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. 2020 Feb 18;34(3):363–379. doi: 10.1007/s40259-020-00407-0

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 8 — Evaluation of biosimilarity between HLX02 and the RPs with FcγRIIIa affinity chromatography. a FcγRIIIa affinity chromatographic profiles of the RP batches with high affinity and low affinity. b Comparison of FcγRIIIa binding and ADCC activities for HLX02 and the RPs with low FcγRIIIa affinity or with high FcγRIIIa affinity, respectively. ADCC antibody-dependent cell-mediated cytotoxicity, FcγR Fc gamma receptor, RP reference product