Evidence map›Paper›PMID 37511628›Full record

ReviewInternational journal of molecular sciences2023

Liver Cell Type-Specific Targeting by Nanoformulations for Therapeutic Applications.

Leonard Kaps, María José Limeres, Paul Schneider, Malin Svensson, Yanira Zeyn, Silvia Fraude, Maximiliano L Cacicedo, Peter R Galle, Stephan Gehring, Matthias Bros

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Metabolic Reprogramming in Cancer Stem Cells.Cancer treatment and research · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. 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 at 1 institution in 1 country.

Leonard KapsI. Department of Medicine, University Medical Center Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
María José LimeresChildren's Hospital, University Medical Center, Langenbeckstrasse 1, 55131 Mainz, Germany.ORCID 0000-0003-2848-4679
Paul SchneiderI. Department of Medicine, University Medical Center Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Malin SvenssonChildren's Hospital, University Medical Center, Langenbeckstrasse 1, 55131 Mainz, Germany.
Yanira ZeynDepartment of Dermatology, University Medical Center Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.ORCID 0000-0002-2501-8149
Silvia FraudeChildren's Hospital, University Medical Center, Langenbeckstrasse 1, 55131 Mainz, Germany.ORCID 0009-0005-9211-2513
Maximiliano L CacicedoChildren's Hospital, University Medical Center, Langenbeckstrasse 1, 55131 Mainz, Germany.ORCID 0000-0002-3144-8794
Peter R GalleI. Department of Medicine, University Medical Center Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Stephan GehringChildren's Hospital, University Medical Center, Langenbeckstrasse 1, 55131 Mainz, Germany.
Matthias BrosDepartment of Dermatology, University Medical Center Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Johannes Gutenberg University Mainz · DE

Funding

Deutsche Forschungsgemeinschaft SFB1066, B15+B17
6 · The paper itself

Abstract

Hepatocytes exert pivotal roles in metabolism, protein synthesis and detoxification. Non-parenchymal liver cells (NPCs), largely comprising macrophages, dendritic cells, hepatic stellate cells and liver sinusoidal cells (LSECs), serve to induce immunological tolerance. Therefore, the liver is an important target for therapeutic approaches, in case of both (inflammatory) metabolic diseases and immunological disorders. This review aims to summarize current preclinical nanodrug-based approaches for the treatment of liver disorders. So far, nano-vaccines that aim to induce hepatitis virus-specific immune responses and nanoformulated adjuvants to overcome the default tolerogenic state of liver NPCs for the treatment of chronic hepatitis have been tested. Moreover, liver cancer may be treated using nanodrugs which specifically target and kill tumor cells. Alternatively, nanodrugs may target and reprogram or deplete immunosuppressive cells of the tumor microenvironment, such as tumor-associated macrophages. Here, combination therapies have been demonstrated to yield synergistic effects. In the case of autoimmune hepatitis and other inflammatory liver diseases, anti-inflammatory agents can be encapsulated into nanoparticles to dampen inflammatory processes specifically in the liver. Finally, the tolerance-promoting activity especially of LSECs has been exploited to induce antigen-specific tolerance for the treatment of allergic and autoimmune diseases.

Indexed as

HepatitisLiver NeoplasmsHepatic Stellate CellsHepatocytesHumansLiverTumor Microenvironmentfibrosishepatitishepatocellular carcinomaKupffer cellliverliver metastasisliver sinusoidal endothelial cellnanoformulationnon-parenchymal cells

Identifiers

PMID37511628
PMCPMC10380755
OpenAlexW4385241573

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.