Efficacy and safety of autologous CD5-KO anti-CD5 CAR-T cells in relapsed/refractory CD5+ hematological malignancies
Chimeric antigen receptor (CAR)-T cell therapy targeting antigens shared with normal T cells requires genetic modifications to prevent fratricide. This phase 1 trial evaluates autologous CD5-targeting CAR-T cells with CD5 gene deletion (CT125A) in seven patients with relapsed/refractory CD5<sup>+</sup> hematologic malignancies. The overall response rate is 85.7%, including four complete responses. All patients experience cytokine release syndrome (six grade 1-2, one grade 3), and two patients develop immune effector cell-associated neurotoxicity syndrome. The most common grade ≥3 adverse events are cytopenia and infection, with unique observations of rash and autoimmune-related events. Post-infusion immunophenotyping shows persistent depletion of CD5<sup>+</sup> T cells and CD19<sup>+</sup> B cells, with reduced CD4/CD8 ratios. The human CD5 knockin murine model reveals skin lesions without significant vital organ involvement. These findings demonstrate CT125A's therapeutic potential in CD5<sup>+</sup> malignancies while highlighting the need for safety optimization. The trial has been registered at ClinicalTrials.gov (NCT04767308).
Authors
- Shengnan Ding
- Xia Mao
- Yuhao Zeng
- Li Zhu
- Jue Wang
- Yi Xiao
- Xiaojian Zhu
- Xiaoxi Zhou
- Jiali Cheng
- Wei Mu
- Jia Wu
Institutions
- University of Pittsburgh Medical Center (US)
- Tongji Hospital (CN)
- First Affiliated Hospital Zhejiang University (CN)
- Huazhong University of Science and Technology (CN)
Publication Details
- Journal
- Cell Reports Medicine
- Published
- 2026-02-01
- DOI
- https://doi.org/10.1016/j.xcrm.2026.102584
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00