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. 2020 Jun 26;11:1261. doi: 10.3389/fimmu.2020.01261

Table 2.

Recombinant Immunotoxins that were mutated to decrease immunogenicity.

Drug name Target Toxin description Activity References
IC50 (pM) Relative activity (compared to PE38) (%) Cell type
Moxetumomab CD22 PE38 3.4 100 CA46 (65)
LO10 PE24 with 5 point mutations to reduce B cell binding 0.9 378 (64)
LMB-T18 PE24 with 6 point mutations to reduce T cell binding 2.2 155 (65)
LMB-T19 PE24 with 10 point mutations to reduce B and T cell binding 3.4 100 Unpublished
SS1P Mesothelin PE38 47.5 100 KLM1 (66)
LMB-100/RG7787 Humanized Fab and PE24 with 5 point mutations to reduce B cell binding 9.9 480
LMB-T20 PE24 with 6 point mutations to reduce T cell binding 13.1 363
LMB-T14 PE24 with 10 point mutations to reduce B and T cell binding 27.9 170
LMB-2 CD25 PE38 0.07 100 HUT102 (67)
LMB-2 T20 PE38 with 6 point mutations to reduce T cell binding 0.23 30
LMB-142 PE38 with 9 point mutations to reduce T cell binding 0.69 10
Tac-M18-PE24(T) PE24 with C-C stabilizing linker and 6 point mutations to reduce T cell binding 0.7 10 (68)
LMB-75 BCMA PE24 1.1 100 H929 (69)
PE24 with 4 point mutations to reduce B cell binding 3.1 35 Unpublished
LMB-92
LMB-103 (T20)
PE24 with 6 point mutations to reduce T cell binding 6 18 Unpublished
LMB-273 (T20) PE24 with 5 point mutations to reduce T cell binding (excluding R494A) 1.1 100 Unpublished
HN3-PE38 GPC3 PE38 586.0 100 Hep38B
HN3-mPE24 PE24 with 5 point mutations to reduce B cell binding 592.0 99 (70)
HN3-T20 PE24 with 6 point mutations to reduce T cell binding 766.0 77
HN3-T19 PE24 with 10 point mutations to reduce B and T cell binding 1082.0 54