Evidence map›Paper›PMID 36472784›Full record

ArticleDrug delivery and translational research2023

Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages.

Iago Fernández-Mariño, Clément Anfray, Jose Crecente-Campo, Akihiro Maeda, Aldo Ummarino, Carmen Teijeiro-Valiño, Dario Blanco-Martinez, Francis Mpambani, Laurence Poul, Julie Devalliere and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Drug delivery and translational research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

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  12. Emerging immunotherapeutics for immune activation and tolerance.Drug delivery and translational 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

17 authors at 4 institutions in 3 countries.

Iago Fernández-Mariño *Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Campus Vida, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.
Clément Anfray *Laboratory of Cellular Immunology, IRCCS Humanitas Research Hospital, Rozzano-Milan, 20072, Italy.ORCID http://orcid.org/0000-0002-7118-974X
Jose Crecente-Campo *Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Campus Vida, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.ORCID http://orcid.org/0000-0002-8630-5010
Akihiro MaedaLaboratory of Cellular Immunology, IRCCS Humanitas Research Hospital, Rozzano-Milan, 20072, Italy.ORCID http://orcid.org/0000-0003-4797-0314
Aldo UmmarinoLaboratory of Cellular Immunology, IRCCS Humanitas Research Hospital, Rozzano-Milan, 20072, Italy.ORCID http://orcid.org/0000-0002-8623-0338
Carmen Teijeiro-ValiñoNanomag Laboratory, Applied Physics Department, Campus Vida, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.ORCID http://orcid.org/0000-0003-1838-1764
Dario Blanco-MartinezCenter for Research in Molecular Medicine and Chronic Diseases (CiMUS), Campus Vida, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.
Francis Mpambani, Curadigm 60 rue de Wattignies, Paris, 75012, France.
Laurence Poul, Curadigm 60 rue de Wattignies, Paris, 75012, France.
Julie Devalliere, Curadigm 60 rue de Wattignies, Paris, 75012, France.
Matthieu Germain, Curadigm 60 rue de Wattignies, Paris, 75012, France.
Juan CorreaDepartamento de Química Orgánica, Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Universidade de Santiago de Compostela, Jenaro de la Fuente s/n, Santiago de Compostela, 15782, Spain.
Marcos Fernandez-VillamarinDepartamento de Química Orgánica, Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Universidade de Santiago de Compostela, Jenaro de la Fuente s/n, Santiago de Compostela, 15782, Spain.
Paola AllavenaLaboratory of Cellular Immunology, IRCCS Humanitas Research Hospital, Rozzano-Milan, 20072, Italy.ORCID http://orcid.org/0000-0002-6697-6028
Eduardo Fernandez-MegiaDepartamento de Química Orgánica, Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Universidade de Santiago de Compostela, Jenaro de la Fuente s/n, Santiago de Compostela, 15782, Spain.ORCID http://orcid.org/0000-0002-0405-4933
María José AlonsoCenter for Research in Molecular Medicine and Chronic Diseases (CiMUS), Campus Vida, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain.ORCID http://orcid.org/0000-0001-7187-9567
Fernando Torres AndónCenter for Research in Molecular Medicine and Chronic Diseases (CiMUS), Campus Vida, Universidade de Santiago de Compostela, Santiago de Compostela, 15782, Spain. fernando.torres.andon@usc.es.ORCID http://orcid.org/0000-0001-9235-1278
Universidade de Santiago de Compostela · ESGroupement d'Intérêt Economique · FRIRCCS Humanitas Research Hospital · ITCenter for Research in Molecular Medicine and Chronic Diseases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated macrophages (TAMs), a class of immune cells that play a key role in tumor immunosuppression, are recognized as important targets to improve cancer prognosis and treatment. Consequently, the engineering of drug delivery nanocarriers that can reach TAMs has acquired special relevance. This work describes the development and biological evaluation of a panel of hyaluronic acid (HA) nanocapsules (NCs), with different compositions and prepared by different techniques, designed to target macrophages. The results showed that plain HA NCs did not significantly influence the polarization of M0 and M2-like macrophages towards an M1-like pro-inflammatory phenotype; however, the chemical functionalization of HA with mannose (HA-Man) led to a significant increase of NCs uptake by M2 macrophages in vitro and to an improved biodistribution in a MN/MNCA1 fibrosarcoma mouse model with high infiltration of TAMs. These functionalized HA-Man NCs showed a higher accumulation in the tumor compared to non-modified HA NCs. Finally, the pre-administration of the liposomal liver occupying agent Nanoprimer™ further increased the accumulation of the HA-Man NCs in the tumor. This work highlights the promise shown by the HA-Man NCs to target TAMs and thus provides new options for the development of nanomedicine and immunotherapy-based cancer treatments.

Indexed as

NanocapsulesNeoplasmsAnimalsHyaluronic AcidMannoseMiceTissue DistributionTumor-Associated MacrophagesHyaluronic AcidMannoseNanocapsulesCancerHyaluronic acidMannoseNanoprimerPolymeric nanocapsulesTumor-associated macrophages

Identifiers

PMID36472784
PMCPMC10238357
OpenAlexW4310772613

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.