Aim: Obinutuzumab induces NK cell antibody-dependent cell-mediated cytotoxicity.
Objective: Investigate the effects on the human immune system after obinutuzumab monotherapy treatment in patients with chronic lymphocytic leukemia (CLL).
Method: To evaluate these effects, we analyzed the distribution of CD4 and CD8 T cells, B cells and NK cells in the peripheral blood of eight CLL patients who were treated with obinutuzumab in monotherapy. The distribution of peripheral blood lymphocytes was examined prior to each dose of obinutuzumab and 24-72 h after the first 1000 mg complete dose (cycle 1 day 2). We also repeated measurements 3 months after the last obinutuzumab dose. In total we obtained ten samples of each patient. Analyses were performed by flow cytometry with monoclonal antibodies against CD3, CD4, CD8, CD19 and CD56.
Results: After the first 1000 mg obinutuzumab infusion (cycle 1 day 2), CD4 T cells and CD8 T cells were significantly decreased in peripheral blood compared with prior to therapy. This reduction in the CD4 T cells persisted after six cycles of obinutuzumab (1235 cells/μl basal vs 662 cells/μl after six cycles, p ≤ 0.05), but not in CD8 T cells (987 cells/μl basal vs 837 cells/μl after six cycles). Interestingly, we also observed significant differences in the NK cell compartment after the first 1000 mg drug infusion (490 cells/μl basal vs 23 cells/μl postinfusion, p ≤ 0.05), and after cycle 6 (490 cells/μl basal vs 149 cells/μl after six cycles, p ≤ 0.05).
Conclusion: Obinutuzumab induces depletion of NK cells in CLL.
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http://dx.doi.org/10.2217/imt-2017-0147 | DOI Listing |
Zhonghua Xue Ye Xue Za Zhi
November 2024
Peking University People's Hospital & Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing 100044, China.
Front Oncol
December 2024
Department of Hematology, Peking University People's Hospital, National Clinical Research Center for Hematologic Diseases, Peking University Institute of Hematology, Beijing, China.
Background: Obinutuzumab, a humanized type II anti-CD20 monoclonal antibody, is widely used in the treatment of B-cell lymphomas. Thrombocytopenia typically occurs 1 to 2 weeks after administration. In rare cases, obinutuzumab can induce severe acute thrombocytopenia within days of infusion, a condition known as "obinutuzumab-induced acute thrombocytopenia (OIAT).
View Article and Find Full Text PDFAnn Hematol
December 2024
The Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.
The prevalence of anti-CD20 monoclonal antibody (MoAb)-associated delayed-onset neutropenia (DON) varies between 8 and 27%. Despite the wide use of MoAbs as maintenance in follicular lymphoma (FL), data regarding DON occurrence and clinical consequences are limited. This study assessed DON prevalence, severity and risk factors in FL patients during maintenance.
View Article and Find Full Text PDFClin Kidney J
November 2024
Division of Nephrology, Huashan Hospital, Fudan University, Shanghai, China.
Background: Obinutuzumab is a humanized and glycoengineered anti-CD20 monoclonal antibody that has been shown to induce more profound B-cell depletion than rituximab. The effectiveness and safety of obinutuzumab in the treatment of membranous nephropathy remain unclear.
Methods: This was a retrospective study conducted in Huashan Hospital, Fudan University between 1 December 2021 and 30 November 2023.
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