644
PMCPMC5107577
OpenAlexW2549633191

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.