Evidence map›Paper›PMID 33818299›Full record

ArticlemAbs

TNB-486 induces potent tumor cell cytotoxicity coupled with low cytokine release in preclinical models of B-NHL.

Harbani K Malik-Chaudhry, Kirthana Prabhakar, Harshad S Ugamraj, Andrew A Boudreau, Benjamin Buelow, Kevin Dang, Laura M Davison, Katherine E Harris, Brett Jorgensen, Heather Ogana and 7 more

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. T cell engagers in autoimmune diseases.Nature reviews. Immunology · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Multi-targeted immunotherapeutics to treat B cell malignancies.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Review
  17. Article
  18. Review
  19. Review
  20. Review
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

17 authors at 1 institution in 1 country.

Harbani K Malik-ChaudhryTeneobio, Inc., Newark, CA, United States.ORCID 0000-0002-2804-2697
Kirthana PrabhakarTeneobio, Inc., Newark, CA, United States.
Harshad S UgamrajTeneobio, Inc., Newark, CA, United States.
Andrew A BoudreauTeneobio, Inc., Newark, CA, United States.ORCID 0000-0002-0016-4561
Benjamin BuelowTeneobio, Inc., Newark, CA, United States.
Kevin DangTeneobio, Inc., Newark, CA, United States.
Laura M DavisonTeneobio, Inc., Newark, CA, United States.
Katherine E HarrisTeneobio, Inc., Newark, CA, United States.
Brett JorgensenTeneobio, Inc., Newark, CA, United States.
Heather OganaGraduate Program in Cancer Biology and Genomics, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
Duy PhamTeneobio, Inc., Newark, CA, United States.
Ute SchellenbergerTeneobio, Inc., Newark, CA, United States.ORCID 0000-0002-4809-9383
Wim Van SchootenTeneobio, Inc., Newark, CA, United States.
Roland BuelowTeneobio, Inc., Newark, CA, United States.
Suhasini IyerTeneobio, Inc., Newark, CA, United States.
Nathan D TrinkleinTeneobio, Inc., Newark, CA, United States.
Udaya S RangaswamyTeneobio, Inc., Newark, CA, United States.ORCID 0000-0002-3994-3861
University of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The therapeutic potential of targeting CD19 in B cell malignancies has garnered attention in the past decade, resulting in the introduction of novel immunotherapy agents. Encouraging clinical data have been reported for T cell-based targeting agents, such as anti-CD19/CD3 bispecific T-cell engager blinatumomab and chimeric antigen receptor (CAR)-T therapies, for acute lymphoblastic leukemia and B cell non-Hodgkin lymphoma (B-NHL). However, clinical use of both blinatumomab and CAR-T therapies has been limited due to unfavorable pharmacokinetics (PK), significant toxicity associated with cytokine release syndrome and neurotoxicity, and manufacturing challenges. We present here a fully human CD19xCD3 bispecific antibody (TNB-486) for the treatment of B-NHL that could address the limitations of the current approved treatments. In the presence of CD19+ target cells and T cells, TNB-486 induces tumor cell lysis with minimal cytokine release, when compared to a positive control.

Indexed as

AnimalsAntibodies, BispecificAntibodies, Monoclonal, HumanizedAntigens, CD19Antineoplastic Agents, ImmunologicalCD3 ComplexCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCoculture TechniquesCytokinesCytotoxicity, ImmunologicHumansK562 CellsLymphocyte ActivationLymphoma, Non-HodgkinMacaca fascicularisAntibodies, BispecificAntibodies, Monoclonal, HumanizedAntigens, CD19Antineoplastic Agents, ImmunologicalCD19 molecule, humanCD3 ComplexCytokinesBispecific antibodyCD19XCD3cytokine release syndromelow cytokine releaseT-cell engagerTNB-486

Identifiers

PMID33818299
PMCPMC8023237
OpenAlexW3145562791

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.