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Continuous immunosuppression is required for suppressing immune responses to xenografts in non-human primate brains.
Feng, Su; Zhang, Ting; He, Zhengxiao; Zhang, Wenchang; Chen, Yingying; Yue, Chunmei; Jing, Naihe.
Afiliación
  • Feng S; Guangzhou National Laboratory, Guangzhou, 510005, China.
  • Zhang T; Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200080, China.
  • He Z; National Clinical Research Center for Eye Disease, Shanghai, 200080, China.
  • Zhang W; Shanghai Key Laboratory of Ocular Fundus Diseases, Shanghai, 200080, China.
  • Chen Y; Guangzhou National Laboratory, Guangzhou, 510005, China.
  • Yue C; Guangzhou National Laboratory, Guangzhou, 510005, China.
  • Jing N; Guangzhou National Laboratory, Guangzhou, 510005, China.
Cell Regen ; 13(1): 8, 2024 Apr 07.
Article en En | MEDLINE | ID: mdl-38583099
ABSTRACT
Continuous immunosuppression has been widely used in xenografts into non-human primate brains. However, how immune responses change after transplantation in host brains under continuous immunosuppressive administration and whether immunosuppression can be withdrawn to mitigate side effects remain unclear. Human induced neural stem/progenitor cells (iNPCs) have shown long-term survival and efficient neuronal differentiation in primate brains. Here, we evaluate the immune responses in primate brains triggered by human grafts. The results show that the immune responses, including the evident activation of microglia and the strong infiltration of lymphocytes (both T- and B-cells), are caused by xenografts at 4 months post transplantation (p.t.), but significantly reduced at 8 months p.t. under continuous administration of immunosuppressant Cyclosporin A. However, early immunosuppressant withdrawal at 5 months p.t. results in severe immune responses at 10 months p.t. These results suggest that continuous long-term immunosuppression is required for suppressing immune responses to xenografts in primate brains.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cell Regen Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cell Regen Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China