Evidence map›Paper›PMID 32295875›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2020

Toxicity Induced by a Bispecific T Cell-Redirecting Protein Is Mediated by Both T Cells and Myeloid Cells in Immunocompetent Mice.

Claire Godbersen-Palmer, Tiffany A Coupet, Zakaria Grada, Samuel C Zhang, Charles L Sentman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2020. 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
1.2field-weighted citation impact, top 19% 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, 17 citations in OpenAlex.

  1. Article
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  5. Dissecting the Mechanisms Underlying the Cytokine Release Syndrome (CRS) Mediated by T-Cell Bispecific Antibodies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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 2 institutions in 1 country.

Claire Godbersen-PalmerCenter for Synthetic Immunity, Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756; and.
Tiffany A CoupetCenter for Synthetic Immunity, Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756; and.
Zakaria GradaDepartment of Pathology, Dartmouth-Hitchcock Medical Center, Lebanon, NH 03756.ORCID 0000-0002-2224-5979
Samuel C ZhangCenter for Synthetic Immunity, Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756; and.ORCID 0000-0003-2688-7781
Charles L SentmanCenter for Synthetic Immunity, Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756; and charles.sentman@dartmouth.edu.ORCID 0000-0003-3976-5847
Dartmouth College · USDartmouth–Hitchcock Medical Center · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
Molecular and Cellular Biology at DartmouthT32GM008704 · NIGMS · DARTMOUTH COLLEGE · PI COMPTON, DUANE A. · 1998 to 2018
$6.8M
A novel NKG2D-specific BiTE cancer immunotherapyR01CA164178 · NCI · DARTMOUTH COLLEGE · PI SENTMAN, CHARLES L. · 2013 to 2017
$1.7M
NCI NIH HHS P30 CA023108NCI NIH HHS R01 CA164178NIAID NIH HHS T32 AI007363NIGMS NIH HHS T32 GM008704
6 · The paper itself

Abstract

Bispecific T cell engagers have demonstrated clinical efficacy; however, their use can be accompanied by severe toxicity. Mechanistic understanding of these toxicities is limited by a lack of suitable immunocompetent preclinical models. In this study, we describe an immunocompetent mouse tumor model that exhibits bispecific T cell engager-induced toxicity and recapitulates key features similar to those in human cytokine release syndrome. In this study, toxicity occurred between the second and fourth injections of an NK Group 2D bispecific T cell engager protein. Symptoms were transient, peaking 3-4 h after treatment and resolving by 8 h. Mice developed weight loss, elevated plasma cytokines, a significant reduction in spleen white pulp, and lymphocyte infiltration in the liver. Systemic cellular immune changes also occurred; notably, an increase in CD8

Indexed as

AnimalsCD3 ComplexCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorClodronic AcidColonic NeoplasmsCytokine Release SyndromeDisease Models, AnimalDrug-Related Side Effects and Adverse ReactionsHumansInterferon-gammaLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutCD3 ComplexClodronic AcidInterferon-gammaKlrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily KReceptors, Chimeric Antigen

Identifiers

PMID32295875
PMCPMC7304495
OpenAlexW3016667495

What OpenQuestion holds

Textmetadata
LicenceTDM
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.