A Novel Anti-CD38 Monoclonal Antibody for Treating Immune Thrombocytopenia
- PMID: 38899695
- DOI: 10.1056/NEJMoa2400409
A Novel Anti-CD38 Monoclonal Antibody for Treating Immune Thrombocytopenia
Abstract
Background: Immune thrombocytopenia (ITP) is an autoimmune disease characterized by autoantibody-mediated platelet destruction. Treatment with CM313, a novel anti-CD38 monoclonal antibody, can result in targeted clearance of CD38-positive cells, including plasma cells.
Methods: We conducted a phase 1-2, open-label study to evaluate the safety and efficacy of CM313 in adult patients with ITP. CM313 was administered intravenously at a dose of 16 mg per kilogram of body weight every week for 8 weeks, followed by a 16-week follow-up period. The primary outcomes were adverse events and documentation of two or more consecutive platelet counts of at least 50×109 per liter within 8 weeks after the first dose of CM313. The status of peripheral-blood immune cells in patients and changes in the mononuclear phagocytic system in passive mouse models of ITP receiving anti-CD38 therapy were monitored.
Results: Of the 22 patients included in the study, 21 (95%) had two consecutive platelet counts of at least 50×109 per liter during the treatment period, with a median cumulative response duration of 23 weeks (interquartile range, 17 to 24). The median time to the first platelet count of at least 50×109 per liter was 1 week (range, 1 to 3). The most common adverse events that occurred during the study were infusion-related reaction (in 32% of the patients) and upper respiratory tract infection (in 32%). After CD38-targeted therapy, the percentage of CD56dimCD16+ natural killer cells, the expression of CD32b on monocytes in peripheral blood, and the number of macrophages in the spleen of the passive mouse models of ITP all decreased.
Conclusions: In this study, anti-CD38 targeted therapy rapidly boosted platelet levels by inhibiting antibody-dependent cell-mediated cytotoxicity on platelets, maintained long-term efficacy by clearing plasma cells, and was associated with mainly low-grade toxic effects. (Funded by the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences and others; ClinicalTrials.gov number, NCT05694767).
Copyright © 2024 Massachusetts Medical Society.
Similar articles
-
AMG 531, a thrombopoiesis-stimulating protein, for chronic ITP.N Engl J Med. 2006 Oct 19;355(16):1672-81. doi: 10.1056/NEJMoa054626. N Engl J Med. 2006. PMID: 17050891 Clinical Trial.
-
Tumor Necrosis Factor-α Blockade Corrects Monocyte/Macrophage Imbalance in Primary Immune Thrombocytopenia.Thromb Haemost. 2021 Jun;121(6):767-781. doi: 10.1055/s-0040-1722186. Epub 2021 Jan 14. Thromb Haemost. 2021. PMID: 33469903
-
Rituximab chimeric anti-CD20 monoclonal antibody treatment for adult refractory idiopathic thrombocytopenic purpura.Am J Hematol. 2005 Apr;78(4):275-80. doi: 10.1002/ajh.20276. Am J Hematol. 2005. PMID: 15795920
-
Novel therapies for immune thrombocytopenia.Br J Haematol. 2022 Mar;196(6):1311-1328. doi: 10.1111/bjh.17872. Epub 2021 Oct 5. Br J Haematol. 2022. PMID: 34611885 Review.
-
The pathogenesis of chronic immune thrombocytopenic purpura.Semin Hematol. 2007 Oct;44(4 Suppl 5):S3-S11. doi: 10.1053/j.seminhematol.2007.11.002. Semin Hematol. 2007. PMID: 18096470 Review.
Cited by
-
Mendelian Randomization Analysis Reveals the Causal Relationships Between Autoimmune Diseases and Idiopathic Thrombocytopenic Purpura and the Mediating Role of Immune Cells.Eur J Rheumatol. 2025 Apr 23;12(1):1-7. doi: 10.5152/eurjrheum.2025.24100. Eur J Rheumatol. 2025. PMID: 40377429 Free PMC article.
-
Novel loop structure of human IgG1 Fc fused CD38 targeted bispecific antibodies and their anti-tumor effect in acute myeloid leukemia.J Transl Med. 2025 Jul 28;23(1):849. doi: 10.1186/s12967-025-06827-2. J Transl Med. 2025. PMID: 40721809 Free PMC article.
-
Targeting CD38 in Antibody-Mediated Rejection.Transpl Int. 2025 May 15;38:14343. doi: 10.3389/ti.2025.14343. eCollection 2025. Transpl Int. 2025. PMID: 40444214 Free PMC article. Review.
-
LLT1 overexpression renders allogeneic-NK resistance and facilitates the generation of enhanced universal CAR-T cells.J Exp Clin Cancer Res. 2025 Jan 25;44(1):25. doi: 10.1186/s13046-025-03273-2. J Exp Clin Cancer Res. 2025. PMID: 39856752 Free PMC article.
-
YC-4-3, a Novel Glycogen Synthase Kinase 3β Inhibitor, Alleviates the Endoplasmic Reticulum Stress of Macrophages in Primary Immune Thrombocytopenia.Adv Sci (Weinh). 2025 May;12(17):e2412515. doi: 10.1002/advs.202412515. Epub 2025 Mar 7. Adv Sci (Weinh). 2025. PMID: 40052221 Free PMC article.
References
Publication types
MeSH terms
Substances
Associated data
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials