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A nondepleting anti-CD19 antibody impairs B cell function and inhibits autoimmune diseases
Jeffrey S. Boyles, Dorota Sadowski, Scott Potter, Aleksandra Vukojicic, James Parker, William Y. Chang, Yanfei L. Ma, Mark G. Chambers, James Nelson, Barbra Barmettler, Eric M. Smith, Kara Kersjes, Evan R. Himes, Chaohua Lin, Jonathan Lucchesi, Jaladhi Brahmbhatt, Ramtin Sina, Jennifer A. Martin, Evan Maestri, Christopher M. Wiethoff, Gregory L. Dyas, Matthew D. Linnik, Songqing Na, Derrick R. Witcher, Alison Budelsky, Kira Rubtsova
Jeffrey S. Boyles, Dorota Sadowski, Scott Potter, Aleksandra Vukojicic, James Parker, William Y. Chang, Yanfei L. Ma, Mark G. Chambers, James Nelson, Barbra Barmettler, Eric M. Smith, Kara Kersjes, Evan R. Himes, Chaohua Lin, Jonathan Lucchesi, Jaladhi Brahmbhatt, Ramtin Sina, Jennifer A. Martin, Evan Maestri, Christopher M. Wiethoff, Gregory L. Dyas, Matthew D. Linnik, Songqing Na, Derrick R. Witcher, Alison Budelsky, Kira Rubtsova
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Research Article Immunology

A nondepleting anti-CD19 antibody impairs B cell function and inhibits autoimmune diseases

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Abstract

B cells contribute to multiple aspects of autoimmune disorders, and B cell–targeting therapies, including B cell depletion, have been proven to be efficacious in treatment of multiple autoimmune diseases. However, the development of novel therapies targeting B cells with higher efficacy and a nondepleting mechanism of action is highly desirable. Here we describe a nondepleting, high-affinity anti–human CD19 antibody LY3541860 that exhibits potent B cell inhibitory activities. LY3541860 inhibits B cell activation, proliferation, and differentiation of primary human B cells with high potency. LY3541860 also inhibits human B cell activities in vivo in humanized mice. Similarly, our potent anti-mCD19 antibody also demonstrates improved efficacy over CD20 B cell depletion therapy in multiple B cell–dependent autoimmune disease models. Our data indicate that anti-CD19 antibody is a highly potent B cell inhibitor that may have potential to demonstrate improved efficacy over currently available B cell–targeting therapies in treatment of autoimmune conditions without causing B cell depletion.

Authors

Jeffrey S. Boyles, Dorota Sadowski, Scott Potter, Aleksandra Vukojicic, James Parker, William Y. Chang, Yanfei L. Ma, Mark G. Chambers, James Nelson, Barbra Barmettler, Eric M. Smith, Kara Kersjes, Evan R. Himes, Chaohua Lin, Jonathan Lucchesi, Jaladhi Brahmbhatt, Ramtin Sina, Jennifer A. Martin, Evan Maestri, Christopher M. Wiethoff, Gregory L. Dyas, Matthew D. Linnik, Songqing Na, Derrick R. Witcher, Alison Budelsky, Kira Rubtsova

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Figure 3

LY3541860 inhibits B cell proliferation, activation, and plasmablast differentiation in vitro.

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LY3541860 inhibits B cell proliferation, activation, and plasmablast dif...
(A) Representative data showing a concentration-dependent decrease of B cell proliferation induced by anti-IgM cross-linking in vitro IC50, determined by generating dose-response curves and fitting to a 4 parameter logistic fit of the CCPM values as a function of LY3541860 concentration (mean ± SEM, n = 3). (B) Inhibition of CpG-induced upregulation of CD69 on B cells in human whole blood. Representative data showing a concentration-dependent decrease of percent of CD69+ cells on viable B cells in human whole blood after incubation with CpG for 24 hours. The IC50 was determined by generating dose response curve and fitting to a 4 parameter logistic fit of the percent of CD69+ cells as a function of LY3541860 concentration. Data are shown as mean ± SEM. (C) Inhibition of primary memory B cell differentiation into plasmablasts in the presence of BAFF/IL-21/IL-2/anti-CD40 and different concentrations of either LY3541860 or isotype control as indicated. The graph shows the percent of plasmablasts (identified as CD20lo/CD38hi) in culture. The assay was performed 3 times and data from one representative experiment is shown.

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ISSN 2379-3708

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