Evidence map›Paper›PMID 40629698›Full record

ArticleAnnals of clinical and translational neurology2025

In Vitro Modeling of Natural Killer Cell Cytotoxicity to Inform Personalized ALS Therapeutics.

Benjamin J Murdock, Jihyun Park, Dae-Gyu Jang, Bangyao Zhao, Samuel J Teener, Ian F Webber-Davis, Lili Zhao, Eva L Feldman, Stephen A Goutman

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

9 authors.

Benjamin J MurdockDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-3543-4007
Jihyun ParkDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
Dae-Gyu JangDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0009-0009-7966-1322
Bangyao ZhaoDepartment of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
Samuel J TeenerDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
Ian F Webber-DavisDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
Lili ZhaoDepartment of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
Eva L FeldmanDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-9162-2694
Stephen A GoutmanDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0001-8780-6637

Funding

Developing novel strategies for personalized treatment and prevention of ALS: Leveraging the global exposome, genome, epigenome, metabolome, and inflammasome with data science in a case/control cohortR01NS127188 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BATTERMAN, STUART A, FELDMAN, EVA LUCILLE · 2021 to 2024
$3.4M
Creating a foundation for personalized age- and sex-based immune-targeted therapies from an ALS longitudinal cohort by identifying peripheral and central immune signaturesR01NS120926 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GOUTMAN, STEPHEN, MURDOCK, BENJAMIN JOSEPH · 2021 to 2025
$3.0M
ACL HHS R01TS000339ALS Association 20-IIA-431ATSDR CDC HHS R01 TS000339Coleman Discovery FundHiller and Novak FamiliesNeuroNetwork for Emerging Therapies at the University of MichiganNIH HHS R01NS120926NIH HHS R01NS127188NINDS NIH HHS R01 NS120926NINDS NIH HHS R01 NS127188Peter R. Clark Fund for ALS ResearchRobert A. Epstein and Joan M. Chernoff-Epstein Emerging Scholar FundScott L. PrangerSinai Medical Staff FoundationU.S. Department of Defense AL200064
6 · The paper itself

Abstract

objectiveNatural killer (NK) cells might contribute to motor neuron death in amyotrophic lateral sclerosis (ALS) through direct cytotoxicity, a process that could be inhibited with the FDA-approved JAK/STAT pathway inhibitor, tofacitinib. This study aimed to verify that tofacitinib can suppress NK cell cytotoxicity, investigate if immune cell profiles can predict responsiveness to tofacitinib, and assess the role of NK cell cytotoxicity in ALS progression.

methodsPrimary NK cells were isolated from peripheral blood samples of ALS participants and healthy controls. NK cells were then co-cultured with target cancer cells, with or without tofacitinib, to assess their cytotoxic activity. Flow cytometry was used to generate immune profiles for each participant, based on 154 immune markers, to explore correlations with NK cell cytotoxicity and response to tofacitinib. The potential association between NK cell cytotoxicity and disease severity, as measured by the revised ALS Functional Rating Scale, was also assessed. All analyses were stratified by age and sex.

resultsTofacitinib effectively reduced the cytotoxicity of primary NK cells isolated from the blood of ALS participants (n = 80) and healthy controls (n = 71), with immune cell profiles correlating with the response to tofacitinib. However, NK cell cytotoxicity was lower in ALS participants compared to healthy controls and showed no association with ALS progression.

interpretationThese findings confirm that tofacitinib suppresses NK cell cytotoxicity, and that immune profiling may help identify treatment responder groups. However, further research is needed to fully understand the role and timing of NK cell activity in ALS pathogenesis.

Indexed as

Amyotrophic Lateral SclerosisCytotoxicity, ImmunologicKiller Cells, NaturalPiperidinesProtein Kinase InhibitorsPyrimidinesAdultAgedFemaleHumansMaleMiddle AgedPrecision MedicinePiperidinesProtein Kinase InhibitorsPyrimidinestofacitinibamyotrophic lateral sclerosiscytotoxicityimmune profilesnatural killer cellstofacitinib

Identifiers

PMID40629698
PMCPMC12516253

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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.