Evidence map›Paper›PMID 28670716›Full record

ArticleImmunology2017

Adoptive transfer of murine T cells expressing a chimeric-PD1-Dap10 receptor as an immunotherapy for lymphoma.

Adam Lynch, William Hawk, Emily Nylen, Sean Ober, Pierre Autin, Amorette Barber

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Chimeric non-antigen receptors in T cell-based cancer therapy.Journal for immunotherapy of cancer · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. CARs: Beyond T Cells and T Cell-Derived Signaling Domains.International journal of molecular sciences · 2020
    Review
  14. Review
  15. 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

6 authors at 1 institution in 1 country.

Adam LynchDepartment of Biological and Environmental Sciences, Longwood University, Farmville, VA, USA.
William HawkDepartment of Biological and Environmental Sciences, Longwood University, Farmville, VA, USA.
Emily NylenDepartment of Biological and Environmental Sciences, Longwood University, Farmville, VA, USA.
Sean OberDepartment of Biological and Environmental Sciences, Longwood University, Farmville, VA, USA.
Pierre AutinDepartment of Biological and Environmental Sciences, Longwood University, Farmville, VA, USA.
Amorette BarberDepartment of Biological and Environmental Sciences, Longwood University, Farmville, VA, USA.ORCID 0000-0001-9128-7606
Longwood University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adoptive transfer of T cells is a promising cancer therapy and expression of chimeric antigen receptors can enhance tumour recognition and T-cell effector functions. The programmed death protein 1 (PD1) receptor is a prospective target for a chimeric antigen receptor because PD1 ligands are expressed on many cancer types, including lymphoma. Therefore, we developed a murine chimeric PD1 receptor (chPD1) consisting of the PD1 extracellular domain fused to the cytoplasmic domain of CD3ζ. Additionally, chimeric antigen receptor therapies use various co-stimulatory domains to enhance efficacy. Hence, the inclusion of a Dap10 or CD28 co-stimulatory domain in the chPD1 receptor was compared to determine which domain induced optimal anti-tumour immunity in a mouse model of lymphoma. The chPD1 T cells secreted pro-inflammatory cytokines and lysed RMA lymphoma cells. Adoptive transfer of chPD1 T cells significantly reduced established tumours and led to tumour-free survival in lymphoma-bearing mice. When comparing chPD1 receptors containing a Dap10 or CD28 domain, both receptors induced secretion of pro-inflammatory cytokines; however, chPD1-CD28 T cells also secreted anti-inflammatory cytokines whereas chPD1-Dap10 T cells did not. Additionally, chPD1-Dap10 induced a central memory T-cell phenotype compared with chPD1-CD28, which induced an effector memory phenotype. The chPD1-Dap10 T cells also had enhanced in vivo persistence and anti-tumour efficacy compared with chPD1-CD28 T cells. Therefore, adoptive transfer of chPD1 T cells could be a novel therapy for lymphoma and inclusion of the Dap10 co-stimulatory domain in chimeric antigen receptors may induce a preferential cytokine profile and T-cell differentiation phenotype for anti-tumour therapies.

Indexed as

Adoptive TransferAnimalsCD28 AntigensCD3 ComplexCells, CulturedCytokinesCytotoxicity, ImmunologicGenetic TherapyGenotypeHumansImmunologic MemoryInflammation MediatorsLeukocyte Common AntigensLymphoma, T-CellMaleMice, CongenicCD28 AntigensCD3 antigen, zeta chainCD3 ComplexCytokinesHcst protein, mouseInflammation MediatorsLeukocyte Common AntigensPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorPtprc protein, mouseReceptors, ImmunologicCD8 T cellchimeric antigen receptorDap10immunotherapylymphoma

Identifiers

PMID28670716
PMCPMC5629437
OpenAlexW2728578251

What OpenQuestion holds

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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.