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Daniel D. Pinschewer

Researcher at University of Basel

Publications -  100
Citations -  5745

Daniel D. Pinschewer is an academic researcher from University of Basel. The author has contributed to research in topics: Lymphocytic choriomeningitis & Virus. The author has an hindex of 38, co-authored 93 publications receiving 5007 citations. Previous affiliations of Daniel D. Pinschewer include World Health Organization & Scripps Research Institute.

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Interferons Direct Th2 Cell Reprogramming to Generate a Stable GATA-3+T-bet+ Cell Subset with Combined Th2 and Th1 Cell Functions

TL;DR: Functional reprogramming of unfavorably differentiated Th2 cells may facilitate the establishment of protective immune responses and provide a molecular concept for the long-term coexistence of Th2 and Th1 cell lineage characteristics in single memory T cells.
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FTY720 immunosuppression impairs effector T cell peripheral homing without affecting induction, expansion, and memory.

TL;DR: FTY720 effectively reduced recirculation of CD8+ effector T cells and their recruitment to peripheral lesions without affecting the induction and expansion of immune responses in secondary lymphoid organs, and may offer the potential to treat ongoing organ-specific T cell-mediated immunopathologic disease.
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The Alarmin Interleukin-33 Drives Protective Antiviral CD8+ T Cell Responses

TL;DR: It is shown that interleukin-33 (IL-33), an alarmin released from necrotic cells, is necessary for potent CD8+ T cell responses to replicating, prototypic RNA and DNA viruses in mice and showed that endogenous material, independently of pathogen-derived molecules, are also required for antiviral immunity.
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Protective long-term antibody memory by antigen-driven and T help-dependent differentiation of long-lived memory B cells to short-lived plasma cells independent of secondary lymphoid organs

TL;DR: It is suggested that memory B cells are long-lived in the absence of antigen, nondividing, and relatively resistant to irradiation and must be stimulated by antigen to differentiate to short-lived antibody-secreting plasma cells, a process that is also efficient in the bone marrow and always depends on radiosensitive, specific T help.
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FTY720: altered lymphocyte traffic results in allograft protection.

TL;DR: The novel immunomodulator FTY720 protects allografts including islets with remarkable potency, apparently without inducing generalized immunosuppression, and increases the intrinsic mobility of lymphocytes, thereby accelerating chemokine-dependent lymphocyte homing to secondary lymphoid tissues.