Evidence map›Paper›PMID 41273641›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Preparation of Lentiviral Vectors for the Generation of Transgenic Cynomolgus Monkeys.

Masanaga Muto, Masatsugu Ema

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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
0cells of the map it votes in
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

2 authors.

Masanaga MutoDepartment of Stem Cells and Human Disease Models, Research Center for Animal Life Science, Shiga University of Medical Science, Seta, Tsukinowa-cho, Otsu, Shiga, Japan. mmuto@belle.shiga-med.ac.jp.
Masatsugu EmaDepartment of Stem Cells and Human Disease Models, Research Center for Animal Life Science, Shiga University of Medical Science, Seta, Tsukinowa-cho, Otsu, Shiga, Japan. mema@bella.shiga-med.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonhuman primates (NHPs) are invaluable for modeling human diseases because of their high physiological and genetic similarity to humans. Lentiviral vectors, which offer significant advantages in terms of gene delivery and stable in vivo expression, are widely used to generate transgenic NHP models. The protocol detailed herein provides a comprehensive method for preparing lentiviral vectors for the generation of transgenic cynomolgus monkeys. We describe the procedures for packaging lentiviral vectors, including the transfection and enrichment of lentiviral particles. To optimize lentiviral production and ensure high-titer viral preparations, we utilized Sendai virus hemagglutinin-neuraminidase glycoproteins to enhance infection efficiency. This protocol is designed to support the production of high-quality lentiviral vectors, which are essential for achieving robust, uniform transgene expression in transgenic cynomolgus monkeys to advance human disease modeling and therapeutic research.

Indexed as

Animals, Genetically ModifiedGenetic VectorsLentivirusMacaca fascicularisAnimalsHEK293 CellsHumansTransfectionTransgenesCynomolgus monkeyLentiviral vectorPseudotypingSendai virus hemagglutinin-neuraminidaseTransgenic animal

Identifiers

PMID41273641

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.