» Articles » PMID: 38848214

Role of the Afferent Lymph As an Immunological Conduit to Analyze Tissue Antigenic and Inflammatory Load

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.

Citing Articles

Lymphatic messengers: Non-antigen soluble mediators from diseased tissues to draining lymph nodes.

Howlader M, Rashighi M, Santambrogio L, Lu T Curr Opin Immunol. 2025; 93:102536.

PMID: 39914124 PMC: 11885046. DOI: 10.1016/j.coi.2025.102536.


Multi-site Ultrasound-guided Fine Needle Aspiration to Study Cells and Soluble Factors From Human Lymph Nodes.

Al-Diwani A, Agrawal D, Sheerin F, Board C, Irani S, Pollock K Curr Protoc. 2024; 4(11):e70063.

PMID: 39579041 PMC: 11585077. DOI: 10.1002/cpz1.70063.


Neurodegenerative fluid biomarkers are enriched in human cervical lymph nodes.

Al-Diwani A, Provine N, Murchison A, Laban R, Swann O, Koychev I Brain. 2024; 148(2):394-400.

PMID: 39432679 PMC: 11788199. DOI: 10.1093/brain/awae329.

References
1.
Hasko G, Kuhel D, Nemeth Z, Mabley J, Stachlewitz R, Virag L . Inosine inhibits inflammatory cytokine production by a posttranscriptional mechanism and protects against endotoxin-induced shock. J Immunol. 2000; 164(2):1013-9. DOI: 10.4049/jimmunol.164.2.1013. View

2.
Seitzer P, Searle B . Incorporating In-Source Fragment Information Improves Metabolite Identification Accuracy in Untargeted LC-MS Data Sets. J Proteome Res. 2018; 18(2):791-796. DOI: 10.1021/acs.jproteome.8b00601. View

3.
Clement C, Cannizzo E, Nastke M, Sahu R, Olszewski W, Miller N . An expanded self-antigen peptidome is carried by the human lymph as compared to the plasma. PLoS One. 2010; 5(3):e9863. PMC: 2845622. DOI: 10.1371/journal.pone.0009863. View

4.
Clement C, Osan J, Buque A, Nanaware P, Chang Y, Perino G . PDIA3 epitope-driven immune autoreactivity contributes to hepatic damage in type 2 diabetes. Sci Immunol. 2022; 7(74):eabl3795. PMC: 9762167. DOI: 10.1126/sciimmunol.abl3795. View

5.
Dzieciatkowska M, Wohlauer M, Moore E, Damle S, Peltz E, Campsen J . Proteomic analysis of human mesenteric lymph. Shock. 2010; 35(4):331-8. PMC: 3059368. DOI: 10.1097/SHK.0b013e318206f654. View