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1. Multiparametric Immunoimaging Maps Inflammatory Signatures in Murine Myocardial Infarction Models

3. Development of a Stable Peptide–Major Histocompatibility Complex (MHC) via Sortase and Click Chemistry

5. Trained Immunity-Promoting Nanobiologic Therapy Suppresses Tumor Growth and Potentiates Checkpoint Inhibition

9. Anti–CTLA-4 therapy requires an Fc domain for efficacy

10. Direct and Indirect Regulators of Epithelial–Mesenchymal Transition–Mediated Immunosuppression in Breast Carcinomas

11. Multiparametric Immunoimaging Maps Inflammatory Signatures in Murine Myocardial Infarction Models

13. Supplementary Figure S6 from Targeting Cytokine Therapy to the Pancreatic Tumor Microenvironment Using PD-L1–Specific VHHs

15. Data from Targeting Cytokine Therapy to the Pancreatic Tumor Microenvironment Using PD-L1–Specific VHHs

19. Supplementary Figure Legends from Targeting Cytokine Therapy to the Pancreatic Tumor Microenvironment Using PD-L1–Specific VHHs

29. Noninvasive imaging of immune responses

33. Enzymatic Construction of DARPin-Based Targeted Delivery Systems Using Protein Farnesyltransferase and a Capture and Release Strategy

35. Converting an anti-mouse CD4 monoclonal antibody into an scFv PET imaging agent for longitudinal monitoring of CD4(+) T cells

42. Abstract PR010: Potentiating the efficacy of immune checkpoint blockade by targeting the epithelial-to-mesenchymal transition (EMT) in breast carcinomas

44. Direct and Indirect Regulators of Epithelial–Mesenchymal Transition–Mediated Immunosuppression in Breast Carcinomas

45. 623 Immuno-STATs: Leveraging protein engineering to expand and track antigen-specific T cells in vivo

46. 232 The epithelial-to-mesenchymal transition (EMT) contributes to immunosuppression in breast carcinomas and regulates their response to immune checkpoint blockade

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