Evidence map›Paper›PMID 34975869›Full record

ReviewFrontiers in immunology2021

Strategies to Circumvent the Side-Effects of Immunotherapy Using Allogeneic CAR-T Cells and Boost Its Efficacy: Results of Recent Clinical Trials.

Sergei Smirnov, Alexey Petukhov, Ksenia Levchuk, Sergey Kulemzin, Alena Staliarova, Kirill Lepik, Oleg Shuvalov, Andrey Zaritskey, Alexandra Daks, Olga Fedorova

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Emerging strategies to reduce the side effects of CAR-T cell therapy: focusing on gene editing and nanotechnology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  14. Progress on methods of T lymphocyte developmentZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2022
    Review
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  16. Precision medicine: In vivo CAR therapy as a showcase for receptor-targeted vector platforms.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
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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

10 authors.

Sergei SmirnovAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.
Alexey PetukhovAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.
Ksenia LevchukAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.
Sergey KulemzinAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.
Alena StaliarovaBelarusian Research Center for Pediatric Oncology, Hematology and Immunology, Oncological Department 3, Borovliani, Minsk Region, Belarus.
Kirill LepikRM Gorbacheva Research Institute of Pediatric Oncology, Hematology and Transplantation, Chemotherapy and Bone Marrow Transplantation Department, Saint Petersburg, Russia.
Oleg ShuvalovInstitute of Cytology, Laboratory of Gene Expression Regulation, Russian Academy of Sciences, Saint Petersburg, Russia.
Andrey ZaritskeyAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.
Alexandra DaksAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.
Olga FedorovaAlmazov National Medical Research Centre, Personalized Medicine Centre, Saint Petersburg, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the outstanding results of treatment using autologous chimeric antigen receptor T cells (CAR-T cells) in hematological malignancies, this approach is endowed with several constraints. In particular, profound lymphopenia in some patients and the inability to manufacture products with predefined properties or set of cryopreserved batches of cells directed to different antigens in advance. Allogeneic CAR-T cells have the potential to address these issues but they can cause life-threatening graft-versus-host disease or have shorter persistence due to elimination by the host immune system. Novel strategies to create an "off the shelf" allogeneic product that would circumvent these limitations are an extensive area of research. Here we review CAR-T cell products pioneering an allogeneic approach in clinical trials.

Indexed as

Antigens, CD19Clinical Trials as TopicGene EditingGraft vs Host DiseaseHumansImmunotherapy, AdoptiveInduced Pluripotent Stem CellsKiller Cells, NaturalReceptors, Antigen, T-CellReceptors, Chimeric AntigenAntigens, CD19CD19 molecule, humanReceptors, Antigen, T-CellReceptors, Chimeric AntigenallogeneicCAR (chimeric antigen receptor)chimericclinicalGvHDreceptorT celltrials

Identifiers

PMID34975869
PMCPMC8714645

What OpenQuestion holds

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LicenceCC BY
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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.