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Yolanda D. Mahnke

Researcher at Vaccine Research Center

Publications -  33
Citations -  7077

Yolanda D. Mahnke is an academic researcher from Vaccine Research Center. The author has contributed to research in topics: T cell & Cytotoxic T cell. The author has an hindex of 19, co-authored 32 publications receiving 5885 citations. Previous affiliations of Yolanda D. Mahnke include Ludwig Institute for Cancer Research & German Cancer Research Center.

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Chimeric antigen receptor T cells for sustained remissions in leukemia.

TL;DR: Chimeric antigen receptor-modified T-cell therapy against CD19 was effective in treating relapsed and refractory ALL and was associated with a high remission rate, even among patients for whom stem-cell transplantation had failed, and durable remissions up to 24 months were observed.
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The who's who of T-cell differentiation: human memory T-cell subsets.

TL;DR: Recent developments in the characterization of the heterogeneity of the memory T‐cell compartment are reviewed, and a unified classification of both human and nonhuman primate T cells on the basis of phenotypic traits and in vivo properties is proposed.
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Chimeric Antigen Receptor T Cells against CD19 for Multiple Myeloma

TL;DR: A patient with refractory multiple myeloma received an infusion of CTL019 cells, a cellular therapy consisting of autologous T cells transduced with an anti-CD19 chimeric antigen receptor, after myeloablative chemotherapy and autOLOGous stem-cell transplantation, which led to a complete response.
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Bone marrow as a priming site for T-cell responses to blood-borne antigen

TL;DR: It is demonstrated that naive, antigen-specific T cells home to bone marrow, where they can be primed, and highlighted the uniqueness of bone marrow as an organ important for hemato- and lymphopoiesis and for systemic T cell–mediated immunity.
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The Genetic Architecture of the Human Immune System: A Bioresource for Autoimmunity and Disease Pathogenesis

TL;DR: This data set reveals traits associated with loci known to confer autoimmune susceptibility, providing mechanistic hypotheses linking immune traits with the etiology of disease, and establishes a bioresource that links genetic control elements associated with normal immune traits to common autoimmune and infectious diseases.