Nanotargeted Delivery of Immune Therapeutics in Type 1 Diabetes
| Author | Jung, Sungwook |
| Author | Ben Nasr, Moufida |
| Author | Bahmani, Baharak |
| Author | Usuelli, Vera |
| Author | Zhao, Jing |
| Author | Sabiu, Gianmarco |
| Author | Seelam, Andy Joe |
| Author | Naini, Said Movahedi |
| Author | Balasubramanian, Hari Baskar |
| Author | Park, Youngrong |
| Author | Li, Xiaofei |
| Author | Khalefa, Salma Ayman |
| Author | Kasinath, Vivek |
| Author | Williams, MacKenzie D. |
| Author | Rachid, Ousama |
| Author | Haik, Yousef |
| Author | Tsokos, George C. |
| Author | Wasserfall, Clive H. |
| Author | Atkinson, Mark A. |
| Author | Bromberg, Jonathan S. |
| Author | Tao, Wei |
| Author | Fiorina, Paolo |
| Author | Abdi, Reza |
| Available date | 2023-11-05T06:14:28Z |
| Publication Date | 2023 |
| Publication Name | Advanced Materials |
| Resource | Scopus |
| ISSN | 9359648 |
| Abstract | Immune therapeutics holds great promise in the treatment of type 1 diabetes (T1D). Nonetheless, their progress is hampered by limited efficacy, equipoise, or issues of safety. To address this, a novel and specific nanodelivery platform for T1D that targets high endothelial venules (HEVs) presented in the pancreatic lymph nodes (PLNs) and pancreas is developed. Data indicate that the pancreata of nonobese diabetic (NOD) mice and patients with T1D are unique in their expression of newly formed HEVs. Anti-CD3 mAb is encapsulated in poly(lactic-co-glycolic acid)-poly(ethylene glycol) nanoparticles (NPs), the surfaces of which are conjugated with MECA79 mAb that recognizes HEVs. Targeted delivery of these NPs improves accumulation of anti-CD3 mAb in both the PLNs and pancreata of NOD mice. Treatment of hyperglycemic NOD mice with MECA79-anti-CD3-NPs results in significant reversal of T1D compared to those that are untreated, treated with empty NPs, or provided free anti-CD3. This effect is associated with a significant reduction of T effector cell populations in the PLNs and a decreased production of pro-inflammatory cytokine in the mice treated with MECA79-anti-CD3-NPs. In summary, HEV-targeted therapeutics may be used as a means by which immune therapeutics can be delivered to PLNs and pancreata to suppress autoimmune diabetes effectively. |
| Sponsor | This work was supported in part by the National Institutes of Health (NIH) under award number 1R01AI164475-01A1. This work was made possible by the National Priorities Research Program award (NPRP9-350-3-074) from the Qatar National Research Fund (a member of The Qatar Foundation). This research was performed with the support of the Network for Pancreatic Organ donors with Diabetes (nPOD; RRID:SCR_014641), a collaborative type 1 diabetes research project supported by JDRF (nPOD: 5-SRA-2018-557-Q-R) and The Leona M. & Harry B. Helmsley Charitable Trust (Grant #2018PG-T1D053, G-2108-04793). The content and views expressed are the responsibility of the authors and do not necessarily reflect the official view of nPOD. Organ Procurement Organizations (OPO) partnering with nPOD to provide research resources are listed at https://npod.org/for-partners/npod-partners/. |
| Language | en |
| Publisher | John Wiley and Sons Inc |
| Subject | drug delivery high endothelial venules nanomedicine targeted therapy type 1 diabetes |
| Type | Article |
| Issue Number | 40 |
| Volume Number | 35 |
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Pharmacy Research [1234 items ]