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Tolerance induction between two different strains of parental mice prevents graft-versus-host disease in haploidentical hematopoietic stem cell transplantation to F1 mice.
Guo, Yixian; Zhang, Lanfang; Wan, Suigui; Sun, Xuejing; Wu, Yongxia; Yu, Xue-Zhong; Xia, Chang-Qing.
Afiliação
  • Guo Y; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People's Republic of China.
  • Zhang L; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People's Republic of China.
  • Wan S; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People's Republic of China.
  • Sun X; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People's Republic of China.
  • Wu Y; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People's Republic of China.
  • Yu XZ; Department of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC 29425, USA.
  • Xia CQ; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People's Republic of China. Electronic address: cqx65@yahoo.com.
Biochem Biophys Res Commun ; 446(4): 1035-41, 2014 Apr 18.
Article em En | MEDLINE | ID: mdl-24661874
ABSTRACT
Haploidentical hematopoietic stem cell transplantation (Haplo-HSCT) has been employed worldwide in recent years and led to favorable outcome in a group of patients who do not have human leukocyte antigen (HLA)-matched donors. However, the high incidence of severe graft-versus-host disease (GVHD) is a major problem for Haplo-HSCT. In the current study, we performed a proof of concept mouse study to test whether induction of allogeneic tolerance between two different parental strains was able to attenuate GVHD in Haplo-HSCT to the F1 mice. We induced alloantigen tolerance in C3H mice (H-2k) using ultraviolet B (UVB) irradiated immature dendritic cells (iDCs) derived from the cultures of Balb/c bone marrow cells. Then, we performed Haplo-HSCT using tolerant C3H mice as donors to F1 mice (C3H×Balb/c). The results demonstrated that this approach markedly reduced GVHD-associated death and significantly prolonged the survival of recipient mice in contrast to the groups with donors (C3H mice) that received infusion of non-UVB-irradiated DCs. Further studies showed that there were enhanced Tregs in the tolerant mice and alloantigen-specific T cell response was skewed to more IL-10-producing T cells, suggesting that these regulatory T cells might have contributed to the attenuation of GVHD. This study suggests that it is a feasible approach to preventing GVHD in Haplo-HSCT in children by pre-induction of alloantigen tolerance between the two parents. This concept may also lead to more opportunities in cell-based immunotherapy for GVHD post Haplo-HSCT.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Dendríticas / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Dendríticas / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article