Evidence map›Paper›PMID 37419996›Full record

ReviewArchivum immunologiae et therapiae experimentalis2023

In Situ Programming of CAR-T Cells: A Pressing Need in Modern Immunotherapy.

Marta Śledź, Alicja Wojciechowska, Radosław Zagożdżon, Beata Kaleta

Erratum issuedAbstract readReview
In one paragraph

Review in Archivum immunologiae et therapiae experimentalis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Delivery platforms forFrontiers in immunology · 2026
    Review
  3. Frontiers in immunology · 2026
    Review
  4. Review
  5. CAR-T Cell Therapy for Autoimmune Kidney Diseases: Where Do We Stand Now?International journal of molecular sciences · 2025
    Review
  6. Review
  7. Application of nanomedicines in tumor immunotherapy.Journal of molecular cell biology · 2025
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Marta ŚledźDepartment of Clinical Immunology, Medical University of Warsaw, Warsaw, Poland.ORCID http://orcid.org/0000-0002-4497-3096
Alicja WojciechowskaDepartment of Clinical Immunology, Medical University of Warsaw, Warsaw, Poland.ORCID http://orcid.org/0009-0001-8720-8204
Radosław ZagożdżonDepartment of Clinical Immunology, Medical University of Warsaw, Warsaw, Poland.ORCID http://orcid.org/0000-0002-7957-2372
Beata KaletaDepartment of Clinical Immunology, Medical University of Warsaw, Warsaw, Poland. beata.kaleta@wum.edu.pl.ORCID http://orcid.org/0000-0002-0697-2594

Funding

Agencja Badań Medycznych 2020/ABM/04/00002-00
6 · The paper itself

Abstract

Chimeric antigen receptor-T (CAR-T) cell-based therapy has become a successful option for treatment of numerous hematological malignancies, but also raises hope in a range of non-malignant diseases. However, in a traditional approach, generation of CAR-T cells is associated with the separation of patient's lymphocytes, their in vitro modification, and expansion and infusion back into patient's bloodstream. This classical protocol is complex, time-consuming, and expensive. Those problems could be solved by successful protocols to produce CAR-T cells, but also CAR-natural killer cells or CAR macrophages, in situ, using viral platforms or non-viral delivery systems. Moreover, it was demonstrated that in situ CAR-T induction may be associated with reduced risk of the most common toxicities associated with CAR-T therapy, such as cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, and "on-target, off-tumor" toxicity. This review aims to summarize the current state-of-the-art and future perspectives for the in situ-produced CAR-T cells. Indeed, preclinical work in this area, including animal studies, raises hope for prospective translational development and validation in practical medicine of strategies for in situ generation of CAR-bearing immune effector cells.

Indexed as

Receptors, Chimeric AntigenAnimalsImmunotherapyImmunotherapy, AdoptiveNeurotoxicity SyndromesProspective StudiesReceptors, Antigen, T-CellT-Lymphocytescell-associated neurotoxicityReceptors, Antigen, T-CellReceptors, Chimeric AntigenAdoptive cellular therapyCAR-T cellsGene-editing toolsIn-situ generation

Identifiers

PMID37419996
PMCPMC10329070

What OpenQuestion holds

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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.