Chronic Rejection of Cardiac Allografts Is Associated With Increased Lymphatic Flow and Cellular Trafficking

Lindsey A. Edwards, Anna K. Nowocin, Nazila Jafari, Lucy L. Meader, Kathryn Brown, Aurélien Sarde, Carolyn Lam, Alex Murray and Wilson Wong 2017. Chronic Rejection of Cardiac Allografts Is Associated With Increased Lymphatic Flow and Cellular Trafficking. Circulation. 137, pp. 488-503. https://doi.org/10.1161/circulationaha.117.028533

TitleChronic Rejection of Cardiac Allografts Is Associated With Increased Lymphatic Flow and Cellular Trafficking
TypeJournal article
AuthorsLindsey A. Edwards, Anna K. Nowocin, Nazila Jafari, Lucy L. Meader, Kathryn Brown, Aurélien Sarde, Carolyn Lam, Alex Murray and Wilson Wong
Abstract

Background:
Cardiac transplantation is an excellent treatment for end-stage heart disease. However, rejection of the donor graft, in particular, by chronic rejection leading to cardiac allograft vasculopathy, remains a major cause of graft loss. The lymphatic system plays a crucial role in the alloimmune response, facilitating trafficking of antigen-presenting cells to draining lymph nodes. The encounter of antigen-presenting cells with T lymphocytes in secondary lymphoid organs is essential for the initiation of alloimmunity. Donor lymphatic vessels are not anastomosed to that of the recipient during transplantation. The pathophysiology of lymphatic disruption is unknown, and whether this disruption enhances or hinders the alloimmune responses is unclear. Although histological analysis of lymphatic vessels in donor grafts can yield information on the structure of the lymphatics, the function following cardiac transplantation is poorly understood.

Methods:
Using single-photon emission computed tomography/computed tomography lymphoscintigraphy, we quantified the lymphatic flow index following heterotrophic cardiac transplantation in a murine model of chronic rejection.

Results:
Ten weeks following transplantation of a minor antigen (HY) sex-mismatched heart graft, the lymphatic flow index was significantly increased in comparison with sex-matched controls. Furthermore, the enhanced lymphatic flow index correlated with an increase in donor cells in the mediastinal draining lymph nodes; increased lymphatic vessel area; and graft infiltration of CD4+, CD8+ T cells, and CD68+ macrophages.

Conclusions:
Chronic rejection results in increased lymphatic flow from the donor graft to draining lymph nodes, which may be a factor in promoting cellular trafficking, alloimmunity, and cardiac allograft vasculopathy.

JournalCirculation
Journal citation137, pp. 488-503
ISSN0009-7322
1524-4539
Year2017
PublisherAmerican Heart Association
Digital Object Identifier (DOI)https://doi.org/10.1161/circulationaha.117.028533
Web address (URL)http://dx.doi.org/10.1161/circulationaha.117.028533
Publication dates
Published30 Jan 2018
Published online03 Aug 2017

Related outputs

An immunoresponsive three-dimensional urine-tolerant human urothelial (3D-UHU) model to study urinary tract infection
Nazila V. Jafari and Jennifer L. Rohn 2023. An immunoresponsive three-dimensional urine-tolerant human urothelial (3D-UHU) model to study urinary tract infection. Frontiers in Cellular and Infection Microbiology. https://doi.org/10.3389/fcimb.2023.1128132

Severe Acute Respiratory Syndrome Type 2‐Causing Coronavirus: Variants and Preventive Strategies
Mehmet Onur Aydogdu, Jennifer L. Rohn, Nazila V. Jafari, Francis Brako, Shervanthi Homer‐Vanniasinkam and Mohan Edirisinghe 2022. Severe Acute Respiratory Syndrome Type 2‐Causing Coronavirus: Variants and Preventive Strategies. Advanced Science. 9 (11) 2104495. https://doi.org/10.1002/advs.202104495

The urothelium: a multi-faceted barrier against a harsh environment
Nazila V. Jafari and Jennifer L. Rohn 2022. The urothelium: a multi-faceted barrier against a harsh environment. Mucosal Immunology. 15 (6), pp. 1127-1142. https://doi.org/10.1038/s41385-022-00565-0

Novel antibiotic-loaded particles conferring eradication of deep tissue bacterial reservoirs for the treatment of chronic urinary tract infection
Wai K. Lau, Dhanuson Dharmasena, Harry Horsley, Nazila Jafari, James Malone-Lee, Eleanor Stride, Mohan Edirisinghe and Jennifer L. Rohn 2020. Novel antibiotic-loaded particles conferring eradication of deep tissue bacterial reservoirs for the treatment of chronic urinary tract infection. Journal of Controlled Release. 328, pp. 490-502. https://doi.org/10.1016/j.jconrel.2020.08.048

Effect of Environment on the Evolutionary Trajectories and Growth Characteristics of Antibiotic-Resistant Escherichia coli Mutants
Alasdair T. M. Hubbard, Nazila Jafari, Nicholas Feasey, Jennifer L. Rohn and Adam P. Roberts 2019. Effect of Environment on the Evolutionary Trajectories and Growth Characteristics of Antibiotic-Resistant Escherichia coli Mutants. Frontiers in Microbiology. 10 2001. https://doi.org/10.3389/fmicb.2019.02001

Clostridium difficile-mediated effects on human intestinal epithelia: Modelling host-pathogen interactions in a vertical diffusion chamber
Nazila Jafari, Sarah A. Kuehne, Nigel P. Minton, Elaine Allan and Mona Bajaj-Elliott 2016. Clostridium difficile-mediated effects on human intestinal epithelia: Modelling host-pathogen interactions in a vertical diffusion chamber. Anaerobe. https://doi.org/10.1016/j.anaerobe.2015.12.007

Host Immunity to Clostridium difficile PCR Ribotype 017 Strains
Jafari, N., Mario Songane, Richard A. Stabler, Mamoun Elawad, Brendan W. Wren, Elaine Allan and Mona Bajaj-Elliott 2014. Host Immunity to Clostridium difficile PCR Ribotype 017 Strains. Infection and Immunity. 82 (12), pp. 4989-4996. https://doi.org/10.1128/iai.02605-14

Clostridium difficile modulates host innate immunity via toxin-independent and dependent mechanism(s)
Nazila Jafari, Sarah A. Kuehne, Clare E. Bryant, Mamoun Elawad, Brendan W. Wren, Nigel P. Minton, Elaine Allan and Mona Bajaj-Elliott 2013. Clostridium difficile modulates host innate immunity via toxin-independent and dependent mechanism(s). PLoS ONE. 8 (7) e69846. https://doi.org/10.1371/journal.pone.0069846

Human Intestinal Epithelial Response(s) to Clostridium difficile
Jafari, N., Allan, E. and Bajaj-Elliott, M. 2010. Human Intestinal Epithelial Response(s) to Clostridium difficile. in: Mullany, P. and Roberts, A.P. (ed.) Clostridium difficile Methods and Protocols Humana Totowa. pp. 135-146

Permalink - https://westminsterresearch.westminster.ac.uk/item/w85vz/chronic-rejection-of-cardiac-allografts-is-associated-with-increased-lymphatic-flow-and-cellular-trafficking


Share this

Usage statistics

6 total views
0 total downloads
These values cover views and downloads from WestminsterResearch and are for the period from September 2nd 2018, when this repository was created.