Dosing optimization of CCR4 immunotoxin for improved depletion of CCR4+ Treg in nonhuman primates

Recently, we have developed a diphtheria toxin‐based recombinant anti‐human CCR4 immunotoxin for targeting CCR4+ tumors and Tregs. In this study, we further optimized the dosing schedule for improved CCR4+ Treg depletion. We have demonstrated that up to a 90% depletion was achieved and the depletion...

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Veröffentlicht in:Molecular oncology 2018-08, Vol.12 (8), p.1374-1382
Hauptverfasser: Wang, Zhaohui, Louras, Nathan J., Lellouch, Alexandre G., Pratts, Shannon G., Zhang, Huiping, Wang, Haoyu, Huang, Christene A., Cetrulo, Curtis L., Madsen, Joren C., Sachs, David H., Wang, Zhirui
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Sprache:eng
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Zusammenfassung:Recently, we have developed a diphtheria toxin‐based recombinant anti‐human CCR4 immunotoxin for targeting CCR4+ tumors and Tregs. In this study, we further optimized the dosing schedule for improved CCR4+ Treg depletion. We have demonstrated that up to a 90% depletion was achieved and the depletion extended to approximately 2 weeks in the peripheral blood and more than 48 days in the lymph node at 25 μg·kg−1, BID for 8 consecutive days in cynomolgus monkeys. Expansion was observed including monocytes and NK cells. Antibody against the CCR4 immunotoxin was detected after approximately 2 weeks, affecting further depletion efficacy for multiple course treatment. Recently, we have developed a CCR4 immunotoxin capable of depleting human CCR4+ tumors and Tregs. In this study, we further optimized the dosing strategy for improved depletion of CCR4+ Tregs in cynomolgus monkeys. We have extended the depletion to approximately 2 weeks in the peripheral blood and more than 48 days in the lymph node.
ISSN:1574-7891
1878-0261
DOI:10.1002/1878-0261.12331