Evidence map›Paper›PMID 33837066›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2022

Longitudinal Imaging of T Cells and Inflammatory Demyelination in a Preclinical Model of Multiple Sclerosis Using

Caroline Guglielmetti, Jelena Levi, Tony L Huynh, Brice Tiret, Joseph Blecha, Ryan Tang, Henry VanBrocklin, Myriam M Chaumeil

Open access · hybridAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  6. A Feasibility Study of [Molecular imaging and biology · 2024
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  15. Fluorinated carbohydrates forChemical Society reviews · 2023
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  17. An improved radiosynthesis of [Journal of labelled compounds & radiopharmaceuticals · 2022
    Article
  18. Simplified and accessible [Journal of labelled compounds & radiopharmaceuticals · 2022
    Article
  19. Review
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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

8 authors at 3 institutions in 1 country.

Caroline GuglielmettiDepartment of Physical Therapy and Rehabilitation Science, University of California, San Francisco, San Francisco, California; caroline.guglielmetti@ucsf.edu.
Jelena LeviCellSight Technologies, Inc., San Francisco, California.
Tony L HuynhDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California.
Brice TiretDepartment of Physical Therapy and Rehabilitation Science, University of California, San Francisco, San Francisco, California.
Joseph BlechaDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California.
Ryan TangDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California.
Henry VanBrocklinDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California.
Myriam M ChaumeilDepartment of Physical Therapy and Rehabilitation Science, University of California, San Francisco, San Francisco, California.
University of California, San Francisco · USAmerican Physical Therapy Association · USCellSight Technologies (United States) · US

Funding

MR Metabolic Imaging of Multiple SclerosisR01NS102156 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jeremy William Gordon, Ari J Green · 2017 to 2026
$3.4M
Application of Hyperpolarized 13C Magnetic Resonance Imaging to Detect Target Inhibition of NF-kB Activation and Response in Primary CNS LymphomaR01CA239462 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHAUMEIL, MYRIAM MARIANNE, RUBENSTEIN, JAMES LOUIS · 2019 to 2023
$3.1M
Imaging innate and adaptive immune response in MS using using [18F]F-AraG PET and hyperpolarized 13C MRSIR21AI153749 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHAUMEIL, MYRIAM MARIANNE, GUGLIELMETTI, CAROLINE · 2020 to 2021
$444k
NCI NIH HHS R01 CA239462NIAID NIH HHS R21 AI153749NINDS NIH HHS R01 NS102156
6 · The paper itself

Abstract

Lymphocytes and innate immune cells are key drivers of multiple sclerosis (MS) and are the main target of MS disease-modifying therapies (DMT). Ex vivo analyses of MS lesions have revealed cellular heterogeneity and variable T cell levels, which may have important implications for patient stratification and choice of DMT. Although MRI has proven valuable to monitor DMT efficacy, its lack of specificity for cellular subtypes highlights the need for complementary methods to improve lesion characterization. Here, we evaluated the potential of 2'-deoxy-2'-

Indexed as

Disease Models, AnimalMagnetic Resonance ImagingMultiple SclerosisPositron-Emission TomographyT-LymphocytesAnimalsDemyelinating DiseasesEncephalomyelitis, Autoimmune, ExperimentalFemaleInflammationMiceMice, Inbred C57BL18F-FAraG PET imagingcentral nervous systemMRImultiple sclerosisT cells

Identifiers

PMID33837066
PMCPMC8717198
OpenAlexW3144341904

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.