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Derry C. Roopenian

Researcher at Tufts University

Publications -  211
Citations -  16371

Derry C. Roopenian is an academic researcher from Tufts University. The author has contributed to research in topics: Antigen & Major histocompatibility complex. The author has an hindex of 60, co-authored 206 publications receiving 15087 citations. Previous affiliations of Derry C. Roopenian include Gulf Coast Regional Blood Center & Vanderbilt University.

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FcRn: the neonatal Fc receptor comes of age

TL;DR: The neonatal Fc receptor for IgG (FcRn) has been well characterized in the transfer of passive humoral immunity from a mother to her fetus and throughout life, FcRm protects IgG from degradation, thereby explaining the long half-life of this class of antibody in the serum.
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Regulation of B cell differentiation and plasma cell generation by IL-21, a novel inducer of Blimp-1 and Bcl-6

TL;DR: It is demonstrated that although IL-21 induces death of resting B cells, it promotes differentiation of B cells into postswitch and plasma cells, explaining howIL-21 can be proapoptotic for B cells in vitro yet critical for Ag-specific Ig production in vivo.
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Enhanced antibody half-life improves in vivo activity

TL;DR: It is observed that prolonged exposure due to FcRn-mediated enhancement of half-life improved antitumor activity of Fc-engineered antibodies in an hFc Rn/Rag1−/− mouse model, which bridges the demand for dosing convenience with the clinical necessity of maintaining efficacy.
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The major histocompatibility complex-related Fc receptor for IgG (FcRn) binds albumin and prolongs its lifespan.

TL;DR: These results affirm the hypothesis that the major histocompatibility complex–related Fc receptor protects albumin from degradation just as it does IgG, prolonging the half-lives of both.
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Human Neonatal Fc Receptor Mediates Transport of IgG into Luminal Secretions for Delivery of Antigens to Mucosal Dendritic Cells

TL;DR: It is found that the human neonatal Fc receptor (FcRn) is the vehicle that transports IgG across the intestinal epithelial barrier into the lumen where the IgG can bind cognate antigen.