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Multiple Aspects of Transplant Tolerance – Mechanisms, Strategies, and Barriers
Submission Deadline: September 30, 2018 (Open) Submit Now
Jean Kwun, PhD
Assistant Professor of Surgery, Duke Transplant Center, Department of Surgery, Duke University Medical Center, 207 Research Dr, Jones 362, Durham, NC 27710, USA
E-Mail: [email protected]
Research Interests: heart transplantation, transplant tolerance, humoral tolerance to organ transplants, mechanisms of antibody-mediated rejection (AMR), establishing a conceptual basis that will translate into therapeutic intervention of AMR
About This Topic
The idea of immunological tolerance was developed from seminal works by Ray Owen, Sir F. MacFarlane Burnet, and Sir Peter Medawar in the mid-20th century. These findings drove transplantation research to identify mechanisms of immune tolerance. However, despite partial success, it was unable to stably induce tolerance in immunocompetent recipients. In the special issue, “Multiple Aspects of Transplant Tolerance”, we will provide a forum for presenting mechanisms, strategies, and challenges for promoting tolerance in transplantation. This will include description of cell populations plays a crucial role in tolerance as well as cell-based approaches (Treg, Mreg, DCreg, CD8 Treg, Tr1, and not excluding BM, apoptotic cell-based strategies), identification/validation of clinical tolerance strategy and biomarkers. Finally, we will also cover B cell immunobiology in transplantation and strategies for B cell and plasma cell tolerance. The special issue will also be open to any author, but mainly invited by guest editor. Each submission will be reviewed by at least two reviewers to ensure a very high quality of papers selected for the Special Issue.
Title: Innate Immune Tolerance in Allo-transplantation
Authors: Andrea Carrion-Webster MD, Sunil Joshi DVM PhD, Asha Pillai MD
Title: Cell Based Therapies in Transplant Tolerance
Authors: Byoung Chol Oh, Giorgio Raimondi, Michael Grzelak
Title: Tolerance in Clinical Liver Transplantation
Authors: Daniel Azoulay and Salim Hamdani
Title: Medawar's Paradox and Immune Mechanisms of Fetomaternal Tolerance
Authors: Victoria R. Rendell, MD and Todd V. Brennan, MD MS
Title: Clinical Tolerance induction trials – Where do we stand?
Authors: Antje Habicht, Joachim Andrassy
Title: T Cell Exhaustion: A Novel Mechanism of Transplant Tolerance
Authors: Zubair Ilyas, Mohammed Javeed I Ansari
Title: Antibody-Based Therapies in Transplant Tolerance
Authors: Maite Van Hentenryck, Zhanzhuo Li, Patricia Favaro, Philip Murphy, Agnieszka Czechowicz
Title: Innate Mechanisms of MHC- independent Transplant Tolerance
Authors: Sunil Joshi, Asha Pillai
Title: Induction of tolerance using hematopoietic cell transplantation in large animal models
Authors: Scott S. Graves, Rainer Storb, David Mathes, Bruce Swearingen
Title: Prospects for Tolerance in Vascularized Composite Allotransplantation
Authors: Nicole M. Shockor, Arthur J. Nam, Stephen T. Bartlett, Rolf N. Barth
Affiliation: University of Maryland School of Medicine
Title: PRESENT AND FUTURE STRATEGIES FOR THE TREATMENT OF HEREDITARY HEMOGLOBINOPATHIES
Authors: Vanessa Gonçalves de Oliveira 1, Ana Filipa Saraiva 2, Fátima Costa 2, Aida Botelho de Sousa 2
Affiliations: 1. Transfusion Medicine Unit, Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal;
2. Hematology and Hematopoietic Stem Cell Transplant Unit, Hospital Santo António dos Capuchos, Centro Hospitalar de Lisboa Central (CHLC), Lisbon, Portugal.
Abstract: Nowadays, hematopoietic stem cell transplantation (HSCT) is a common procedure in Hematology Units within Reference Centres, mainly for the treatment of hematological malignancies such as multiple myeloma, lymphoma and acute leukemia. Nevertheless, HSCT has much wider applications namely in autoimmune diseases, congenital metabolic defects and hemoglobinopathies. Thalassemia major and sickle cell disease comprise, altogether, the most frequent hereditary hemoglobinopathies worldwide. Despite the advances on the prevention and treatment of complications related to these diseases, still, the only curative approach available resides in allogeneic HSCT. The main challenges of this treatment remain focused on the toxicity of pre-transplant conditioning regimens and short-term transplant related complications like graft-versus-host disease, infections and disease recurrence. Thus, it is crucial to establish a balance between the risk vs benefit of HSCT for each patient and follow the available guidelines for both diseases. Recently, gene therapy is becoming a real alternative to allogeneic HSCT. Recent advances in molecular biology methods have provided more accurate and reliable gene editing techniques such as the CRISP/CAS9 system. The long-term outcome of gene manipulation procedures remains uncertain, especially in the immune system of the host. This review will focus on HSCT and gene therapy in hereditary hemoglobinopathies.
Title: Potential role of high-dose cyclophosphamide for tolerance in solid organ transplantation
Author: Roberto Crocchiolo
Title: Thymus tissue engineering to induce transplantation tolerance
Author: Yong Fan
Title: Role of regulatory T cell in Transplant Tolerance
Author: Annalisa Paviglianiti
Anouk A. J. Hamers, Sunil K. Joshi, Asha B. Pillai
Received: September 29, 2018; Published: January 31, 2019; doi:10.21926/obm.transplant.1901044
Yi-nan Guo, Michael Grzelak, Byoung Chol Oh
Received: October 10, 2018; Published: December 14, 2018; doi:10.21926/obm.transplant.1804031
Yujie Wen, Anita Y. Chhabra, Joseph R. Leventhal, Suzanne T. Ildstad
Received: October 29, 2018; Published: November 21, 2018; doi:10.21926/obm.transplant.1804027
Sylvaine You, Lucienne Chatenoud
Received: September 25, 2018; Published: November 09, 2018; doi:10.21926/obm.transplant.1804025
Rene J. Duquesnoy
Received: July 11, 2018; Published: September 6, 2018; doi:10.21926/obm.transplant.1803018