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Review

How the discovery of rituximab impacted the treatment of B-cell non-Hodgkin’s lymphomas

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Pages 71-84 | Published online: 27 Feb 2019

Figures & data

Figure 1 Structure of rituximab, a chimeric monoclonal antibody (~30% mouse origin and ~70% human origin).

Notes: The murine variable regions bind specifically to the CD20 antigen on malignant (as well as normal) B cells. The human constant regions allow human effector mechanisms.
Abbreviations: VL, variable domain (light chain); VH, variable domain (heavy chain); CL, constant domain (light chain); CH, constant domain (heavy chain).
Figure 1 Structure of rituximab, a chimeric monoclonal antibody (~30% mouse origin and ~70% human origin).

Figure 2 The various mechanisms of action rituximab uses to kill B cells associated with NHL through binding of the CD20 antigen.

Note: Binding provokes one or more of the following mechanisms: CDC, ADCC, and/or apoptosis.
Abbreviations: NHL, non-Hodgkin’s lymphoma; CDC, complement-dependent cytotoxicity; ADCC, antibody-dependent cellular cytotoxicity.
Figure 2 The various mechanisms of action rituximab uses to kill B cells associated with NHL through binding of the CD20 antigen.

Table 1 Three key clinical trials with rituximab in combination with CHOP for treatment of aggressive B-cell lymphomas