1st |
Murine–human chimeric |
Rituximab |
Immunogenicity occurs due to chimeric nature |
NHL, CLL, RA, GPA, MPA |
2nd |
Humanized |
Ocrelizumab |
Binds an overlapping epitope region as rituximab. Increased binding affinity. Enhanced ADCC and less CDC compared to rituximab [8, 32] |
RRMS and PPMS |
Veltuzumab |
Complementarity-determining regions are similar to rituximab. Greater binding avidity and effect on CDC than rituximab [8] |
Orphan status designation for ITP and pemphigus |
Obinutuzumab |
Binds to an epitope on CD20 that partially overlaps with that of rituximab. Greater ADCC than rituximab. Unlike rituximab, obinutuzumab does not stabilize CD20 in lipid rafts and thus has less CDC. More effective at direct B cell apoptosis [63] |
With chlorambucil for previously untreated CLL |
Fully human |
Ofatumumab |
Binds to an epitope distinct from that recognized by rituximab, ocrelizumab, veltuzumab, and obinutuzumab. Greater CDC and apoptosis than rituximab [17] |
Refractory or conventional therapy-intolerant CLL |