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Updated: Apr 15, 2026

In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
Cellular and molecular targeting for nanotherapeutics in transplantation tolerance
Kelan A Hlavaty1, Xunrong Luo2, Lonnie D Shea3
1Department of Biomedical Engineering, Northwestern University, 2145 Sheridan Rd / E310, Evanston, IL 60208, USA; Simpson Querrey Institute for BioNanoTechnology (SQI), Northwestern University, Chicago, IL 60611, USA.
Abstract:
The induction of donor-specific tolerance to transplanted cells and organs, while preserving immune function as a whole, remains a highly sought after and elusive strategy for overcoming transplant rejection. Tolerance necessitates modulating a diverse array of cell types that recognize and respond to alloantigens, including antigen presenting cells and T lymphocytes. Nanotherapeutic strategies that employ cellular and biomaterial engineering represent an emerging technology geared towards the goal of inducing transplant tolerance. Nanocarriers offer a platform for delivering antigens of interest to specific cell types in order to achieve tolerogenic antigen presentation. Furthermore, the technologies also provide an opportunity for local immunomodulation at the graft site. Nanocarriers delivering a combination of antigens and immunomodulating agents, such as rapamycin, provide a unique technology platform with the potential to enhance outcomes for the induction of transplant tolerance.
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