Evidence map›Paper›PMID 29152058›Full record

ArticleOncotarget2017

Effective control of acute myeloid leukaemia and acute lymphoblastic leukaemia progression by telomerase specific adoptive T-cell therapy.

Sara Sandri, Francesco De Sanctis, Alessia Lamolinara, Federico Boschi, Ornella Poffe, Rosalinda Trovato, Alessandra Fiore, Sara Sartori, Andrea Sbarbati, Attilio Bondanza and 8 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Telomerase (Genes · 2021
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Immune escape and immunotherapy of acute myeloid leukemia.The Journal of clinical investigation · 2020
    Review
  17. Antigen Targets for the Development of Immunotherapies in Leukemia.International journal of molecular sciences · 2019
    Review
  18. Review
  19. Article
  20. Review
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

18 authors at 4 institutions in 2 countries.

Sara Sandri *Department of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Francesco De Sanctis *Department of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Alessia LamolinaraDepartment of Medicine and Aging Science, Center of Excellence on Aging and Translational Medicine (CeSi-Met), G. D'Annunzio University, Chieti-Pescara, Italy.
Federico BoschiDepartment of Computer Science, University of Verona, Verona, Italy.
Ornella PoffeDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Rosalinda TrovatoDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Alessandra FioreDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Sara SartoriDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Andrea SbarbatiDepartment of Neurological and Movement Sciences, University of Verona, Verona, Italy.
Attilio BondanzaInnovative Immunotherapies Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Hospital Scientific Institute, Vita-Salute San Raffaele University, Milano, Italy.
Simone CesaroDepartment of Pediatric Haematology Oncology, University of Verona, Verona, Italy.
Mauro KramperaDepartment of Medicine, University of Verona, Section of Haematology, Verona, Italy.
Maria T ScupoliDepartment of Medicine, University of Verona, Section of Haematology, Verona, Italy.
Michael I NishimuraDepartment of Surgery, Loyola University Medical Center, Maywood, IL, United States.
Manuela IezziDepartment of Medicine and Aging Science, Center of Excellence on Aging and Translational Medicine (CeSi-Met), G. D'Annunzio University, Chieti-Pescara, Italy.
Silvia SartorisDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Vincenzo BronteDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
Stefano UgelDepartment of Medicine, University of Verona, Section of Immunology, Verona, Italy.
University of Verona · ITUniversity of Chieti-Pescara · ITLoyola University Medical Center · USVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomerase (TERT) is a ribonucleoprotein enzyme that preserves the molecular organization at the ends of eukaryotic chromosomes. Since TERT deregulation is a common step in leukaemia, treatments targeting telomerase might be useful for the therapy of hematologic malignancies. Despite a large spectrum of potential drugs, their bench-to-bedside translation is quite limited, with only a therapeutic vaccine in the clinic and a telomerase inhibitor at late stage of preclinical validation. We recently demonstrated that the adoptive transfer of T cell transduced with an HLA-A2-restricted T-cell receptor (TCR), which recognize human TERT with high avidity, controls human B-cell chronic lymphocytic leukaemia (B-CLL) progression without severe side-effects in humanized mice. In the present report, we show the ability of our approach to limit the progression of more aggressive leukemic pathologies, such as acute myeloid leukaemia (AML) and B-cell acute lymphoblastic leukaemia (B-ALL). Together, our findings demonstrate that TERT-based adoptive cell therapy is a concrete platform of T cell-mediated immunotherapy for leukaemia treatment.

Indexed as

acute myeloid leukaemia (AML)adoptive cell therapy (ACT)B-cell acute lymphoblastic leukaemia (B-ALL)TCR-redirected T-cellstelomerase (TERT)

Identifiers

PMID29152058
PMCPMC5675610
OpenAlexW2618311166

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.