下一代基于抗体的癌症治疗:抗体-药物偶联物和双特异性抗体在血液系统恶性肿瘤和实体瘤中的应用
Next-generation antibody-based therapeutics in cancer: antibody-drug conjugates bispecific antibodies across hematologic malignancies and solid tumors
肿瘤学的治疗范式正在经历由抗体药物偶联物(ADC)和双特异性抗体(bsAb)驱动的深刻变革。
英文原题:Spatial immune profiling reveals distinct microenvironments in medullary thyroid carcinoma.
这些结果凸显了MTC复杂且具有空间依赖性的免疫景观,提示其对靶向免疫治疗的意义。本研究为MTC的免疫微环境提供了新的见解,并强调需要进一步研究以阐明其对疾病进展和治疗反应的影响。
甲状腺髓样癌(MTC)是一种罕见且侵袭性强的甲状腺癌,预后具有挑战性。虽然免疫微环境在癌症进展中起着至关重要的作用,但与更常见的甲状腺癌相比,其在MTC中的作用仍未被充分探索。
本研究通过系统评估不同组织拓扑结构中免疫细胞浸润和免疫标志物的表达,探讨了MTC的免疫景观。我们采用先进的免疫组织化学技术,分析了24例MTC患者的组织样本,重点关注肿瘤核心、与健康组织的交界处、邻近正常甲状腺组织以及淋巴结转移灶。
我们的研究结果揭示了一种独特的免疫特征,即肿瘤邻近正常组织中CD3+、CD4+、CD8+和CD20+淋巴细胞增多,肿瘤交界处颗粒酶B+细胞显著存在,尤其是在结构性病变患者中。此外,我们在转移组织中观察到肥大细胞的显著富集。
INTRODUCTION: Medullary thyroid carcinoma (MTC) is a rare and aggressive thyroid cancer with a challenging prognosis. While the immune microenvironment plays a crucial role in cancer progression, its role in MTC remains underexplored compared to more common thyroid cancers. METHODS: this study investigates the immune landscape of MTC by systematically evaluating immune cell infiltration and expression of immune markers across various tissue topographies. We utilized advanced immunohistochemical techniques to analyze tissue samples from 24 MTC patients, focusing on the tumor core, interface with healthy tissue, adjacent normal thyroid tissue, and lymph node metastases. RESULTS: our findings reveal a distinct immune profile with increased CD3+, CD4+, CD8+ and CD20+ lymphocytes in normal tissues adjacent to tumors and a notable presence of granzyme B+ cells in the tumor interface, particularly in patients with structural disease. Additionally, we observed a significant enrichment of mast cells in metastatic tissues. DISCUSSION: these results highlight the complex and spatially dependent immune landscape of MTC, suggesting implications for targeted immunotherapy. This study provides novel insights into the immune microenvironment of MTC and emphasizes the need for further research to elucidate its impact on disease progression and therapeutic response.
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