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GEO help: Mouse over screen elements for information. |
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| Status |
Public on May 13, 2024 |
| Title |
Microneedle-mediated Delivery of Immunomodulators Restores Immune Privilege in Hair Follicles and Reverses Immune-Mediated Alopecia |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
Disorders in the regulatory arm of the adaptive immune system result in autoimmune-mediated diseases. While systemic immunosuppression is the prevailing approach to manage them, it fails to achieve long-lasting remission due to concomitant suppression of the regulatory arm and carries the risk of heightened susceptibility to infections and malignancies. Alopecia Areata is a condition characterized by localized hair loss due to autoimmunity. The accessibility of the skin provides an opportunity for local rather than systemic intervention to avoid broad immunosuppression. We hypothesized that expansion of endogenous regulatory T cells (Tregs) at the site of antigen encounter can restore the immune balance and generate a long-lasting tolerogenic response. We therefore utilized a hydrogel microneedle (MN) patch for delivery of CCL22, a chemoattractant for Tregs, and IL-2, a Treg survival factor to amplify them. In an immune-mediated murine model of alopecia, we showed local bolstering of Treg numbers leading to sustained hair regrowth and attenuation of inflammatory pathways. In a humanized skin transplant mouse model, we confirmed expansion of Tregs within human skin without engendering peripheral immunosuppression. The MN patch offered high-loading capacity and shelf-life stability for prospective clinical translation. By harmonizing immune responses locally, we aspire to reshape the landscape of autoimmune skin disease management.
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| Overall design |
We performed bulk RNA-sequencing of RNA isolated from AA-like skin lesions from three different experimental groups (untreated, treated with empty MNs, and treated with IL-2+CCL22 loaded MNs).
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| Contributor(s) |
Younis N, Puigmal N, El Kurdi A, Badaoui A, Zhang D, Morales C, Saad A, Cruz D, Al Rahy N, Daccache A, Huerta T, Deban C, Halawi A, Choi J, Dosta P, Lian C, Artzi N, Azzi JR |
| Citation(s) |
38638030 |
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| Submission date |
May 13, 2024 |
| Last update date |
May 13, 2024 |
| Contact name |
Jamil R Azzi |
| E-mail(s) |
jazzi@bwh.harvard.edu
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| Organization name |
Brigham and Women's Hospital
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| Department |
Transplantation Research Center
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| Lab |
AzziLab
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| Street address |
221 Longwood ave
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| City |
Boston |
| State/province |
MA |
| ZIP/Postal code |
02115 |
| Country |
USA |
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| Platforms (1) |
| GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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| Samples (9)
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| Relations |
| BioProject |
PRJNA1110999 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE267295_featureCounts.txt.gz |
1.4 Mb |
(ftp)(http) |
TXT |
SRA Run Selector |
| Raw data are available in SRA |
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