Evidence map›Paper›PMID 38848214›Full record

ArticleCell reports2024

Role of the afferent lymph as an immunological conduit to analyze tissue antigenic and inflammatory load.

Padma P Nanaware, Zohaib N Khan, Cristina C Clement, Madhur Shetty, Ines Mota, Ethan S Seltzer, Monika Dzieciatkowska, Fabia Gamboni, Angelo D'Alessandro, Charles Ng and 12 more

Abstract read
In one paragraph

Article in Cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Lung Lymphatics in Edema, Inflammation, and Thrombosis.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

22 authors.

Padma P NanawareDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065, USA; Department of Pathology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Zohaib N KhanDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065, USA.
Cristina C ClementDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065, USA.
Madhur ShettyDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065, USA.
Ines MotaDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065, USA.
Ethan S SeltzerPediatric Rheumatology and Autoimmunity and Inflammation Program, Hospital for Special Surgery Research Institute, New York NY 100021, USA.
Monika DzieciatkowskaDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Fabia GamboniDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Angelo D'AlessandroDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Charles NgDepartment of Pathology and Laboratory Medicine, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, NY 10065, USA.
Manabu NagayamaDivision of Gastroenterology and Hepatology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, NY 10065, USA.
Cheryl F LichtiDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Rajesh K SoniProteomics and Macromolecular Crystallography Shared Resource, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York 10032, NY, USA.
Jacob B GeriChildren's Cancer and Blood Foundation Laboratories, Departments of Pediatrics and Cell and Developmental Biology, Drukier Institute for Children's Health, Weill Cornell Medicine, New York, NY 10065, USA.
Irina MateiChildren's Cancer and Blood Foundation Laboratories, Departments of Pediatrics and Cell and Developmental Biology, Drukier Institute for Children's Health, Weill Cornell Medicine, New York, NY 10065, USA; Sandra and Edward Meyer Cancer Center, New York, NY 10065, USA.
David LydenChildren's Cancer and Blood Foundation Laboratories, Departments of Pediatrics and Cell and Developmental Biology, Drukier Institute for Children's Health, Weill Cornell Medicine, New York, NY 10065, USA; Sandra and Edward Meyer Cancer Center, New York, NY 10065, USA.
Randy LongmanDivision of Gastroenterology and Hepatology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, NY 10065, USA.
Theresa T LuPediatric Rheumatology and Autoimmunity and Inflammation Program, Hospital for Special Surgery Research Institute, New York NY 100021, USA.
Xiaoxiao WanDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Emil R UnanueDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Lawrence J SternDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Laura SantambrogioDepartment of Radiation Oncology, Weill Cornell Medicine, New York, NY 10065, USA; Sandra and Edward Meyer Cancer Center, New York, NY 10065, USA; Caryl and Israel Englander Institute for Precision Medicine, New York, NY 10065, USA. Electronic address: las4011@med.cornell.edu.

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
P50-Admin Core-Harris/GarbP50AR080593 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI John E Harris · 2022 to 2026
$9.2M
Vascular-stromal function and regulation in immunityR01AI079178 · NIAID · HOSPITAL FOR SPECIAL SURGERY · PI Theresa T. Lu · 2010 to 2026
$6.6M
Tick Saliva and Pathogen TransmissionR01AI134696 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Joao Pedra · 2018 to 2026
$5.1M
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
Microglia antigen presentation in the CNS of Alzheimer's diseaseR01AG067581 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BRADSHAW, ELIZABETH M, ELYAMAN, WASSIM · 2020 to 2024
$3.7M
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
Robust workflow software for MRI tracking of glymphatic-lymphatic couplingR01AT011419 · NCCIH · YALE UNIVERSITY · PI BENVENISTE, HELENE D, KIPNIS, JONATHAN · 2021 to 2025
$3.6M
TCR signaling control of thymic Treg selection and immune homeostasisR01AI143976 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BERG, LESLIE JOAN, HUSEBY, ERIC S · 2020 to 2024
$2.9M
Biochemical and functional characterization of a novel anti-inflammatory biogenic amineR01AI169723 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI LAURA SANTAMBROGIO · 2023 to 2026
$2.9M
HLA-DO / H2-O: modulation of MHC-II peptide diversity and Treg population controlR01AI127869 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 2018 to 2022
$2.7M
Mobilizing TAP-independent CD8 T cells through non-canonical cross-presentationR01AI170897 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI Julie Magarian Blander · 2023 to 2026
$2.7M
NCCIH NIH HHS R01 AT011419NIAID NIH HHS R01 AI079178NIAID NIH HHS R01 AI127869NIAID NIH HHS R01 AI134696NIAID NIH HHS R01 AI137198NIAID NIH HHS R01 AI143976NIAID NIH HHS R01 AI146180NIAID NIH HHS R01 AI153828NIAID NIH HHS R01 AI169723NIAID NIH HHS R01 AI170897NIAMS NIH HHS P50 AR080593NIAMS NIH HHS R21 AR081493NIA NIH HHS P01 AG031782NIA NIH HHS R01 AG067581
6 · The paper itself

Abstract

The lymphatic fluid is the conduit by which part of the tissue "omics" is transported to the draining lymph node for immunosurveillance. Following cannulation of the pre-nodal cervical and mesenteric afferent lymphatics, herein we investigate the lymph proteomic composition, uncovering that its composition varies according to the tissue of origin. Tissue specificity is also reflected in the dendritic cell-major histocompatibility complex class II-eluted immunopeptidome harvested from the cervical and mesenteric nodes. Following inflammatory disruption of the gut barrier, the lymph antigenic and inflammatory loads are analyzed in both mice and subjects with inflammatory bowel diseases. Gastrointestinal tissue damage reflects the lymph inflammatory and damage-associated molecular pattern signatures, microbiome-derived by-products, and immunomodulatory molecules, including metabolites of the gut-brain axis, mapped in the afferent mesenteric lymph. Our data point to the relevance of the lymphatic fluid to probe the tissue-specific antigenic and inflammatory load transported to the draining lymph node for immunosurveillance.

Indexed as

AntigensInflammationLymphLymph NodesMice, Inbred C57BLAnimalsDendritic CellsFemaleHumansInflammatory Bowel DiseasesMaleMiceAntigensantigen presentationantigen processingCP: ImmunologyCrohn's diseaseimmunosurveillanceinflammationlymphlymphaticsMHC immunopeptidomeMHC molecules

Identifiers

PMID38848214
PMCPMC11233987

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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.