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Multiprong CD38 targeting to enhance anti-PD1 immune checkpoint blockade efficacy. 多管齐下以 CD38 为靶点,提高抗 PD1 免疫检查点阻断疗法的疗效。
IF 7.2 2区 医学 Pub Date : 2024-09-12 DOI: 10.1080/2162402x.2024.2400429
Vishnu Vijay Vijayan,Preethi Gopalakrishnan Nair,Shashi Gujar
CD38, a multifunctional enzyme involved in NAD+ catabolism, is hypothesized to act as a metabolic checkpoint for antitumor CD8 T cells. A recent study discovered that, apart from its direct metabolic mechanisms, CD38-mediated RyR2-AKT-TCF1 signaling regulates responsiveness to anti-PD1 cancer therapy at the molecular level. These findings advocate multiprong CD38 targeting to overcome resistance to immune checkpoint blockade therapy.
CD38 是一种参与 NAD+ 分解代谢的多功能酶,被认为是抗肿瘤 CD8 T 细胞的代谢检查点。最近的一项研究发现,除了直接的代谢机制外,CD38 介导的 RyR2-AKT-TCF1 信号在分子水平上调节抗 PD1 癌症疗法的反应性。这些发现主张多管齐下,以 CD38 为靶点克服免疫检查点阻断疗法的抗药性。
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引用次数: 0
Multiplex spatial analysis reveals increased CD137 expression and m-MDSC neighboring tumor cells in refractory classical Hodgkin Lymphoma 多重空间分析揭示了难治性典型霍奇金淋巴瘤中 CD137 表达的增加和邻近肿瘤细胞的 m-MDSC
IF 7.2 2区 医学 Pub Date : 2024-08-10 DOI: 10.1080/2162402x.2024.2388304
José L. Solórzano, Victoria Menendez Garcia, E. Parra, Luisa Solis, Ruth Salazar, M. García‐Cosío, F. Climent, Sara Fernández, Eva Díaz, A. Francisco-Cruz, Joseph Khoury, Mei Jiang, Auriole Tamegnon, Carlos Montalbán, Ignacio Melero, I. Wistuba, Carlos E. De Andrea, Juan F. García
{"title":"Multiplex spatial analysis reveals increased CD137 expression and m-MDSC neighboring tumor cells in refractory classical Hodgkin Lymphoma","authors":"José L. Solórzano, Victoria Menendez Garcia, E. Parra, Luisa Solis, Ruth Salazar, M. García‐Cosío, F. Climent, Sara Fernández, Eva Díaz, A. Francisco-Cruz, Joseph Khoury, Mei Jiang, Auriole Tamegnon, Carlos Montalbán, Ignacio Melero, I. Wistuba, Carlos E. De Andrea, Juan F. García","doi":"10.1080/2162402x.2024.2388304","DOIUrl":"https://doi.org/10.1080/2162402x.2024.2388304","url":null,"abstract":"","PeriodicalId":19683,"journal":{"name":"Oncoimmunology","volume":"10 1","pages":""},"PeriodicalIF":7.2,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141920746","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transcriptomics-based characterization of the immuno-stromal microenvironment in pediatric low-grade glioma 基于转录组学的小儿低级别胶质瘤免疫间质微环境特征描述
IF 7.2 2区 医学 Pub Date : 2024-08-09 DOI: 10.1080/2162402x.2024.2386789
M. Körner, Michael Spohn, U. Schüller, M. Bockmayr
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引用次数: 0
Interplay between oncolytic measles virus, macrophages and cancer cells induces a proinflammatory tumor microenvironment 溶瘤麻疹病毒、巨噬细胞和癌细胞之间的相互作用诱发了促炎性肿瘤微环境
IF 7.2 2区 医学 Pub Date : 2024-07-10 DOI: 10.1080/2162402x.2024.2377830
Camille Chatelain, Laurine Berland, Marion Grard, Nicolas Jouand, Judith Fresquet, Joëlle Nader, Ugo Hirigoyen, Tacien Petithomme, Chantal Combredet, Elvire Pons-Tostivint, Delphine Fradin, Lucas Treps, Christophe Blanquart, Nicolas Boisgerault, Frédéric Tangy, Jean-François Fonteneau
Attenuated measles virus (MV) exerts its oncolytic activity in malignant pleural mesothelioma (MPM) cells that lack type-I interferon (IFN-I) production or responsiveness. However, other cells in t...
减毒麻疹病毒(MV)可在缺乏Ⅰ型干扰素(IFN-Ⅰ)产生或反应能力的恶性胸膜间皮瘤(MPM)细胞中发挥其溶瘤活性。然而,恶性胸膜间皮瘤细胞中的其他细胞也能产生IFN-I。
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引用次数: 0
Peripheral CX3CR1+ T cells combined with PD-1 blockade therapy potentiates the anti-tumor efficacy for lung cancer 外周 CX3CR1+ T 细胞与 PD-1 阻断疗法相结合可增强肺癌的抗肿瘤疗效
IF 7.2 2区 医学 Pub Date : 2024-05-22 DOI: 10.1080/2162402X.2024.2355684
C. Li, Zhen Zhang, Qianfeng Cai, Qitai Zhao, Han Wu, JunRu Li, Yaqing Liu, Xuan Zhao, Jinyan Liu, Y. Ping, J. Shan, Shengli Yang, Yi Zhang
ABSTRACT Identifying tumor-relevant T cell subsets in the peripheral blood (PB) has become a potential strategy for cancer treatment. However, the subset of PB that could be used to treat cancer remains poorly defined. Here, we found that the CX3CR1+ T cell subset in the blood of patients with lung cancer exhibited effector properties and had a higher TCR matching ratio with tumor-infiltrating lymphocytes (TILs) compared to CX3CR1− T cells, as determined by paired single-cell RNA and TCR sequencing. Meanwhile, the anti-tumor activities, effector cytokine production, and mitochondrial function were enhanced in CX3CR1+ T cells both in vitro and in vivo. However, in the co-culture system of H322 cells with T cells, the percentages of apoptotic cells and Fas were substantially higher in CX3CR1+ T cells than those in CX3CR1− T cells. Fas-mediated apoptosis was rescued by treatment with an anti-PD-1 antibody. Accordingly, the combination of adoptive transfer of CX3CR1+ T cells and anti-PD-1 treatment considerably decreased Fas expression and improved the survival of lung xenograft mice. Moreover, an increased frequency of CX3CR1+ T cells in the PB correlated with a better response and prolonged survival of patients with lung cancer who received anti-PD-1 therapy. These findings indicate the promising potential of adoptive transfer of peripheral CX3CR1+ T cells as an individual cancer immunotherapy.
摘要 鉴别外周血(PB)中与肿瘤相关的 T 细胞亚群已成为一种潜在的癌症治疗策略。然而,可用于治疗癌症的外周血亚群仍然定义不清。在这里,我们发现肺癌患者血液中的 CX3CR1+ T 细胞亚群具有效应特性,与 CX3CR1- T 细胞相比,它们与肿瘤浸润淋巴细胞(TILs)的 TCR 匹配率更高。同时,CX3CR1+ T细胞在体外和体内的抗肿瘤活性、效应细胞因子产生和线粒体功能都得到了增强。然而,在 H322 细胞与 T 细胞的共培养系统中,CX3CR1+ T 细胞的凋亡细胞和 Fas 百分比大大高于 CX3CR1- T 细胞。用抗 PD-1 抗体处理后,Fas 介导的细胞凋亡可被挽救。因此,联合应用 CX3CR1+ T 细胞和抗 PD-1 治疗可显著降低 Fas 表达,提高肺异种移植小鼠的存活率。此外,PB 中 CX3CR1+ T 细胞频率的增加与接受抗 PD-1 治疗的肺癌患者的更好反应和生存期延长相关。这些研究结果表明,外周CX3CR1+ T细胞的采用性转移作为一种个体癌症免疫疗法具有广阔的前景。
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引用次数: 0
Memory-like differentiation enhances NK cell responses against colorectal cancer 记忆样分化可增强 NK 细胞对结直肠癌的反应
IF 7.2 2区 医学 Pub Date : 2024-05-07 DOI: 10.1080/2162402x.2024.2348254
Nancy D. Marin, Michelle Becker-Hapak, Wilbur M. Song, Quazim A. Alayo, Lynne Marsala, Naomi Sonnek, Melissa M. Berrien-Elliott, Mark Foster, Jennifer A. Foltz, Jennifer Tran, Pamela Wong, Celia C. Cubitt, Patrick Pence, Kimberly Hwang, Alice Y. Zhou, Miriam T. Jacobs, Timothy Schappe, David A. Russler-Germain, Ryan C. Fields, Matthew A. Ciorba, Todd A. Fehniger
Metastatic (m) colorectal cancer (CRC) is an incurable disease with a poor prognosis and thus remains an unmet clinical need. Immune checkpoint blockade (ICB)-based immunotherapy is effective for m...
转移性结直肠癌(CRC)是一种无法治愈的疾病,预后较差,因此仍是一项尚未满足的临床需求。以免疫检查点阻断(ICB)为基础的免疫疗法对转移性结直肠癌(CRC)有很好的疗效。
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引用次数: 0
Combination of T cell-redirecting strategies with a bispecific antibody blocking TGF-β and PD-L1 enhances antitumor responses 将 T 细胞定向策略与阻断 TGF-β 和 PD-L1 的双特异性抗体相结合可增强抗肿瘤反应
IF 7.2 2区 医学 Pub Date : 2024-04-13 DOI: 10.1080/2162402x.2024.2338558
Antonio Tapia-Galisteo, Iñigo Sánchez-Rodríguez, Javier Narbona, Patricia Iglesias-Hernández, Saray Aragón-García, Anaïs Jiménez-Reinoso, Marta Compte, Shaukat Khan, Takeshi Tsuda, Patrick Chames, Javier Lacadena, Luis Álvarez-Vallina, Laura Sanz
T cell-based immunotherapies for solid tumors have not achieved the clinical success observed in hematological malignancies, partially due to the immunosuppressive effect promoted by the tumor micr...
以T细胞为基础的实体瘤免疫疗法并没有取得血液恶性肿瘤的临床成功,部分原因是肿瘤微粒所产生的免疫抑制效应。
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引用次数: 0
Redoxhigh phenotype mediated by KEAP1/STK11/SMARCA4/NRF2 mutations diminishes tissue-resident memory CD8+ T cells and attenuates the efficacy of immunotherapy in lung adenocarcinoma KEAP1/STK11/SMARCA4/NRF2突变介导的高氧化还原表型会减少组织驻留的记忆CD8+T细胞,并削弱肺腺癌免疫疗法的疗效
IF 7.2 2区 医学 Pub Date : 2024-04-09 DOI: 10.1080/2162402x.2024.2340154
Xue-Wu Wei, Chang Lu, Yi-Chen Zhang, Xue Fan, Chong-Rui Xu, Zhi-Hong Chen, Fen Wang, Xiao-Rong Yang, Jia-Yi Deng, Ming-Yi Yang, Qing Gou, Shi-Qi Mei, Wei-Chi Luo, Ri-Wei Zhong, Wen-Zhao Zhong, Jin-Ji Yang, Xu-Chao Zhang, Hai-Yan Tu, Yi-Long Wu, Qing Zhou
Metabolism reprogramming within the tumor microenvironment (TME) can have a profound impact on immune cells. Identifying the association between metabolic phenotypes and immune cells in lung adenoc...
肿瘤微环境(TME)中的代谢重编程会对免疫细胞产生深远影响。确定肺腺癌细胞代谢表型与免疫细胞之间的关联,是研究肺腺癌细胞代谢表型的关键。
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引用次数: 0
PD-L1+ macrophages suppress T cell-mediated anticancer immunity PD-L1+ 巨噬细胞抑制 T 细胞介导的抗癌免疫力
IF 7.2 2区 医学 Pub Date : 2024-04-04 DOI: 10.1080/2162402x.2024.2338951
Peng Liu, Liwei Zhao, Guido Kroemer, Oliver Kepp
Recently, we showed that an autologous DC-based vaccine induces an increase in immunosuppressive PD-L1+ tumor-associated macrophages (TAM) both in the tumor and the tumor draining lymph nodes, ther...
最近,我们研究发现,基于自体DC的疫苗可诱导肿瘤和肿瘤引流淋巴结中免疫抑制性PD-L1+肿瘤相关巨噬细胞(TAM)的增加,进而诱导免疫抑制性PD-L1+肿瘤相关巨噬细胞的增加。
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引用次数: 0
CCR2 and CCR5 co-inhibition modulates immunosuppressive myeloid milieu in glioma and synergizes with anti-PD-1 therapy CCR2和CCR5联合抑制可调节胶质瘤的免疫抑制性髓系环境,并与抗PD-1疗法协同增效
IF 7.2 2区 医学 Pub Date : 2024-04-04 DOI: 10.1080/2162402x.2024.2338965
Ayush Pant, Brandon Hwa-Lin Bergsneider, Siddhartha Srivastava, Timothy Kim, Aanchal Jain, Sadhana Bom, Pavan Shah, Nivedha Kannapadi, Kisha Patel, John Choi, Kwang Bog Cho, Rohit Verma, Caren Yu-Ju Wu, Henry Brem, Betty Tyler, Drew M. Pardoll, Christina Jackson, Michael Lim
Immunotherapy has revolutionized the treatment of cancers. Reinvigorating lymphocytes with checkpoint blockade has become a cornerstone of immunotherapy for multiple tumor types, but the treatment ...
免疫疗法为癌症治疗带来了革命性的变化。通过检查点阻断重振淋巴细胞已成为多种肿瘤类型免疫疗法的基石,但治疗...
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引用次数: 0
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Oncoimmunology
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