Evidence map›Paper›PMID 36680242›Full record

ArticleViruses2023

Development of HIV-Resistant CAR T Cells by CRISPR/Cas-Mediated CAR Integration into the

Frederik Holm Rothemejer, Nanna Pi Lauritsen, Anna Karina Juhl, Mariane Høgsbjerg Schleimann, Saskia König, Ole Schmeltz Søgaard, Rasmus O Bak, Martin Tolstrup

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.4field-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

23 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. 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
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. CRISPR/Cas9 for achieving postintervention HIV control.Current opinion in HIV and AIDS · 2025
    Review
  14. Review
  15. Turning "trashed" genomic loci into treasurable sites for integrating chimeric antigen receptors in T and NK cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  16. Article
  17. Review
  18. Current Non-Viral-Based Strategies to Manufacture CAR-T Cells.International journal of molecular sciences · 2024
    Review
  19. Accelerating Diverse Cell-Based Therapies Through Scalable Design.Annual review of chemical and biomolecular engineering · 2024
    Review
  20. 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

8 authors at 1 institution in 1 country.

Frederik Holm RothemejerDepartment of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.ORCID 0000-0002-4826-0704
Nanna Pi LauritsenDepartment of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Anna Karina JuhlDepartment of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.ORCID 0000-0001-6079-5173
Mariane Høgsbjerg SchleimannDepartment of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Saskia KönigDepartment of Biomedicine, Aarhus University, 8200 Aarhus, Denmark.
Ole Schmeltz SøgaardDepartment of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.
Rasmus O BakDepartment of Biomedicine, Aarhus University, 8200 Aarhus, Denmark.ORCID 0000-0002-7383-0297
Martin TolstrupDepartment of Clinical Medicine, Aarhus University, 8200 Aarhus, Denmark.ORCID 0000-0001-7020-5173
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adoptive immunotherapy using chimeric antigen receptor (CAR) T cells has been highly successful in treating B cell malignancies and holds great potential as a curative strategy for HIV infection. Recent advances in the use of anti-HIV broadly neutralizing antibodies (bNAbs) have provided vital information for optimal antigen targeting of CAR T cells. However, CD4+ CAR T cells are susceptible to HIV infection, limiting their therapeutic potential. In the current study, we engineered HIV-resistant CAR T cells using CRISPR/Cas9-mediated integration of a CAR cassette into the

Indexed as

HIV-1HIV InfectionsAnimalsCRISPR-Cas SystemsHIV AntibodiesLeukocytes, MononuclearMiceT-LymphocytesHIV AntibodiesCAR T cellsCRISPR/Cas9HIVhumanized mice

Identifiers

PMID36680242
PMCPMC9862650
OpenAlexW4315498885

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.