Dr. Riddha Das
Research Assistant ProfessorOur work brings together nanomedicine, immunoengineering, and biomaterials to control how immune cells behave across different disease settings. We investigate disease-relevant immune pathways and use these insights to design cell-based, nanoscale, and biomaterial-based therapeutic strategies for cancer, autoimmune disorders, and women’s health. Our broader aim is to translate mechanistic discoveries into clinically relevant therapies that improve human health. Major areas of focus include:
- Ex vivo Immune-Cell Engineering and Adoptive Immunotherapy
We develop ex vivo engineered immune-cell platforms for controlled and customizable cell-based therapies. A major focus is on reprogramming antigen-presenting cells, including dendritic cells and macrophages, into therapeutically beneficial ‘phenotypical’ states before administration. These cells coordinate immune responses through antigen presentation, cytokine production, and communication with T cells. Ex vivo engineering enables precise control over cell phenotype and function, reduces reliance on tissue-delivery barriers, and allows therapeutic cells to be characterized before treatment. Through this work, we aim to develop consistent, adaptable cellular therapies tailored to specific disease settings.
- Biomimetic Nanomedicine for Precision Delivery
We are interested in developing biomimetic nanomaterials that leverage the natural targeting and immune-interaction properties of biological systems. Extracellular vesicles, for example, retain surface proteins, lipids, and molecular signatures from their parent cells that can influence tissue localization, cellular recognition, and immune responses. We seek to incorporate these biologically relevant features into engineered delivery platforms while maintaining control over cargo loading, stability, and pharmacokinetics. By tailoring these systems to the molecular and immunological characteristics of specific diseases and patients, our goal is to advance patient-informed precision nanomedicine and immunotherapy.
- Implantable Biomaterials for Localized Immunomodulation
We design implantable biomaterials, including electrospun nanofiber scaffolds, to control immune responses directly at sites of disease or tissue injury. Localized delivery can maintain therapeutic activity where it is needed while reducing systemic exposure and treatment-associated toxicity. These materials will be engineered with tunable degradability, stiffness, and layer-by-layer architectures to incorporate multiple payloads and release them at distinct rates. The resulting scaffolds can also create supportive microenvironments for immune-cell function, cell therapy, and tissue regeneration, providing adaptable platforms for localized treatment.
2025 Massachusetts General Hospital Travel Award
2024 Leadership in Diversity Award by the Immunomodulation and Engineering Symposium
2024 Award for Outstanding Presentation by Society for Biomaterials
2024 Recognition for outstanding research at the MGB Women in Medicine and Science Symposium
2024 RNA Therapeutics Inclusivity Grant
2022 NIH T32 Fellowship
2019 People’s Choice Award in Three Minute Thesis 3MT®, UMass Amherst
2018 Gordon Chair Scholarship
2015 Award for Excellence in Teaching Assistance, UMass Amherst
2011 GATE Scholarship, Ministry of Human Resources Development, Government of India
- Anderson, D.G.; Gupta, A.; Reed, K.P.; Weissleder, R.; Garris, C.; Das, R.; US Patent App. 63/746,840, Filed January 2025, “mRNA-based Myeloid Cell Stimulation Enhances Therapeutic Efficacy”Date: 01/01/2025
Selected Publications
- Gupta, A., Das, R., Reed, K., Jeon, T., Nguyen, Q.T.C., Rudra, A., Ge, X., Trongjit, S., Langer, R., Weissleder, R., Garris, C., and Anderson, D.G., Immune-remodelling mRNAs expressing IRF8 or NIK generate durable anti-tumor immunity in multiple cancer models. Nat. Biotechnol. https://doi.org/10.1038/s41587-026-03115-2, 2026
- Das, R., Ge, X., Fei, F., Weissleder, R., Garris, C. S.,, Lipid Nanoparticle-mRNA Engineered DC Adoptive Cell Therapy Enhances Cancer Immune Response. Small Methods. 2024. https://onlinelibrary.wiley.com/doi/full/10.1002/smtd.202400633, 2024
- Das, R., Halabi, E.A., Fredrich, I.R., Oh, J., Peterson, H.M., Ge, X., Scott, E., Kohler, R., Garris, C.S., Weissleder, R., Hybrid LNP Prime Dendritic Cells for Nucleotide Delivery. Adv. Sci. 2023 https://advanced.onlinelibrary.wiley.com/doi/10.1002/advs.202303576, 2023
- Das, R., Hardie, J., Joshi, B.P., Zhang, X., Gupta, A., Luther, D.C., Fedeli, S., Farkas, E.M., Rotello, V.M.,, Macrophage-Encapsulated Bioorthogonal Nanozymes for Targeting Cancer Cells, JACS Au 2022. https://pubs.acs.org/doi/10.1021/jacsau.2c00247, 2022
- Das, R., Landis, R.F., Yesilbag Tonga, G., Cao-milán, R., Luther, D.C., Rotello, V.M.,, Control of Intra-versus Extracellular Bioorthogonal Catalysis using Surface Engineered Nanozymes, ACS Nano 2019. https://pubs.acs.org/doi/10.1021/acsnano.8b05370, 2019