Evidence map›Paper›PMID 40632850›Full record

ArticleScience advances2025

Establishment of a reverse genetics system for studying human immune functions in mice.

Priya Pal, Shuai Gao, Hongbo Gao, Xiwen Qin, Marina Cella, Qiankun Wang, Liang Shan

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Priya PalDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0002-0669-7385
Shuai GaoDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-3338-2431
Hongbo GaoDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Xiwen QinDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Marina CellaDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-1230-1313
Qiankun WangDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0002-4390-4785
Liang ShanDivision of Infectious Diseases, Department of Medicine, Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0002-8833-2514

Funding

CRISPR for CureUM1AI164568 · NIAID · TEMPLE UNIV OF THE COMMONWEALTH · PI Tricia Helen Burdo, Kamel Khalili · 2021 to 2026
$27.7M
Understand the role of CARD8 inflammasome in HIV-1 infectionR01AI162203 · NIAID · WASHINGTON UNIVERSITY · PI PINZONE, MARILIA RITA · 2021 to 2025
$3.5M
Harnessing the CARD8 Inflammasome for HIV Reservoir EliminationR01AI176594 · NIAID · WASHINGTON UNIVERSITY · PI Marilia Rita Pinzone, Francesco Roberto Simonetti · 2023 to 2026
$3.2M
Novel Strategies to Enhance Effector Cell Functions for Antibody-Mediated Clearance of HIV-1 InfectionR01AI155162 · NIAID · WASHINGTON UNIVERSITY · PI SHAN, LIANG · 2020 to 2024
$3.1M
Understanding the mechanism of tropism specific immune restriction in HIV infectionK08AI184158 · NIAID · WASHINGTON UNIVERSITY · PI Priya Pal · 2025 to 2026
$395k
NIAID NIH HHS K08 AI184158NIAID NIH HHS R01 AI155162NIAID NIH HHS R01 AI162203NIAID NIH HHS R01 AI176594NIAID NIH HHS UM1 AI164568
6 · The paper itself

Abstract

Reverse genetics approaches in mice are widely used to understand gene functions and their aberrations in diseases. However, limitations exist in translating findings from animal models to human physiology. Humanized mice provide a powerful bridge to understanding human physiology and mechanisms of disease pathogenesis while maintaining the feasibility of working with small animals. Methods for generating humanized mouse models that allow scientists to probe contributions of particular genes have been rudimentary. Here, we established an efficient method for generating genetically modified human cord blood-derived CD34

Indexed as

Reverse GeneticsAnimalsAntigens, CD34CRISPR-Cas SystemsDisease Models, AnimalFetal BloodGene EditingHumansMiceAntigens, CD34

Identifiers

PMID40632850
PMCPMC12239966

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.