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Updated: May 23, 2026

Tumor Transplantation for Assessing the Dynamics of Tumor-Infiltrating CD8+ T Cells in Mice
Published on: June 12, 2021
T-cell engagers mediate deep cell depletion beyond autoimmunity
Johanna T Kurzhagen1, William Laqua1, Mario Schiffer1
1Department of Medicine 4, Nephrology and Hypertension, University Hospital Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Erlangen, Germany; Deutsches Zentrum Immuntherapie, University Hospital Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Erlangen, Germany.
Deep B-cell and plasma cell depletion is rapidly reshaping the therapeutic landscape. Initially developed for hematologic malignancies, T cell-redirecting therapies (chimeric antigen receptor T cells and T-cell engagers) are now demonstrating profound efficacy in autoimmune diseases. The first successful application of a B-cell maturation antigen-targeting T-cell engager to achieve human leukocyte antigen desensitization in a highly sensitized kidney transplant candidate marks yet another critical milestone: This success signals a "spillover" of deep cell depletion into nonmalignant, nonautoimmune indications and paves the way for novel strategies in transplantation tolerance, severe allergic diseases, and beyond.
Deep B-cell and plasma cell depletion is rapidly reshaping the therapeutic landscape. Initially developed for hematologic malignancies, T cell-redirecting therapies (chimeric antigen receptor T cells and T-cell engagers) are now demonstrating profound efficacy in autoimmune diseases. The first successful application of a B-cell maturation antigen-targeting T-cell engager to achieve human leukocyte antigen desensitization in a highly sensitized kidney transplant candidate marks yet another critical milestone: This success signals a "spillover" of deep cell depletion into nonmalignant, nonautoimmune indications and paves the way for novel strategies in transplantation tolerance, severe allergic diseases, and beyond.
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