TGN1412 Induces Lymphopenia and Human Cytokine Release in a Humanized Mouse Model

Sabrina Weißmüller, Stefanie Kronhart, Dorothea Kreuz, Barbara Schnierle, Ulrich Kalinke, Jörg Kirberg, Kay-Martin Hanschmann and Zoe Waibler

PLOS ONE, 2016, vol. 11, issue 3, 1-19

Abstract: Therapeutic monoclonal antibodies (mAbs) such as the superagonistic, CD28-specific antibody TGN1412, or OKT3, an anti-CD3 mAb, can cause severe adverse events including cytokine release syndrome. A predictive model for mAb-mediated adverse effects, for which no previous knowledge on severe adverse events to be expected or on molecular mechanisms underlying is prerequisite, is not available yet. We used a humanized mouse model of human peripheral blood mononuclear cell-reconstituted NOD-RAG1-/-Aβ-/-HLADQ(tg+ or tg-)IL-2Rγc-/- mice to evaluate its predictive value for preclinical testing of mAbs. 2–6 hours after TGN1412 treatment, mice showed a loss of human CD45+ cells from the peripheral blood and loss of only human T cells after OKT3 injection, reminiscent of effects observed in mAb-treated humans. Moreover, upon OKT3 injection we detected selective CD3 downmodulation on T cells, a typical effect of OKT3. Importantly, we detected release of human cytokines in humanized mice upon both OKT3 and TGN1412 application. Finally, humanized mice showed severe signs of illness, a rapid drop of body temperature, and succumbed to antibody application 2–6 hours after administration. Hence, the humanized mouse model used here reproduces several effects and adverse events induced in humans upon application of the therapeutic mAbs OKT3 and TGN1412.

Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pone00:0149093

DOI: 10.1371/journal.pone.0149093

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