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Developing a pro-regenerative biomaterial scaffold microenvironment requires T helper 2 cells
Author(s) -
Kaitlyn Sadtler,
Kenneth Estrellas,
Brian W. Allen,
Matthew T. Wolf,
Hongni Fan,
Ada Tam,
Chirag H. Patel,
Brandon Luber,
Hao Wang,
Kathryn R. Wagner,
Jonathan D. Powell,
Franck Housseau,
Drew M. Pardoll,
Jennifer H. Elisseeff
Publication year - 2016
Publication title -
science
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aad9272
Subject(s) - scaffold , biomaterial , microbiology and biotechnology , chemistry , biology , engineering , biomedical engineering , organic chemistry
Immune-mediated tissue regeneration driven by a biomaterial scaffold is emerging as an innovative regenerative strategy to repair damaged tissues. We investigated how biomaterial scaffolds shape the immune microenvironment in traumatic muscle wounds to improve tissue regeneration. The scaffolds induced a pro-regenerative response, characterized by an mTOR/Rictor-dependent T helper 2 pathway that guides interleukin-4-dependent macrophage polarization, which is critical for functional muscle recovery. Manipulating the adaptive immune system using biomaterials engineering may support the development of therapies that promote both systemic and local pro-regenerative immune responses, ultimately stimulating tissue repair.

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