Evidence map›Paper›PMID 40726984›Full record

ReviewFrontiers in immunology2025

Future perspectives on novel CAR-T therapeutics beyond CD19 and BCMA in onco-hematology.

Alina Ershova, Alexandra Goldaeva, Alena Staliarova, Emil Bulatov, Alexey Petukhov, Nikolai Barlev

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

6 authors.

Alina Ershova *Laboratory of Molecular Oncology, National Laboratory Astana, Astana, Kazakhstan.
Alexandra Goldaeva *International institute "Solution Chemistry of Advanced Materials and Technologies" (SCAMT), ITMO University, Saint Petersburg, Russia.
Alena StaliarovaDr. Sergey Berezin Medical Institute (MIBS), Saint Petersburg, Russia.
Emil BulatovInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Alexey PetukhovLaboratory of Molecular Oncology, National Laboratory Astana, Astana, Kazakhstan.
Nikolai BarlevLaboratory of Molecular Oncology, National Laboratory Astana, Astana, Kazakhstan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CAR-T cell therapy is a type of adoptive immune therapy that relies on the specific targeting of cytotoxic T-cells to eliminate the malfunctioning cells in the body. Genetic engineering allows the generation of an almost infinite variety of chimeric antigen receptors (CAR) to ensure specificity for antigens on the surface of target cells. Therefore, CAR-T appears to be a powerful and versatile therapy for the treatment of various diseases, including cancer. Recently, CAR-T has emerged as a significant advancement in the management of hematological tumors, particularly B-cell malignancies, mainly due to the presence of specific antigens such as CD19 and BCMA. As a result, the market for CAR-T therapy is experiencing significant growth. However, the problem of relapses remains and warrants the search for new therapeutic approaches, including CAR-T technology. In this case, one of the major challenges is finding and evaluating new targets for CAR-T in terms of their likelihood of success. Here we propose a set of established criteria for the evaluation of potential targets for CAR-T cell therapy to treat hematological malignancies. These criteria include assessing the target in terms of its biological characteristics, such as expression level, cellular localization, tissue specificity, and clinical aspects, including unmet clinical needs and the success of clinical trials. Using these criteria, we validate our prediction of the next CAR-T cell therapy targets that will likely emerge soon.

Indexed as

Antigens, CD19B-Cell Maturation AntigenHematologic NeoplasmsImmunotherapy, AdoptiveReceptors, Antigen, T-CellReceptors, Chimeric AntigenAnimalsHumansAntigens, CD19B-Cell Maturation AntigenCD19 molecule, humanReceptors, Antigen, T-CellReceptors, Chimeric AntigenCAR-T targetCAR-T therapychimeric antigen receptorhematological malignanciesoncology

Identifiers

PMID40726984
PMCPMC12301417

What OpenQuestion holds

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Registered trials

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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.