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Agnieszka J. Szczepek

Researcher at Humboldt University of Berlin

Publications -  132
Citations -  3154

Agnieszka J. Szczepek is an academic researcher from Humboldt University of Berlin. The author has contributed to research in topics: Tinnitus & Medicine. The author has an hindex of 29, co-authored 112 publications receiving 2649 citations. Previous affiliations of Agnieszka J. Szczepek include Cross Cancer Institute & University of Zielona Góra.

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In multiple myeloma, clonotypic B lymphocytes are detectable among CD19+ peripheral blood cells expressing CD38, CD56, and monotypic Ig light chain [published erratum appears in Blood 1995 Jun 1;85(11):3365]

TL;DR: It is concluded that monoclonal B cells in the blood of myeloma patient populations include drug-resistant reservoirs of clonotypic cells that may underlie relapse.
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A High Frequency of Circulating B Cells Share Clonotypic Ig Heavy-Chain VDJ Rearrangements With Autologous Bone Marrow Plasma Cells in Multiple Myeloma, as Measured by Single-Cell and In Situ Reverse Transcriptase-Polymerase Chain Reaction

TL;DR: Their high frequency in the blood, and their resistence to conventional chemotherapy suggests that the number of circulating clonotypic cells should be clinically monitored, and that therapeutic targeting of these B cells may benefit myeloma patients.
Journal ArticleDOI

In Multiple Myeloma, Clonotypic B Lymphocytes Are Detectable Among CD19+ Peripheral Blood Cells Expressing CD38, CD56, and Monotypic Ig Light Chain

TL;DR: Analysis of CD45 isoform expression on CD19+ cells in the blood and BM of myeloma patients indicates a heterogeneous continuously differentiating B lineage in contrast to other Bcell malignancies such as B-cell chronic lymphocytic leukemia (B-CLL), lymphoma, or hairy cell le~kemia.
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CD20-directed serotherapy in patients with multiple myeloma: biologic considerations and therapeutic applications.

TL;DR: It is suggested that multiple myeloma patients with CD20 + BMPCs may benefit from rituximab therapy, and the rationale for clinical trials to examine its use withCD20-directed serotherapies in MM is examined.