About this Research Topic
Cellular therapies have been proposed as promising “live” drugs with formidable tolerance-inducing potential being able to target the anti-donor immune response at different cellular levels and to trigger natural mechanisms of dominant tolerance. Different types of cells and different approaches have been proposed and results from the first clinical trials are emerging. For example, infusion of recipient T regulatory or dendritic cells that have been successfully used in solid organ transplantation. In addition to novel cellular therapies, this Research Topic aims at shedding new light on other emerging treatments which include the use of immune-modulatory treatment of donor organs pre or peri-operatively, with the aim to reduce ischemia-reperfusion injury and its associated inflammatory response, including the use of anti-cytokine therapies in the context of bone marrow transplantation.
The aim of this Research Topics is to gather the latest insights on cellular and emerging novel therapies for tolerance induction toward solid organ and bone marrow transplantation, highlighting pre-clinical and clinical achievements and hurdles that need to be overcome.
We welcome authors to submit Original Research, Review, Clinical Trial and Case Report articles focusing on, but not limited to, the following subtopics:
1. Hematopoietic stem cells and chimerism induction
2. Natural and donor-graft specific regulatory T cells
3. CAR Tregs
4. Mesenchymal stromal cells
5. Tolerogenic dendritic cells
6. Regulatory macrophages
7. Apoptotic donor cells
8. The role and modulation of tissue-resident passenger leucocytes
9. The use of biologicals or cytokines to modulate rejection and graft-versus-host disease
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.