Evidence map›Paper›PMID 24751697›Full record

ArticlePloS one2014

Characterization of a novel single-chain bispecific antibody for retargeting of T cells to tumor cells via the TCR co-receptor CD8.

Irene Michalk, Anja Feldmann, Stefanie Koristka, Claudia Arndt, Marc Cartellieri, Armin Ehninger, Gerhard Ehninger, Michael P Bachmann

Abstract read
In one paragraph

Article in PloS one, 2014. 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
–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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Engaging T cells for cleanup.Frontiers in immunology · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Bispecific Immunomodulatory Antibodies for Cancer Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  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

8 authors.

Irene MichalkInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany.
Anja FeldmannInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany; Helmholtz Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Department of Radioimmunology, Dresden, Germany.
Stefanie KoristkaInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany.
Claudia ArndtInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany.
Marc CartellieriInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany; Helmholtz Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Department of Radioimmunology, Dresden, Germany.
Armin EhningerInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany; Medical Clinic and Polyclinic I, University Hospital 'Carl Gustav Carus', TU Dresden, Dresden, Germany.
Gerhard EhningerMedical Clinic and Polyclinic I, University Hospital 'Carl Gustav Carus', TU Dresden, Dresden, Germany.
Michael P BachmannInstitute of Immunology, Medical Faculty 'Carl Gustav Carus', TU Dresden, Dresden, Germany; Helmholtz Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Department of Radioimmunology, Dresden, Germany; Center for Regenerative Therapies Dresden, TU Dresden, Dresden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is currently growing interest in retargeting of effector T cells to tumor cells via bispecific antibodies (bsAbs). Usually, bsAbs are directed on the one hand to the CD3 complex of T cells and on the other hand to a molecule expressed on the surface of the target cell. A bsAb-mediated cross-linkage via CD3 leads to an activation of CD8+ T cells and consequently to killing of the target cells. In parallel, CD4+ T cells including TH1, TH2, TH17 cells and even regulatory T cells (Tregs) will be activated as well. Cytokines produced by CD4+ T cells can contribute to severe side effects e. g. life-threatening cytokine storms and, thinking of the immunosupressive function of Tregs, can even be counterproductive. Therefore, we asked whether or not it is feasible to limit retargeting to CD8+ T cells e. g. via targeting of the co-receptor CD8 instead of CD3. In order to test for proof of concept, a novel bsAb with specificity for CD8 and a tumor-associated surface antigen was constructed. Interestingly, we found that pre-activated (but not freshly isolated) CD8+ T cells can be retargeted via CD8-engaging bsAbs leading to an efficient lysis of target cells.

Indexed as

AnimalsAntibodies, BispecificCD3 ComplexCD8 AntigensCD8-Positive T-LymphocytesCell LineCell SeparationCross-Linking ReagentsCytokinesCytotoxicity, ImmunologicHumansLymphocyte ActivationMiceNeoplasmsProtein BindingReceptors, Antigen, T-CellAntibodies, BispecificCD3 ComplexCD8 AntigensCross-Linking ReagentsCytokinesReceptors, Antigen, T-CellSingle-Chain Antibodies

Identifiers

PMID24751697
PMCPMC3994066

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Registered trials

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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.