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CD70缺乏时的特异性免疫反应和细胞因子产生

Specific Immune Response and Cytokine Production in CD70 Deficiency.

作者信息

Abolhassani Hassan

机构信息

Division of Clinical Immunology, Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, Stockholm, Sweden.

Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Front Pediatr. 2021 Apr 30;9:615724. doi: 10.3389/fped.2021.615724. eCollection 2021.

Abstract

Collective clinical and immunologic findings of defects in the CD27-CD70 axis indicate a primary immunodeficiency associated with terminal B-cell development defect and immune dysregulation leading to autoimmunity, uncontrolled viral infection, and lymphoma. Since the molecular mechanism underlying this entity of primary immunodeficiency has been recently described, more insight regarding the function and profile of immunity is required. Therefore, this study aimed to investigate stimulated antibody production, polyclonal vs. virus-specific T-cell response, and cytokine production of a CD70-deficient patient reported previously with early-onset antibody deficiency suffering from chronic viral infections and B-cell lymphoma. The patient and her family members were subjected to clinical evaluation, immunological assays, and functional analyses. The findings of this study indicate an impaired ability of B cells to produce immunoglobulins, and a poor effector function of T cells was also associated with the severity of clinical phenotype. Reduced proportions of cells expressing the memory marker CD45RO, as well as T-bet and Eomes, were observed in CD70-deficient T cells. The proportion of 2B4 and PD-1 virus-specific CD8 T cells was also reduced in the patient. Although the -mutated individuals presented with early-onset clinical manifestations that were well-controlled by using conventional immunological and anticancer chemotherapies, with better prognosis as compared with CD27-deficient patients, targeted treatment toward specific disturbed immune profile may improve the management and even prevent secondary complications.

摘要

CD27 - CD70轴缺陷的临床和免疫学综合发现表明,这是一种与终末B细胞发育缺陷以及导致自身免疫、病毒感染失控和淋巴瘤的免疫失调相关的原发性免疫缺陷。由于最近已经描述了这种原发性免疫缺陷实体的分子机制,因此需要对免疫功能和特征有更多的了解。因此,本研究旨在调查先前报道的一名CD70缺陷患者的刺激抗体产生、多克隆与病毒特异性T细胞反应以及细胞因子产生情况,该患者患有早发性抗体缺陷、慢性病毒感染和B细胞淋巴瘤。对该患者及其家庭成员进行了临床评估、免疫测定和功能分析。本研究结果表明,B细胞产生免疫球蛋白的能力受损,T细胞的效应功能不佳也与临床表型的严重程度相关。在CD70缺陷的T细胞中,观察到表达记忆标志物CD45RO以及T-bet和Eomes的细胞比例降低。该患者中2B4和PD-1病毒特异性CD8 T细胞的比例也降低。尽管这些突变个体表现出早发性临床表现,通过使用传统免疫疗法和抗癌化疗可以得到很好的控制,与CD27缺陷患者相比预后更好,但针对特定紊乱免疫特征的靶向治疗可能会改善治疗管理,甚至预防继发性并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b15/8120026/ef2dddc4aa76/fped-09-615724-g0001.jpg

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