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In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
The innate immune system and transplantation
Conrad A Farrar1, Jerzy W Kupiec-Weglinski, Steven H Sacks
1MRC Centre for Transplantation, Division of Transplantation Immunology and Mucosal Biology, King's College London School of Medicine at Guy's, King's College and St. Thomas' Hospitals, London SE1 9RT, United Kingdom.
Transplant stress activates the innate immune system via complement and toll-like receptors, leading to graft rejection. Targeting these pathways may improve transplant outcomes.
Area of Science:
- Immunology
- Transplantation Biology
- Inflammation Research
Background:
- The innate immune system responds broadly to non-infectious stressors.
- Transplantation involves thermal and metabolic stresses that activate innate immunity.
- This activation can augment adaptive immunity and lead to graft rejection.
Purpose of the Study:
- To review the role of complement and toll-like receptor (TLR) systems in transplant injury.
- To examine the effector mechanisms mediated by these innate immune pathways.
- To discuss damage-associated molecular patterns (DAMPs) that initiate these responses.
Main Methods:
- Literature review of studies on innate immunity in transplantation.
- Analysis of evidence implicating complement and TLR pathways in graft rejection.
- Synthesis of information on DAMPs and their role in initiating immune responses.
Main Results:
- Complement and TLR systems are central to transplant-related injury pathways.
- These systems mediate potent effector responses contributing to graft rejection.
- DAMPs are key initiators of the inflammatory cascade in transplantation.
Conclusions:
- Complement and TLR pathways represent significant barriers to successful transplantation.
- Understanding these innate immune mechanisms is crucial for developing new therapies.
- Ongoing clinical trials are investigating therapeutic strategies targeting these pathways.
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