Evidence map›Paper›PMID 35042811›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

V-CARMA: A tool for the detection and modification of antigen-specific T cells.

Xi-Zhi J Guo, Stephen J Elledge

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. TIL Therapy in Lung Cancer: Current Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  6. Antigen-specific T cell immunotherapy by in vivo mRNA delivery.bioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. In vivo gene delivery to immune cells.Current opinion in biotechnology · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. 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

2 authors at 1 institution in 1 country.

Xi-Zhi J GuoDivision of Genetics, Brigham and Women's Hospital, Boston, MA 02115.
Stephen J ElledgeDivision of Genetics, Brigham and Women's Hospital, Boston, MA 02115; selledge@genetics.med.harvard.edu.ORCID 0000-0001-7923-6283
Brigham and Women's Hospital · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

T cells promote our body's ability to battle cancers and infectious diseases but can act pathologically in autoimmunity. The recognition of peptides presented by major histocompatibility complex (pMHC) molecules by T cell receptors (TCRs) enables T cell-mediated responses. To modify disease-relevant T cells, new tools to genetically modify T cells and decode their antigen recognition are needed. Here, we present an approach using viruses pseudotyped with peptides loaded on MHC called V-CARMA (Viral ChimAeric Receptor MHC-Antigen) to specifically target T cells expressing cognate TCRs for antigen discovery and T cell engineering. We show that lentiviruses displaying antigens on human leukocyte antigen (HLA) class I and class II molecules can robustly infect CD8

Indexed as

AntigensCD8-Positive T-LymphocytesGenetic EngineeringHistocompatibility Antigens Class IHumansImmunotherapyLentivirusLymphocyte ActivationLymphokinesMajor Histocompatibility ComplexPeptidesReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaReceptors, Chimeric AntigenAntigensantigen-specific helper factorsHistocompatibility Antigens Class ILymphokinesPeptidesReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaReceptors, Chimeric Antigenpeptide-MHC complexpseudotyped lentivirusT cell modification

Identifiers

PMID35042811
PMCPMC8795542
OpenAlexW4206128991

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.