多发性骨髓瘤
抗体
T细胞受体
免疫学
免疫球蛋白轻链
T细胞
独特型
生物
单克隆抗体
癌症研究
淋巴瘤
免疫球蛋白重链
单克隆
抗原
免疫疗法
B细胞
人类白细胞抗原
医学
过继性细胞移植
分子生物学
白细胞介素21
免疫球蛋白G
移植
化学
受体
骨髓瘤蛋白
人性化鼠标
作者
Karolos Douvlataniotis,Aleksei Titov,Julia Zeun,Merve Bilici,Heyilimu Palashati,Waywen Loh,Even Holth Rustad,Weiwen Yang,Trung T Tran,F. Lund-Johansen,Ravi Chand Bollineni,Jessica D. Kepple,Luis P. Huth,Ludvig A. Munthe,Thorstein Boxaspen,Fredrik Schjesvold,A. Waage,Dimitrios L. Wagner,Katherine R. Bull,Joanna Hester
出处
期刊:Blood
[Elsevier BV]
日期:2026-03-02
被引量:1
标识
DOI:10.1182/blood.2025031897
摘要
T cell-based therapies have shown remarkable efficacy in multiple myeloma (MM), yet the disease remains largely incurable. Here, we investigated the constant domains of the immunoglobulin heavy chain (IgH) as novel targets for therapeutic T cell receptors (TCRs), after confirming high and homogeneous IGH expression in >95% of MM patients. MM cells secrete excessive monoclonal immunoglobulins (M-proteins) that drive complications but are inaccessible to CAR T-cell or antibody targeting. Peptides from IgA and IgG constant regions were eluted from HLA-A*02:01, and reactive TCRs were isolated from healthy donors using allo-HLA-A*02:01 presentation to circumvent self-tolerance. T cells engineered with two TCRs specific for IgA or IgG passed a stringent multi-tier safety screen and selectively eliminated MM cells from 20 HLA-A*02:01+ patients secreting the relevant IgH in vitro. In vivo, IgA-TCR T cells eradicated IgA+HLA-A*02:01+ MM cells in xenograft models and reduced circulating IgA in humanized mice. These findings establish immunoglobulin constant domains as viable TCR targets in MM, potentially making ~40% of patients of European descent eligible for TCR T cell therapy, and extension to additional HLA alleles could further broaden eligibility. The approach may also be applicable to lymphoma and antibody-mediated autoimmune diseases.
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