Evidence map›Paper›PMID 15746083›Full record

ArticleBlood2005

Therapeutic potential of a tumor-specific, MHC-unrestricted T-cell receptor expressed on effector cells of the innate and the adaptive immune system through bone marrow transduction and immune reconstitution.

Nehad M Alajez, Jan Schmielau, Mark D Alter, Michael Cascio, Olivera J Finn

Open access · greenAbstract read
In one paragraph

Article in Blood, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Cytotoxic T-lymphocyte immunotherapy for ovarian cancer: a pilot study.Journal of immunotherapy (Hagerstown, Md. : 1997)
    Trial
  2. Article
  3. Transcription-Related Dynamics from Immune Disability into Endogenous Innovation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  4. In Vitro Differentiation of T Cells from Murine Pluripotent Stem Cells.Methods in molecular biology (Clifton, N.J.) · 2019
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Cytokine-induced NK-like T cells: from bench to bedside.Journal of biomedicine & biotechnology · 2010
    Review
  17. Article
  18. Article
  19. Article
  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

5 authors at 1 institution in 1 country.

Nehad M AlajezDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Jan Schmielau
Mark D Alter
Michael Cascio
Olivera J Finn
University of Pittsburgh · US

Funding

T CELL IMMUNITY TO EPITHELIAL TUMOR MUCINSR01CA056103 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINN, OLIVERA J · 1991 to 2013
$3.4M
NCI NIH HHS CA56103
6 · The paper itself

Abstract

T-cell receptor (TCR) with unique major histocompatibility complex (MHC)-unrestricted antigen-binding properties was isolated from a human T-cell clone specific for the tumor antigen MUC1. This TCR binds its epitope on the MUC1 protein without the requirement of processing and presentation. A single-chain Valpha/Vbeta/Cbeta (scTCR) was fused to a CD3 zeta (zeta) chain to allow expression on the surface of cells of the innate (granulocytes, macrophages, natural killer [NK] cells) as well as the adaptive (T and B cells) immune system. To test the ability of the cells of the innate immune system to reject a tumor when provided with a tumor antigen-specific TCR, we reconstituted severe combined immunodeficiency (SCID) mice with bone marrow cells transduced with a retroviral vector encoding this receptor and challenged them with a MUC1-positive human tumor. These mice controlled the growth of the tumor significantly better than the control mice. We performed a similar experiment in immunocompetent mice transgenic for human MUC1. Expression of the TCR on large percentages of cells did not result in infiltration or destruction of tissues expressing MUC1. Reconstituted mice controlled the outgrowth of a MUC1-transfected but not the parental control tumor. scTCR expression appears lifelong, suggesting a successful transduction of the self-renewing stem cells.

Indexed as

Amino Acid SequenceAnimalsAntigens, NeoplasmB-LymphocytesBone Marrow CellsCD3 ComplexCell LineageCell Line, TumorEnzyme-Linked Immunosorbent AssayEpitopesFlow CytometryGranulocytesGreen Fluorescent ProteinsHematopoietic Stem CellsHumansImmune SystemAntigens, NeoplasmCD3 antigen, zeta chainCD3 ComplexEpitopesGreen Fluorescent ProteinsInterleukin-2Mucin-1Receptors, Antigen, T-Cell

Identifiers

PMID15746083
PMCPMC1894994
OpenAlexW2007497663

What OpenQuestion holds

Textmetadata
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.