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Memory T cells in organ transplantation: progress and challenges
Jaclyn R Espinosa1, Kannan P Samy2, Allan D Kirk2
1Emory University School of Medicine, Department of Surgery, 101 Woodruff Circle, #5101-WMB, Atlanta, Georgia 30322, USA.
Nature Reviews. Nephrology
|March 1, 2016
Summary
Memory T cells mount rapid recall responses and can cause alloimmunity, posing a challenge for organ transplant acceptance. Targeting adhesion molecules on memory T cells may overcome limitations of current immunotherapies.
Area of Science:
- Immunology
- Transplantation immunology
Background:
- Antigen-experienced T cells (memory T cells) differ from naive T cells.
- Memory T cells provide rapid recall responses and can cross-react with similar antigens, leading to alloimmunity.
- Alloimmunity poses a significant barrier to successful allograft acceptance.
Purpose of the Study:
- To review current immunotherapeutic strategies for controlling memory T-cell responses to allografts.
- To explore novel approaches targeting memory T cells for improved allograft acceptance.
Main Methods:
- Review of existing literature on memory T-cell immunology and allograft acceptance.
- Analysis of current and potential immunotherapeutic interventions.
Main Results:
- Calcineurin inhibition controls memory T cells but increases infection risk.
- Lymphocyte depletion reduces allospecific T cells but spares memory T cells.
- Co-stimulation blockade has a better safety profile but is less effective against memory T cells.
Conclusions:
- Current therapies for allograft acceptance have limitations in controlling memory T cells.
- Targeting adhesion molecules on memory T cells presents a promising strategy to overcome resistance to co-stimulation blockade and improve allograft outcomes.
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