Evidence map›Paper›PMID 39311380›Full record

ArticleAntibodies (Basel, Switzerland)2024

A Novel Tetravalent Bispecific Immune Cell Engager Activates Natural Killer Cells to Kill Cancer Cells without Mediating Fratricide.

Ge Yang, Shahryar Khoshtinat Nikkhoi, Hajar Owji, Geng Li, Mohammad Massumi, Jessica Cervelli, Venu Gopal Vandavasi, Arash Hatefi

Abstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Ge YangDepartment of Pharmaceutics, Rutgers University, Piscataway, NJ 08854, USA.ORCID 0000-0002-2624-4412
Shahryar Khoshtinat NikkhoiDepartment of Pharmaceutics, Rutgers University, Piscataway, NJ 08854, USA.ORCID 0000-0002-7069-4111
Hajar OwjiDepartment of Pharmaceutics, Rutgers University, Piscataway, NJ 08854, USA.
Geng LiDepartment of Pharmaceutics, Rutgers University, Piscataway, NJ 08854, USA.
Mohammad MassumiDepartment of Pharmaceutics, Rutgers University, Piscataway, NJ 08854, USA.
Jessica CervelliEnvironmental and Occupational Health Science Institute, Flow Cytometry Core Facility, Rutgers University, Piscataway, NJ 08854, USA.
Venu Gopal VandavasiDepartment of Chemistry, Biophysics Core Facility, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-8894-1395
Arash HatefiDepartment of Pharmaceutics, Rutgers University, Piscataway, NJ 08854, USA.ORCID 0000-0003-4611-7469

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Rutgers Optimizes Innovation (ROI) ProgramU01HL150852 · NHLBI · RUTGERS BIOMEDICAL/HEALTH SCIENCES-RBHS · PI LIBUTTI, STEVEN K., PANETTIERI, REYNOLD ALEXANDER · 2019 to 2022
$4.4M
Stem Cell-based Platform for Targeted Enzyme/Prodrug Therapy of Recurrent Ovarian CancerR01CA251438 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI HATEFI, ARASH · 2021 to 2025
$1.9M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA251438NCI NIH HHS R01CA251438NHLBI NIH HHS U01 HL150852NHLBI/Rutgers HealthAdvance U01HL150852
6 · The paper itself

Abstract

We previously reported the structure, affinity, and anticancer activity of a bivalent bispecific natural killer cell engager (BiKE) composed of one anti-CD16a VHH and one anti-HER2 VHH fused via a linker. In this study, we explored the engineering of a tetravalent BiKE by fusing two anti-CD16a and two anti-HER2 VHHs in tandem, using bivalent BiKE as a template. The tetravalent BiKE was genetically engineered, and its tertiary structure was predicted using in silico modeling. The antigen binding and affinity of the tetravalent BiKE were assessed using ELISA, flow cytometry, and biolayer interferometry. The ability of the BiKEs to kill cancer cells was evaluated through classical and residual antibody-dependent cellular cytotoxicity (ADCC) assays. Additionally, we investigated the potential for NK cell fratricide via CD16a-CD16a crosslinking. Our results revealed that the tetravalent BiKE exhibited at least 100-fold higher affinity toward its target antigens compared to its bivalent counterpart. The residual ADCC assay indicated that the tetravalent BiKE was more effective in killing cancer cells than the bivalent BiKE, attributable to its lower K

Indexed as

BiKECD16adaratumumabfratricideimmune cell engagerlaNK92multi-paratope antibodytetravalent bispecific antibodyVHH

Identifiers

PMID39311380
PMCPMC11417942

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.