Evidence map›Paper›PMID 33008894›Full record

ArticleScience advances2020

Granzyme B nanoreporter for early monitoring of tumor response to immunotherapy.

Anh Nguyen, Anujan Ramesh, Sahana Kumar, Dipika Nandi, Anthony Brouillard, Alexandria Wells, Leonid Pobezinsky, Barbara Osborne, Ashish A Kulkarni

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 78 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Anh NguyenDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA, USA.ORCID 0000-0002-2069-9352
Anujan RameshDepartment of Biomedical Engineering, University of Massachusetts, Amherst, MA, USA.
Sahana KumarDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA, USA.ORCID 0000-0002-3295-3346
Dipika NandiDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA.
Anthony BrouillardDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA, USA.ORCID 0000-0002-9898-8955
Alexandria WellsDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA.ORCID 0000-0001-9799-8353
Leonid PobezinskyDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA.ORCID 0000-0002-6115-3559
Barbara OsborneDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA.ORCID 0000-0001-8255-0556
Ashish A KulkarniDepartment of Chemical Engineering, University of Massachusetts, Amherst, MA, USA. akulkarni@engin.umass.edu.ORCID 0000-0002-5713-2202
University of Massachusetts Amherst · US

Funding

Biotechnology Training Program in Applied Life SciencesT32GM135096 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Jeanne Ann Hardy, Ashish A. Kulkarni · 2020 to 2026
$3.9M
Defining post-transcriptional mechanisms that control CD8 T cell longevity, proliferation and differentiationR01AI146188 · NIAID · UNIVERSITY OF MASSACHUSETTS AMHERST · PI POBEZINSKIY, LEONID · 2020 to 2024
$2.7M
Cellular Engineering Biotechnology Training ProgramT32GM108556 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI HARDY, JEANNE ANN, PEYTON, SHELLY R. · 2015 to 2019
$766k
NIAID NIH HHS R01 AI146188NIGMS NIH HHS T32 GM108556NIGMS NIH HHS T32 GM135096
6 · The paper itself

Abstract

Despite recent advancements in cancer immunotherapy, accurate monitoring of its efficacy is challenging due to heterogeneous immune responses. Conventional imaging techniques lack the sensitivity and specificity for early response assessment. In this study, we designed a granzyme B (GrB) nanoreporter (GNR) that can deliver an immune checkpoint inhibitor to the tumor and track time-sensitive GrB activity as a direct way to monitor initiation of effective immune responses. Anti-programmed death-ligand 1 (PD-L1) antibody-conjugated GNRs inhibited PD-1/PD-L1 interactions efficiently and induced T cell-mediated GrB release that can be imaged using activatable imaging probe. GNRs enabled real-time immunotherapy response monitoring in a tumor-bearing mice model and distinguished between highly responsive and poorly responsive tumors. Furthermore, increasing doses resulted in a better response and enhanced sensitivity in poorly responsive tumors. These findings indicate that GNR has the potential to serve as a tool for sensitive and noninvasive evaluation of immunotherapy efficacy.

Indexed as

B7-H1 AntigenNeoplasmsAnimalsCell Line, TumorGranzymesImmunologic FactorsImmunotherapyMiceT-LymphocytesB7-H1 AntigenGranzymesImmunologic Factors

Identifiers

PMID33008894
PMCPMC7852386
OpenAlexW3089527184

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.