Evidence map›Paper›PMID 23152545›Full record

ArticleBlood2013

Immunotherapeutic strategies to prevent and treat human herpesvirus 6 reactivation after allogeneic stem cell transplantation.

Ulrike Gerdemann, Laura Keukens, Jacqueline M Keirnan, Usha L Katari, Chinh T Q Nguyen, Anne P de Pagter, Carlos A Ramos, Alana Kennedy-Nasser, Stephen M Gottschalk, Helen E Heslop and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Observational
  6. Review
  7. The generation and application of antigen-specific T cell therapies for cancer and viral-associated disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  8. Modified T cells as therapeutic agents.Hematology. American Society of Hematology. Education Program · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Herpesviral Latency-Common Themes.Pathogens (Basel, Switzerland) · 2020
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Identification of CD4 and H-2KScientific reports · 2019
    Article
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

13 authors at 5 institutions in 2 countries.

Ulrike GerdemannCenter for Cell and Gene Therapy, Baylor College of Medicine, Methodist Hospital, Texas Children's Hospital, Houston, TX 77030, USA.
Laura Keukens
Jacqueline M Keirnan
Usha L Katari
Chinh T Q Nguyen
Anne P de Pagter
Carlos A Ramos
Alana Kennedy-Nasser
Stephen M Gottschalk
Helen E Heslop
Malcolm K Brenner
Cliona M Rooney
Ann M Leen
Methodist Hospital · USHouston Methodist · USTexas Children's Hospital · USUniversity Medical Center Utrecht · NLUtrecht University · NL

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
NCI NIH HHS P30 CA125123
6 · The paper itself

Abstract

Human herpesvirus (HHV) 6 causes substantial morbidity and mortality in the immunocompromised host and has no approved therapy. Adoptive transfer of virus specific T cells has proven safe and apparently effective as prophylaxis and treatment of other virus infections in immunocompromised patients; however, extension to subjects with HHV6 has been hindered by the paucity of information on targets of cellular immunity. We now characterize the cellular immune response from 20 donors against 5 major HHV6B antigens predicted to be immunogenic and define a hierarchy of immunodominance of antigens based on the frequency of responding donors and the magnitude of the T-cell response. We identified specific epitopes within these antigens and expanded the HHV6 reactive T cells using a GMP-compliant protocol. The expanded population comprised both CD4(+) and CD8(+) T cells that were able to produce multiple effector cytokines and kill both peptide-loaded and HHV6B wild-type virus-infected target cells. Thus, we conclude that adoptive T-cell immunotherapy for HHV6 is a practical objective and that the peptide and epitope tools we describe will allow such cells to be prepared, administered, and monitored in human subjects.

Indexed as

Immunotherapy, AdoptiveVirus ActivationAntigens, ViralCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedCoculture TechniquesCytomegalovirusCytotoxicity, ImmunologicForkhead Transcription FactorsHematopoietic Stem Cell TransplantationHerpesvirus 6, HumanHumansImmunocompromised HostImmunodominant EpitopesLymphocyte ActivationAntigens, ViralForkhead Transcription FactorsFOXP3 protein, humanImmunodominant Epitopes

Identifiers

PMID23152545
PMCPMC3709638
OpenAlexW1968577431

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.