Evidence map›Paper›PMID 39103055›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2024

Systemically targeting monocytic myeloid-derived suppressor cells using dendrimers and their cell-level biodistribution kinetics.

Chad A Littrell, Gregory P Takacs, Chenikkayala Siva Sankara, Alexandra Sherman, Kai A Rubach, Julia S Garcia, Coral A Bell, Tejashwini Lnu, Jeffrey K Harrison, Fan Zhang

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

10 authors.

Chad A LittrellDepartment of Pharmacology & Therapeutics, University of Florida College of Medicine, Gainesville, FL, United States.
Gregory P TakacsDepartment of Pharmacology & Therapeutics, University of Florida College of Medicine, Gainesville, FL, United States.
Chenikkayala Siva SankaraDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, FL, United States.
Alexandra ShermanDepartment of Pharmacology & Therapeutics, University of Florida College of Medicine, Gainesville, FL, United States.
Kai A RubachDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, FL, United States.
Julia S GarciaDepartment of Pharmacology & Therapeutics, University of Florida College of Medicine, Gainesville, FL, United States.
Coral A BellDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, FL, United States.
Tejashwini LnuDepartment of Chemical Engineering, University of Florida College of Pharmacy, Gainesville, FL, United States.
Jeffrey K HarrisonDepartment of Pharmacology & Therapeutics, University of Florida College of Medicine, Gainesville, FL, United States.
Fan ZhangDepartment of Pharmacology & Therapeutics, University of Florida College of Medicine, Gainesville, FL, United States; Department of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, FL, United States; Department of Chemical Engineering, University of Florida College of Pharmacy, Gainesville, FL, United States. Electronic address: fzhang1@ufl.edu.

Funding

Targeting CCR2-expressing myeloid cells to overcome immune checkpoint inhibitor resistance in gliomaR01NS108781 · NINDS · UNIVERSITY OF FLORIDA · PI HARRISON, JEFFREY K., MITCHELL, DUANE A. · 2018 to 2022
$1.9M
NINDS NIH HHS R01 NS108781
6 · The paper itself

Abstract

The focus of nanoparticles in vivo trafficking has been mostly on their tissue-level biodistribution and clearance. Recent progress in the nanomedicine field suggests that the targeting of nanoparticles to immune cells can be used to modulate the immune response and enhance therapeutic delivery to the diseased tissue. In the presence of tumor lesions, monocytic-myeloid-derived suppressor cells (M-MDSCs) expand significantly in the bone marrow, egress into peripheral blood, and traffic to the solid tumor, where they help maintain an immuno-suppressive tumor microenvironment. In this study, we investigated the interaction between PAMAM dendrimers and M-MDSCs in two murine models of glioblastoma, by examining the cell-level biodistribution kinetics of the systemically injected dendrimers. We found that M-MDSCs in the tumor and lymphoid organs can efficiently endocytose hydroxyl dendrimers. Interestingly, the trafficking of M-MDSCs from the bone marrow to the tumor contributed to the deposition of hydroxyl dendrimers in the tumor. M-MDSCs showed different capacities of endocytosing dendrimers of different functionalities in vivo. This differential uptake was mediated by the unique serum proteins associated with each dendrimer surface functionality. The results of this study set up the framework for developing dendrimer-based immunotherapy to target M-MDSCs for cancer treatment.

Indexed as

DendrimersMice, Inbred C57BLMyeloid-Derived Suppressor CellsAnimalsCell Line, TumorEndocytosisFemaleGlioblastomaMiceTissue DistributionDendrimersPAMAM StarburstBiodistributionCCR2Cell uptakeGlioblastomaM-MDSCPAMAM dendrimerProtein corona

Identifiers

PMID39103055
PMCPMC11416312

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.