Evidence map›Paper›PMID 41947208›Full record

ArticleLaboratory animal research2026

A novel hairless highly immunodeficient mice model optimized for in vivo imaging.

Kouki Matsuda, Ryusho Kariya, Sawako Fujikawa, Kenji Maeda, Seiji Okada

Abstract read
In one paragraph

Article in Laboratory animal research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Kouki MatsudaDivision of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan.
Ryusho KariyaDivision of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan.
Sawako FujikawaDivision of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan.
Kenji MaedaDivision of Antiviral Therapy, Joint Research Center for Human Retrovirus Infection, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Seiji OkadaDivision of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan. okadas@kumamoto-u.ac.jp.ORCID http://orcid.org/0000-0003-3124-5206

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn vivo imaging is one of the analytical technologies that has been rapidly growing in demand in recent years to non-invasively observe the behavior of molecules such as genes and proteins in vivo and perform quantitative and qualitative analysis. Since the hair blocks and absorbs the fluorescence, Nude and Hairless mice have been used for in vivo imaging. Nude mice have been used for in vivo imaging for a long time; however, more efficient mice are needed for the next generation of imaging.

resultsWe established a novel Hairless Rag2/Jak3 KO mice (Hairless R/J mice) model that exhibits hairlessness and a lack of T, B, and NK cell phenotypes. Hairless R/J mice exhibit thinner skin than that of Nude R/J mice. These mice also showed superior optical properties compared with Nude R/J mice, as demonstrated by green fluorescent beads and the mCherry-expressing human cholangiocarcinoma cell line M213, following subcutaneous transplantation. Furthermore, we show that Ihara cells, a human malignant melanoma cell line, can be used to facilitate live imaging of the growth of transplanted tumors.

conclusionsThis novel mouse model will be a valuable tool for noninvasive tumor monitoring and evaluation of anticancer therapies.

Indexed as

Hairless miceImmunodeficiencyIn vivo imagingTumor engraftment

Identifiers

PMID41947208
PMCPMC13054980

What Socratic 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 Socratic graph.