Long-term post-transplant outcomes remain suboptimal, especially for recipients of deceased donor organs. Building upon previous studies, our preliminary data from a murine heart transplant model implicate peri-transplant complement-mediated ischemia reperfusion (IR) injury and inflammation as a central mediator of increased alloimmunity and late graft failure/dysfunction. In this project we will study the mechanisms and effects of complement activation on IR-associated inflammation (Aim 1) and the mechanisms linking increased IR-induced complement-dependent inflammation to late post-transplant allospecific immunity and outcomes (Aim 2).
These aims will test our central hypothesis that IR-injury induced inflammation is dependent upon recipient mannose binding lectin-dependent complement activation, that inflammation induces greater recipient APC activation/donor antigen acquisition, and that these primed APCs then foster a stronger adaptive anti- donor T cell response leading to graft rejection. The specific findings have the potential to identify novel therapeutic targets that can be translated to human trials to improve transplant outcomes. Environment: Both the Icahn School of Medicine at Mount Sinai and Division of Nephrology are firmly committed to junior faculty career development. Dr. Peter Heeger (mentor) is an established expert in the field of complement immunology and transplant research with a strong record of developing junior faculty into independent researchers. Candidate Training: The primary objective of this application is to support Dr. Nicholas Chun's career development into an independent researcher scientist in the field of complement immunobiology and human disease. Dr. Chun's proposed training activities are in four broad non-mutually exclusive areas: 1) Enhancement of fundamental knowledge (e.g. immunology, complement, and exosome biology); 2) Scientific Communication (e.g. manuscript/grant writing, presentation skills); 3) Practical skills (e.g. statistical analysis, large data set analysis, advanced imaging); 4) Managerial skills (e.g. lab finances, personnel administration). The general approaches and skills outlined during this award will form the basis for future research. !

Public Health Relevance

Transplant outcomes remain suboptimal, especially for recipients of deceased donor organs. Prolonged cold ischemic storage and subsequent reperfusion injury in murine models of heart transplant induces early complement-dependent inflammation and increased late adaptive immunity. Herein we will study the mechanisms linking early complement activation to inflammation, late alloimmunity and graft rejection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08AI135101-03
Application #
9915875
Study Section
Allergy, Immunology, and Transplantation Research Committee (AITC)
Program Officer
Gondre-Lewis, Timothy A
Project Start
2018-05-03
Project End
2023-04-30
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029