4 results match your criteria: "Roseman University of Health Sciences College of Medicine[Affiliation]"

Article Synopsis
  • - Nearly a dozen monoclonal antibodies (mAbs) targeting beta-amyloid (Aβ) are in development for Alzheimer's disease, with lecanemab showing promise in clinical trials by specifically targeting large Aβ protofibrils.
  • - Phase 2 trials of lecanemab indicated effective results and manageable risks for amyloid-related imaging abnormalities (ARIAs), leading to its further study in phase 3 trials.
  • - The development of Aβ-targeting mAbs is critical for Alzheimer's treatment, with lessons learned from other mAbs like aducanumab, emphasizing the need to target specific Aβ forms for better efficacy and safety monitoring for ARIAs.
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This article presents an update of the collaborative statement on clerkship directors (CDs), first published in 2003, from the national undergraduate medical education organizations that comprise the Alliance for Clinical Education (ACE). The clerkship director remains an essential leader in the education of medical students on core clinical rotations, and the role of the CD has and continues to evolve. The selection of a CD should be an explicit contract between the CD, their department, and the medical school, with each party fulfilling their obligations to ensure the success of the students, the clerkship and of the CD.

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Lessons can be learned for treating inflammatory diseases such as rheumatoid arthritis (RA) from next generation approaches for development of universal influenza vaccines. Immunomodulation of inflammatory diseases, rather than ablation of cytokine or cellular responses, can address the root cause of the disease and provide potential cure. Like influenza, there are different antigenic 'strains' and inflammatory T cell responses, Th1 or Th17, that drive each person's disease.

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Rheumatoid arthritis (RA) is an autoimmune joint disease maintained by aberrant immune responses involving CD4+ T helper (Th)1 and Th17 cells. In this study, we tested the therapeutic efficacy of Ligand Epitope Antigen Presentation System (LEAPS™) vaccines in two Th1 cell-driven mouse models of RA, cartilage proteoglycan (PG)-induced arthritis (PGIA) and PG G1-domain-induced arthritis (GIA). The immunodominant PG peptide PG70 was attached to a DerG or J immune cell binding peptide, and the DerG-PG70 and J-PG70 LEAPS vaccines were administered to the mice after the onset of PGIA or GIA symptoms.

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