Evidence map›Paper›PMID 33725478›Full record

ArticleImmunity2021

Pleiotropic consequences of metabolic stress for the major histocompatibility complex class II molecule antigen processing and presentation machinery.

Cristina C Clement, Padma P Nanaware, Takahiro Yamazaki, Maria Pia Negroni, Karthik Ramesh, Kateryna Morozova, Sangeetha Thangaswamy, Austin Graves, Hei Jung Kim, Tsai Wanxia Li and 9 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 53 citations in OpenAlex.

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  9. Immunometabolism in atherosclerotic disorders.Nature cardiovascular research · 2024
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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

19 authors at 7 institutions in 3 countries.

Cristina C ClementDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA.
Padma P NanawareDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA, USA.
Takahiro YamazakiDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA.
Maria Pia NegroniDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA, USA.
Karthik RameshImmunology and Microbiology Program, University of Massachusetts Medical School, Worcester, MA, USA.
Kateryna MorozovaDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA.
Sangeetha ThangaswamyDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA.
Austin GravesChild Health Institute of New Jersey, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Hei Jung KimExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Tsai Wanxia LiTranslational Immunology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.
Marco Vigano'Orthopedic Biotechnology Lab, Galeazzi Orthopedic Institute for Care and Scientific Research, Milan, Italy.
Rajesh K SoniProteomics and Macromolecular Crystallography Shared Resource, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Massimo GadinaTranslational Immunology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.
Harley Y TseDepartment of Microbiology and Immunology, Cardiovascular Research Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Lorenzo GalluzziDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA; Sandra and Edward Meyer Cancer Center, New York, NY, USA; Caryl and Israel Englander Institute for Precision Medicine, New York, NY, USA.
Paul A RocheExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Lisa K DenzinChild Health Institute of New Jersey, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Lawrence J SternDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA, USA; Immunology and Microbiology Program, University of Massachusetts Medical School, Worcester, MA, USA. Electronic address: lawrence.stern@umassmed.edu.
Laura SantambrogioDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY, USA; Sandra and Edward Meyer Cancer Center, New York, NY, USA; Caryl and Israel Englander Institute for Precision Medicine, New York, NY, USA. Electronic address: las4011@med.cornell.edu.
Cornell University · USNational Institutes of Health · USUniversity of Massachusetts Chan Medical School · USRutgers, The State University of New Jersey · USColumbia University Irving Medical Center · USIstituto Ortopedico Galeazzi · ITWayne State University · US

Funding

Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2009 to 2024
$36.2M
Translational Immunology research: a support for clinical immunological researchZICAR041181 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI GADINA, MASSIMO · 2009 to 2025
$31.5M
Regulation of MHC Class II Trafficking in Antigen Presenting CellsZIABC009404 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROCHE, PAUL · 2009 to 2025
$17.9M
DYNAMICS AND TUNING OF THE MHC II PRESENTED PEPTIDOMER01AI137198 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI SANTAMBROGIO, LAURA, STERN, LAWRENCE J. · 2018 to 2022
$4.6M
Effects of Glycation and Carbonylation on MHC II-restricted immunityR01AI146180 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI SANTAMBROGIO, LAURA, STERN, LAWRENCE J. · 2020 to 2024
$3.7M
New retroviral restriction factorR01AI117535 · NIAID · UNIVERSITY OF CHICAGO · PI GOLOVKINA, TATYANA V · 2016 to 2020
$3.2M
NIAID NIH HHS R01 AI117535NIAID NIH HHS R01 AI137198NIAID NIH HHS R01 AI146180NIA NIH HHS P01 AG031782
6 · The paper itself

Abstract

Hyperglycemia and hyperlipidemia are often observed in individuals with type II diabetes (T2D) and related mouse models. One dysmetabolic biochemical consequence is the non-enzymatic reaction between sugars, lipids, and proteins, favoring protein glycation, glycoxidation, and lipoxidation. Here, we identified oxidative alterations in key components of the major histocompatibility complex (MHC) class II molecule antigen processing and presentation machinery in vivo under conditions of hyperglycemia-induced metabolic stress. These modifications were linked to epitope-specific changes in endosomal processing efficiency, MHC class II-peptide binding, and DM editing activity. Moreover, we observed some quantitative and qualitative changes in the MHC class II immunopeptidome of Ob/Ob mice on a high-fat diet compared with controls, including changes in the presentation of an apolipoprotein B100 peptide associated previously with T2D and metabolic syndrome-related clinical complications. These findings highlight a link between glycation reactions and altered MHC class II antigen presentation that may contribute to T2D complications.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Disease Models, AnimalEpitopesFemaleHistocompatibility Antigens Class IIMaleMiceMice, Inbred C57BLPeptidesProtein BindingStress, PhysiologicalEpitopesHistocompatibility Antigens Class IIPeptidesadvanced glycation end productsantigen processing and presentationCD4(+) T cellsdendritic cellsdiabeteshyperinsulinemiaMHC class IIobesityoxidative posttranslational modifications

Identifiers

PMID33725478
PMCPMC8046741
OpenAlexW3139485039

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.