Development of a deimmunized bispecific immunotoxin dDT2219 against B-cell malignancies

Jorg Uwe Schmohl, Deborah A Todhunter, Elizabeth A Taras, Veronika Bachanova, Daniel A. Vallera

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


Diphtheria toxin (DT) related targeted toxins are effective in cancer treatment, but efficacy diminishes in time because of their immunogenic potential and/or former vaccinations. In order to overcome this limitation for DT2219, a promising bispecific targeted toxin which targets CD19 and CD22, we deimmunized the DT moiety, and thereby developed an exciting improved drug (dDT2219) which still has the potential to sufficiently target B-cell malignancies but also limits clearance because of its reduced immunogenicity. The DT moiety was modified by inducing point mutations in prominent positions on the molecular surface. The new engineered dDT2219 was tested for activity, efficacy, and specificity using functional assays, proliferation assays, and flow cytometry. Furthermore, 12 samples of Chronic Lymphatic Leukemia (CLL) patients were used to assess binding. Immunogenicity was determined using a BALB/c mouse model. dDT2219 was efficient and specific against B-cell malignancies such as Bukitt-Lymphoma cell lines Daudi and Raji. dDT2219 showed specific binding on targets and on CLL samples. Intraperitoneal vaccination of immune competent mice showed that even after multiple administrations with increasing doses, induction of neutralizing antibodies was significantly lower in the dDT2219 treated animal group. The new dDT2219 combines potent anti-tumor cell activity with a reduced immunogenicity. With regard to the frequent development of neutralizing antibodies after multiple administrations with immunotoxins, dDT2219 shows promise to overcome this limitation and thus might maintain effectiveness even after multiple treatment cycles.

Original languageEnglish (US)
Article number32
Issue number1
StatePublished - Jan 6 2018

Bibliographical note

Funding Information:
Acknowledgments: We acknowledge the excellent technical assistance of Andy Sicheneder, and Seunguk Oh. This work was supported in part by the US Public Health Service Grant R01-CA36725 awarded by the NCI and the NIAID, DHHS, the Mayo Partnership Award, the HERA Women’s Cancer Foundation, the Lion Fund, William Lawrence and Blanche Hughes Fund, the Randy Shaver Foundation, the Atwater Cancer Drug Development Award, the Deutsche Krebshilfe (J.U.S.), Germany, and a CETI translational award from the University of Minnesota Masonic Cancer Center.

Publisher Copyright:
© 2018 by the authors. Licensee MDPI, Basel, Switzerland.


  • B-cell malignancies CD19
  • CD22
  • Deimmunized
  • Diphtheria toxin
  • Immunotoxin


Dive into the research topics of 'Development of a deimmunized bispecific immunotoxin dDT2219 against B-cell malignancies'. Together they form a unique fingerprint.

Cite this