Evidence map›Paper›PMID 39228913›Full record

ReviewFrontiers in molecular biosciences2024

PBMC-engrafted humanized mice models for evaluating immune-related and anticancer drug delivery systems.

Yoshie Kametani, Ryoji Ito, Yoshiyuki Manabe, Jerzy K Kulski, Toshiro Seki, Hitoshi Ishimoto, Takashi Shiina

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
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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

7 authors.

Yoshie KametaniDepartment of Molecular Life Science, Division of Basic Medical Science, Tokai University School of Medicine, Isehara, Japan.
Ryoji ItoCentral Institute for Experimental Medicine and Life Science (CIEM), Kawasaki, Japan.
Yoshiyuki ManabeDepartment of Chemistry, Graduate School of Science, Osaka University, Osaka, Japan.
Jerzy K KulskiDepartment of Molecular Life Science, Division of Basic Medical Science, Tokai University School of Medicine, Isehara, Japan.
Toshiro SekiDepartment of Internal Medicine, Division of Nephrology, Endocrinology, and Metabolism, Tokai University School of Medicine, Isehara, Japan.
Hitoshi IshimotoDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Isehara, Japan.
Takashi ShiinaDepartment of Molecular Life Science, Division of Basic Medical Science, Tokai University School of Medicine, Isehara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune-related drug delivery systems (DDSs) in humanized mouse models are at the forefront of cancer research and serve as bridges between preclinical studies and clinical applications. These systems offer unique platforms for exploring new therapies and understanding their interactions with human cells and the immune system. Here, we focus on a DDS and a peripheral blood mononuclear cell (PBMC)-engrafted humanized mouse model that we recently developed, and consider some of the key components, challenges, and applications to advance these systems towards better cancer treatment on the basis of a better understanding of the immune response. Our DDS is unique and has a dual function, an anticancer effect and a capacity to fine-tune the immune reaction. The PBL-NOG-hIL-4-Tg mouse system is superior to other available humanized mouse systems for the development of such multifunctional DDSs because it supports the rapid reconstruction of an individual donor's immunity and avoids the onset of graft-versus-host disease.

Indexed as

anticancer drugdrug delivery systemhematopoietic stem cellshumanized mouseimmune systemperipheral blood mononuclear cells

Identifiers

PMID39228913
PMCPMC11368775

What OpenQuestion holds

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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.