Evidence map›Paper›PMID 40293219›Full record

ArticleeLife2025

Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system mice.

Mohsen Khosravi-Maharlooei, Andrea Vecchione, Nichole Danzl, Hao Wei Li, Grace Nauman, Rachel Madley, Elizabeth Waffarn, Robert Winchester, Amanda Ruiz, Xiaolan Ding and 2 more

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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  3. Review
  4. Article
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Mohsen Khosravi-MaharlooeiColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.ORCID https://orcid.org/0009-0001-2385-3714
Andrea VecchioneColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.
Nichole DanzlColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.
Hao Wei LiColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.
Grace NaumanColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.
Rachel MadleyColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.
Elizabeth WaffarnColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.
Robert WinchesterColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.ORCID https://orcid.org/0000-0002-7543-8037
Amanda RuizColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.ORCID https://orcid.org/0000-0002-6404-4905
Xiaolan DingColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.ORCID https://orcid.org/0009-0009-5220-1465
Georgia FousteriSan Raffaele Hospital, Milan, Italy.
Megan SykesColumbia Center for Translational Immunology, Department of Medicine, Columbia University Medical Center, Columbia University, New York, United States.ORCID https://orcid.org/0000-0002-4947-4376

Funding

XENOGRAFT TOLERANCE THROUGH MIXED CHIMERISMP01AI045897 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Megan Sykes · 2000 to 2026
$71.9M
Modeling autoimmune pathogenesis and beta cell destruction by T1D immune systemsU01DK123559 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ANDERSON, MARK S, PARENT, AUDREY · 2019 to 2023
$4.3M
NIAID NIH HHS P01 AI045897NIDDK NIH HHS U01 DK123559NIH HHS P01 AI 045897NIH HHS U01 DK 123559
6 · The paper itself

Abstract

Human immune system (HIS) mice constructed in various ways are widely used for investigations of human immune responses to pathogens, transplants, and immunotherapies. In HIS mice that generate T cells de novo from hematopoietic progenitors, T cell-dependent multisystem autoimmune disease occurs, most rapidly when the human T cells develop in the native NOD.Cg-

Indexed as

Autoimmune DiseasesT Follicular Helper CellsT-Lymphocytes, Helper-InducerAnimalsDisease Models, AnimalHumansMiceMice, Inbred NODThymus GlandautoimmunityB cellshuman immune systemimmunologyinflammationmouseT cellsT follicular helper cellT peripheral helper cell

Identifiers

PMID40293219
PMCPMC12037178

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.