Evidence map›Paper›PMID 28090089›Full record

Trial reportLeukemia2017

Transfer of minimally manipulated CMV-specific T cells from stem cell or third-party donors to treat CMV infection after allo-HSCT.

M Neuenhahn, J Albrecht, M Odendahl, F Schlott, G Dössinger, M Schiemann, S Lakshmipathi, K Martin, D Bunjes, S Harsdorf and 17 more

Open access · greenAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Leukemia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 1 pooled it
16.2field-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

94 citing papers in PubMed, 1 synthesis or guideline pooled it, 159 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Adoptive T-cell therapy for virus-associated diseases.Clinical microbiology reviews · 2025
    Review
  8. Review
  9. Virus-Specific T-Cell Therapy for Prophylaxis and Treatment of Cytomegalovirus Infections After Transplantation: a Scoping Review.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  10. Virus-Specific T-Cell Therapy for the Management of Viral Infections in the Immunocompromised.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Familial CD45RAFrontiers in medicine · 2023
    Article

34 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

27 authors at 16 institutions in 1 country.

M NeuenhahnInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
J AlbrechtInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
M OdendahlInstitute for Transfusion Medicine, German Red Cross Blood Donation Service North-East, Dresden, Germany.
F SchlottInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
G DössingerInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
M SchiemannInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
S LakshmipathiInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
K MartinInstitute of Anaesthesiology, Deutsches Herzzentrum München, Klinik an der Technischen Universität München, Munich, Germany.
D BunjesDepartment of Internal Medicine III, University of Ulm, Ulm, Germany.
S HarsdorfDepartment of Internal Medicine III, University of Ulm, Ulm, Germany.
E M WeissingerDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
H MenzelDepartment of Hematology and Oncology, St Franziskus-Hospital, Flensburg, Germany.
M VerbeekDepartment of Internal Medicine III, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
L UharekMedical Clinic Hematology, Oncology and Tumorimmunology, Charité Campus Benjamin Franklin, Berlin, Germany.
N KrögerBone Marrow Transplantation Unit UKE, Hamburg, Germany.
E WagnerIII. Medical Department, Hematology, Oncology and Pneumology, University Medical Center Mainz, Mainz, Germany.
G KobbeDepartment of Hematology, Oncology and Clinical Immunology, University Hospital Duesseldorf, Medical Faculty, Heinrich Heine University Duesseldorf, Duesseldorf, Germany.
T SchroederDepartment of Hematology, Oncology and Clinical Immunology, University Hospital Duesseldorf, Medical Faculty, Heinrich Heine University Duesseldorf, Duesseldorf, Germany.
M SchmittGMP Core Facility, University of Heidelberg, Heidelberg, Germany.
G HeldInternal Medicine I, José Carreras Center for Immuno- and Gene Therapy, Saarland University Medical School, Homburg, Saar, Germany.
W HerrDepartment of Internal Medicine III, Haematology and Internal Oncology, University Hospital Regensburg, Regensburg, Germany.
L GermerothJuno Cell Therapeutics, formerly Stage Cell Therapeutics, Goettingen, Germany.
H BonigInstitute for Transfusion Medicine and Immunohematology, Johann Wolfgang Goethe University, and German Red Cross Blood Donor Service, Frankfurt, Germany.
T TonnInstitute for Transfusion Medicine, German Red Cross Blood Donation Service North-East, Dresden, Germany.
H EinseleDepartment of Internal Medicine II, University Hospital Würzburg, Wuerzburg, Germany.
D H BuschInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
G U GrigoleitDepartment of Internal Medicine II, University Hospital Würzburg, Wuerzburg, Germany.
Institute of Medical Microbiology and Hygiene · DETechnical University of Munich · DEGerman Red Cross · DEHeinrich Heine University Düsseldorf · DEUniversitätsklinikum Würzburg · DEUniversität Ulm · DEBerlin-Brandenburger Centrum für Regenerative Therapien · DECharité - Universitätsmedizin Berlin · DEDeutsches Herzzentrum München · DEHeidelberg University · DEJohannes Gutenberg University Mainz · DEMedizinische Hochschule Hannover · DESaarland University · DESt. Franziskus Hospital · DEUniversität Hamburg · DEUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytomegalovirus (CMV) infection is a common, potentially life-threatening complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT). We assessed prospectively the safety and efficacy of stem cell-donor- or third-party-donor-derived CMV-specific T cells for the treatment of persistent CMV infections after allo-HSCT in a phase I/IIa trial. Allo-HSCT patients with drug-refractory CMV infection and lacking virus-specific T cells were treated with a single dose of ex vivo major histocompatibility complex-Streptamer-isolated CMV epitope-specific donor T cells. Forty-four allo-HSCT patients receiving a T-cell-replete (D

Indexed as

AllograftsAntiviral AgentsCytomegalovirusCytomegalovirus InfectionsDrug Resistance, ViralFemaleGraft SurvivalHematologic NeoplasmsHematopoietic Stem Cell TransplantationHistocompatibilityHumansImmunocompromised HostImmunotherapy, AdoptiveLymphocyte DepletionMaleMyelodysplastic SyndromesAntiviral Agents

Identifiers

PMID28090089
OpenAlexW2573546687

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.