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Publication : Necrotizing enterocolitis induces T lymphocyte-mediated injury in the developing mammalian brain.

First Author  Zhou Q Year  2021
Journal  Sci Transl Med Volume  13
Issue  575 PubMed ID  33408187
Mgi Jnum  J:300147 Mgi Id  MGI:6491814
Doi  10.1126/scitranslmed.aay6621 Citation  Zhou Q, et al. (2021) Necrotizing enterocolitis induces T lymphocyte-mediated injury in the developing mammalian brain. Sci Transl Med 13(575)
abstractText  Necrotizing enterocolitis (NEC) causes acute intestinal necrosis in premature infants and is associated with severe neurological impairment. In NEC, Toll-like receptor 4 is activated in the intestinal epithelium, and NEC-associated brain injury is characterized by microglial activation and white matter loss through mechanisms that remain unclear. We now show that the brains of mice and humans with NEC contained CD4(+) T lymphocytes that were required for the development of brain injury. Inhibition of T lymphocyte influx into the brains of neonatal mice with NEC reduced inflammation and prevented myelin loss. Adoptive intracerebroventricular delivery of gut T lymphocytes from mice with NEC into Rag1 (-/-) recipient mice lacking CD4(+) T cells resulted in brain injury. Brain organoids derived from mice with or without NEC and from human neuronal progenitor cells revealed that IFN-gamma release by CD4(+) T lymphocytes induced microglial activation and myelin loss in the organoids. IFN-gamma knockdown in CD4(+) T cells derived from mice with NEC abrogated the induction of NEC-associated brain injury after adoptive transfer to naive Rag1 (-/-) recipient mice. T cell receptor sequencing revealed that NEC mouse brain-derived T lymphocytes shared homology with gut T lymphocytes from NEC mice. Intraperitoneal injection of NEC gut-derived CD4(+) T lymphocytes into naive Rag1 (-/-) recipient mice induced brain injury, suggesting that gut-derived T lymphocytes could mediate neuroinflammation in NEC. These findings indicate that NEC-associated brain injury may be induced by gut-derived IFN-gamma-releasing CD4(+) T cells, suggesting that early management of intestinal inflammation in children with NEC could improve neurological outcomes.
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