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Henrik E. Mei

Researcher at Leibniz Association

Publications -  77
Citations -  7451

Henrik E. Mei is an academic researcher from Leibniz Association. The author has contributed to research in topics: Mass cytometry & Immune system. The author has an hindex of 32, co-authored 70 publications receiving 5115 citations. Previous affiliations of Henrik E. Mei include Humboldt State University & Stanford University.

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Journal ArticleDOI

Platinum‐conjugated antibodies for application in mass cytometry

TL;DR: Cisplatin‐labeling of antibody increases the analytical capacity of the CyTOF® platform by two channels based on available reagents, and has the potential to add a total of six channels for detection of specific probes, thus helping to better extend the analytical mass range of mass cytometers.
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Steady-state generation of mucosal IgA+ plasmablasts is not abrogated by B-cell depletion therapy with rituximab.

TL;DR: It is demonstrated that recently activated presumably short-lived plasmablasts expressing HLA-DR(high) and Ki-67 continuously circulate in peripheral blood after B-cell depletion by rituximab at 26%-119% of their initial numbers, suggesting that a population of mucosal B cells is self-sufficient in adult humans and not replenished by CD20(+) B cells immigrating from blood, lymphoid tissue, or bone marrow.
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Complement activation induces excessive T cell cytotoxicity in severe COVID-19

TL;DR: The proportion of activated CD16+ T cells and plasma levels of complement proteins upstream of C3a correlated with clinical outcome, supporting a pathological role of exacerbated cytotoxicity and complement activation in COVID-19.
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Secondary Immunization Generates Clonally Related Antigen-Specific Plasma Cells and Memory B Cells

TL;DR: The data indicate that although following secondary immunization PCs can derive from memory B cells without further somatic hypermutation, in some circumstances, likely within GC reactions, asymmetric mutation can occur.
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Rationale of anti-CD19 immunotherapy: an option to target autoreactive plasma cells in autoimmunity

TL;DR: Current known distinct expression profiles of CD19 by human plasma cell subsets, experiences with anti-CD19 therapies in malignant conditions as well as the rationale of targeting autoreactive plasma cells in patients with SLE are discussed in this review.