Cytotoxic Potency of CD22‐Ricin A Depends on Intracellular Routing Rather than on the Number of Internalized Molecules

Cytotoxicity of immunotoxins (ITs) varies considerably depending on factors like the capability of the target antigen to internalize IT molecules, intracellular processing and routing of the IT. We studied factors that may influence cytotoxicity of CD22-ricin A IT to several B cell lines. The antigen density varied from 5.9 × 103 to 6.0 × 104 molecules/cell. The ID50, determined by protein synthesis inhibition, varied from 2.1 × 10−12 to 3.8 × 10−1 M IT in absence and from 2.8 × 10−14 M to 5.2 × 10−12 M IT in presence of the cytotoxicity enhancer NH4C1 (6mM). In absence as well as in presence of NH4C1 no correlation could be found between antigen density and ID50. No relation was observed either with the rate of cytotoxicity. Even in cell lines with a low antigen density, such as KM3, protein synthesis was quickly inhibited. In order to investigate whether the cytotoxicity was dependent on the number of internalized molecules the kinetics of internalization and exocytosis of degraded 125I-labelled CD22 molecules were studied. After 24 h the number of internalized CD22 molecules was highest in Ramos (154, 500), followed by Daudi (110, 300) and KM3 (69, 900). However, despite the higher internalization rate of Daudi the rate of cytotoxicity of 10−8 M IT was comparable with KM3. NH4C1 did not influence the number of internalized molecules but postponed degradation of CD22. In conclusion, CD22-ricin A is a very potent and fast acting IT even for elimination of target cells that express low numbers of antigen. These results may have implication for treatment of different B cell malignancies with CD22-ricin A.