Humanized Models of Disease (HMD) Core
Overview
The Humanized Models of Disease (HMD) Core provides investigators humanized mouse models to effectively conduct translatable research in biomedicine. Humanized mouse models are particularly suited to the investigation of disease and development of therapeutics. The objective of Core service is to deliver humanized mice to test therapeutic interventions as a pre-clinical model; Wistar humanized mice models derived from CD34+ stem cells; archiving/provision of tumor tissue-generation of patient-derived xenograft mice (PDX mice); and the development of primary organoid (tumor) tissue cultures. Cancer humanized platform development is ongoing for (a) organoid and (b) in vivo PDX studies for tumor types including ovarian, lung, and breast cancer. Please inquire for an updated list of available tumor types in each platform.
Services
- Provision of 12 to 14-week Wistar humanized mice using CD34+ stem cell models
- Provision of melanoma PDX mice using NSG.
- Testing of all mice for levels of reconstitution
- Transfer/invoice if mice have >20% human CD45+ lymphocytes engraftment
- Drafts of “grant friendly” text to describe models, grant budget units to include, and support letters
- Provision of advice on items needed per inclusion of humanized mouse models in NIH proposals
- Provision of 3D Organoid Cultures
Any work related to customized differentiation methods or research use of Wistar humanized mice past 12-14 weeks will require collaboration and is outside the scope of Core services available to investigators not otherwise affiliated with Wistar. Please reach out to learn more as several labs have added humanized mice into their protocols.
Selected Publications
Bispecific antibodies promote natural killer cell-mediated elimination of HIV-1 reservoir cells
Board NL, Yuan Z, Wu F, Moskovljevic M, Ravi M, Sengupta S, Mun SS, Simonetti FR, Lai J, Tebas P, Lynn K, Hoh R, Deeks SG, Siliciano JD, Montaner LJ, Siliciano RF. 2024. Nat Immunol 25:462-470. PMC10907297.
PPP2R1A mutations portend improved survival after cancer immunotherapy.
Dai Y, Knisely A, Yano M, Dang M, Hinchcliff EM, Lee S, Welp A, Chelvanambi M, Lastrapes M, Liu H, Yuan Z, Wang C, Nie H, Jean S, Montaner LJ, Hou J, Patel A, Patel S, Fellman B, Yuan Y, Sun B, Pandurengan RK, Cuentas ERP, Celestino J, Liu Y, Liu J, Hillman RT, Westin SN, Sood AK, Soliman PT, Shafer A, Meyer LA, Gershenson DM, Vining D, Ganeshan D, Lu K, Wargo JA, Peng W, Zhang R, Wang L, Jazaeri AA. 2025. Nature 644:537-546. PMC12350166.
Ex vivo and in vivo HIV-1 latency reversal by “Mukungulu,” a protein kinase C-activating African medicinal plant extract
Richard K, Yuan Z, Tang H-Y, Goldman AR, Kuthu R, Raphane B, Register ET, Sharma P, Ross BN, Morris J, Williams DE, Cheney C, Wu G, Mounzer K, Laird GM, Zuck P, Andersen RJ, Simonambango S, Andrae-Marobela K, Tietjen I, Montaner LJ. 2025. mBio 16:e0381624 PMC12077168.
Targeting the mevalonate pathway suppresses ARID1A-inactivated cancers by promoting pyroptosis
PZhou W, Liu H, Yuan Z, Zundell J, Towers M, Lin J, Lombardi S, Nie H, Murphy B, Yang T, Wang C, Liao L, Goldman AR, Kannan T, Kossenkov AV, Drapkin R, Montaner LJ, Claiborne DT, Zhang N, Wu S, Zhang R. 2023. Cancer Cell 41:740-756.e10. PMC10085864.
Human galectin-9 promotes the expansion of HIV reservoirs in vivo in humanized mice
Yuan Z, Giron LB, Hart C, Gyampoh A, Koshy J, Hong KY, Niki T, Premeaux TA, Ndhlovu LC, Deleage C, Montaner LJ, Abdel-Mohsen M. 2023. AIDS 15;37(4):571-577. PMC9975043.
The Wistar Institute
HMD Facility, Room 315
3601 Spruce Street
Philadelphia, PA 19104
(215) 898-3989
Luis J. Montaner, D.V.M., M.Sc., D.Phil.,
Co-Scientific Director
Dr. Meenhard Herlyn, D.V.M., D.Sc.,
Co-Scientific Director
Dr. Zhe (Roger) Yuan, Ph.D.,
Managing Director