Evidence map›Paper›PMID 34027092›Full record

ArticleBioengineering & translational medicine2021

Targeted systemic dendrimer delivery of CSF-1R inhibitor to tumor-associated macrophages improves outcomes in orthotopic glioblastoma.

Kevin Liaw, Rajsekhar Reddy, Anjali Sharma, Jiangyu Li, Michelle Chang, Rishi Sharma, Sebastian Salazar, Sujatha Kannan, Rangaramanujam M Kannan

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 38 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.

Kevin LiawDepartment of Chemical and Biomolecular Engineering Johns Hopkins University Baltimore Maryland USA.
Rajsekhar ReddyCenter for Nanomedicine, Department of Ophthalmology Johns Hopkins Medicine Baltimore Maryland USA.ORCID https://orcid.org/0000-0001-6815-6149
Anjali SharmaCenter for Nanomedicine, Department of Ophthalmology Johns Hopkins Medicine Baltimore Maryland USA.
Jiangyu LiDepartment of Biomedical Engineering Johns Hopkins University Baltimore Maryland USA.
Michelle ChangDepartment of Chemical and Biomolecular Engineering Johns Hopkins University Baltimore Maryland USA.
Rishi SharmaCenter for Nanomedicine, Department of Ophthalmology Johns Hopkins Medicine Baltimore Maryland USA.
Sebastian SalazarDepartment of Biomedical Engineering Johns Hopkins University Baltimore Maryland USA.
Sujatha KannanAnesthesiology and Critical Care Medicine Johns Hopkins Medicine Baltimore Maryland USA.
Rangaramanujam M KannanDepartment of Chemical and Biomolecular Engineering Johns Hopkins University Baltimore Maryland USA.ORCID https://orcid.org/0000-0002-3712-7836
Johns Hopkins University · US

Funding

Nanotherapies for the treatment of neurodevelopmental disorders.R01EB018306 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI RANGARAMANUJAM, KANNAN · 2014 to 2017
$1.5M
NIBIB NIH HHS R01 EB018306
6 · The paper itself

Abstract

Glioblastoma is the most common and aggressive form of primary brain cancer, with median survival of 16-20 months and a 5-year survival rates of <5%. Recent advances in immunotherapies have shown that addressing the tumor immune profile by targeting the colony-stimulating factor 1 (CSF-1) signaling pathway of tumor-associated macrophages (TAMs) has the potential to improve glioblastoma therapy. However, such therapies have shown limited successes in clinical translation partially due to lack of specific cell targeting in solid tumors and systemic toxicity. In this study, we present a novel hydroxyl dendrimer-mediated immunotherapy to deliver CSF-1R inhibitor BLZ945 (D-BLZ) from systemic administration selectively to TAMs in glioblastoma brain tumors to repolarize the tumor immune environment in a localized manner. We show that conjugation of BLZ945 to dendrimers enables sustained release in intracellular and intratumor conditions. We demonstrate that a single systemic dose of D-BLZ targeted to TAMs decreases pro-tumor expression in TAMs and promotes cytotoxic T cell infiltration, resulting in prolonged survival and ameliorated disease burden compared to free BLZ945. Our results demonstrate that dendrimer-drug conjugates can facilitate specific, localized manipulation of tumor immune responses from systemic administration by delivering immunotherapies selectively to TAMs, thereby improving therapeutic efficacy while reducing off-target effects.

Indexed as

dendrimerglioblastomaimmunotherapysystemictargeted deliverytumor‐associated macrophage

Identifiers

PMID34027092
PMCPMC8126814
OpenAlexW3108272450

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.