不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Detection of Aberrant CD58 Expression in a Wide Spectrum of Lymphoma Subtypes: Implications for Treatment Resistance.
Detection of Aberrant CD58 Expression in a Wide Spectrum of Lymphoma Subtypes: Implications for Treatment Resistance.
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CD58或淋巴细胞功能相关抗原-3,是T细胞和NK细胞上CD2受体的配体,是其激活和靶细胞杀伤所必需的。我们最近显示,与应答者相比,在CAR-T 细胞治疗后进展的弥漫性大B细胞淋巴瘤(DLBCL)患者中,CD58异常频率呈较高趋势。鉴于CD58状态可能是T细胞介导治疗失败的重要衡量指标,我们开发了一种CD58免疫组织化学检测方法,并评估了748例淋巴瘤中的CD58状态。
我们的结果显示,CD58蛋白表达在B细胞、T细胞和NK细胞淋巴瘤所有亚型中的相当一部分中下调。CD58缺失与DLBCL的不良预后指标显著相关,并与间变性大细胞淋巴瘤中的ALK和DUSP22重排相关。
然而,它与任何淋巴瘤亚型的总生存期或无进展生存期均无关。随着CAR-T 细胞治疗的适用资格正在扩展到更广泛的淋巴瘤谱系,耐药机制,如靶点下调和CD58缺失,可能会限制治疗成功。
因此,CD58状态是淋巴瘤患者中的一个重要生物标志物,这些患者可能受益于下一代T细胞介导疗法或其他减轻免疫逃逸的新方法。
CD58 or lymphocyte function-associated antigen-3, is a ligand for CD2 receptors on T and NK cells and is required for their activation and target cell killing.
We recently showed a trend toward higher frequency of CD58 aberrations in patients with diffuse large B-cell lymphoma (DLBCL) who progressed on chimeric antigen receptor-T-cell treatment compared with those who responded. Given that CD58 status may be an important measure of T-cell-mediated therapy failure, we developed a CD58 immunohistochemical assay and evaluated CD58 status in 748 lymphomas.
Our results show that CD58 protein expression is downregulated in a significant proportion of all subtypes of B-, T-, and NK-cell lymphomas. CD58 loss is significantly related to poor prognostic indicators in DLBCL and to ALK and DUSP22 rearrangements in anaplastic large-cell lymphoma.
However, it is not associated with overall or progression-free survival in any of the lymphoma subtypes. As eligibility for chimeric antigen receptor-T-cell therapy is being extended to a broader spectrum of lymphomas, mechanisms of resistance, such as target downregulation and CD58 loss, may limit therapeutic success. CD58 status is therefore an important biomarker in lymphoma patients who may benefit from next-generation T-cell-mediated therapies or other novel approaches that mitigate immune escape.
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