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Commentary on “A Vaccine for Photodynamic Immunogenic Cell Death: Tumor Cell Caged b y Cellular Disulfide–Thiol Exchange for Immunotherapy” 《一种光动力免疫原性细胞死亡疫苗:细胞二硫化物-硫醇交换法免疫治疗肿瘤细胞》评论
Pub Date : 2021-10-10 DOI: 10.33696/immunology.3.109
J. Zang, Haiqing Dong
Tumor immunotherapy, including monoclonal antibody of immune checkpoint blockade, therapeutic antibody, cancer vaccine and cell therapy, etc., is to restart and maintain the tumor immune cycle, restore the normal antitumor immune response of the body, so as to control and eliminate the tumor [1,2]. Among them, tumor vaccine, which can elicit robust immune response and produce sustained immune memory effect, is particularly favored in the treatment and prevention of tumor recurrence [3,4]. Notably, compared with specific antigen vaccine, whole cell vaccine does not need complex antigen screening and purification process, and can provide all antigens of specific tumor, so it has great prospects [5,6]. Nevertheless, the immune effect of whole cell vaccine is not satisfactory because of its low immunogenicity and limitation efficiency of antigen presentation [7,8].
肿瘤免疫疗法,包括免疫检查点阻断单克隆抗体、治疗性抗体、癌症疫苗和细胞治疗等,是为了重启和维持肿瘤免疫循环,恢复机体正常的抗肿瘤免疫反应,从而控制和消除肿瘤[1,2]。其中,肿瘤疫苗能够引发强大的免疫反应并产生持续的免疫记忆效应,在治疗和预防肿瘤复发方面尤其受青睐[3,4]。值得注意的是,与特异性抗原疫苗相比,全细胞疫苗不需要复杂的抗原筛选和纯化过程,可以提供特异性肿瘤的所有抗原,因此具有很大的前景[5,6]。然而,全细胞疫苗的免疫效果并不令人满意,因为其免疫原性低,抗原呈递效率有限[7,8]。
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引用次数: 0
Expression of Pu.1, C/Ebp? and Bach1 Transcription Factors in Immune Cells in Patients with Cancer Pu.1,C/Ebp的表达?癌症患者免疫细胞中Bach1转录因子的表达
Pub Date : 2021-10-10 DOI: 10.33696/immunology.3.106
G. Zakiryanova, E. Kustova, N. Urazalieva, Emile T. Baimukhametov, V. A. Makarov, G. Shurin, Narymzhan N. Nakisbekov, M. Shurin
Gulnur K. Zakiryanova1*, Elena Kustova2, Nataliya T. Urazalieva2, Emile T. Baimukhametov3, Valeriy A. Makarov4, Galina V. Shurin6, Narymzhan N. Nakisbekov5, Michael R. Shurin6* 1Al-Farabi Kazakh National University, Almaty, Kazakhstan 2Laboratory of Immunology, Scientific Center of Pediatric and Children Surgery, Almaty, Kazakhstan 3Kazakh Medical University of Continuing Education, Department of Oncology, Almaty, Kazakhstan 4Almaty Oncology Center, Department of Oncosurgery, Almaty, Kazakhstan 5Joint Use Center, Atchabarov Scientific Research Institute of Fundamental and Applied Medicine, Asfendiyarov Kazakh National Medical University, Almaty, Kazakhstan 6Departments of Pathology and Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA
Gulnur K.Zakiryanova 1*、Elena Kustova2、Nataliya T.Urazalieva2、Emile T.Baimukhametov3、Valery A.Makarov4、Galina V.Shurin6、Narymzhan N.Nakisbekov5、Michael R.Shurin6*1Al Farabi哈萨克国立大学,哈萨克斯坦阿拉木图2免疫学研究所,儿科和儿童外科科学中心,哈萨克斯坦阿拉木图3哈萨克医科大学继续教育,肿瘤科,哈萨克斯坦阿拉木图4肿瘤肿瘤中心,肿瘤外科,哈萨克斯坦阿拉木图5联合使用中心,Atchabarov基础和应用医学科学研究所,Asfendiyarov哈萨克斯坦国立医科大学,哈萨克斯坦阿拉木图6病理学和免疫学系,匹兹堡大学医学中心,美国宾夕法尼亚州匹兹堡
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引用次数: 0
Novel Combination Treatments for AML AML的新型联合治疗
Pub Date : 2021-10-10 DOI: 10.33696/immunology.3.105
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引用次数: 2
Establishment of an Indirect Enzyme-linked Immunosorbent Assay for Detection of the NS4 Protein of Bluetongue Virus 间接酶联免疫吸附法检测蓝舌病毒NS4蛋白的建立
Pub Date : 2021-09-12 DOI: 10.33696/immunology.4.148
Ji Ma, Xianping Ma, Rang Wang, Fang Li, T. Hu, Huashan Yi
for Detection of the NS4
用于检测NS4
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引用次数: 0
Efficacy of Therapeutic Plasma Exchange Alone or in Combination with Ruxolitinib for the Treatment of Penn Class 3 and 4 Cytokine Release Syndrome Complicating COVID-19 治疗性血浆置换或联合鲁索利替尼治疗Penn 3、4类细胞因子释放综合征合并COVID-19的疗效观察
Pub Date : 2021-09-01 DOI: 10.33696/immunology.3.100
W. L. Gluck, Wesley M. Smith, S. P. Callahan, Robert A. Brevetta, A. Stenbit, J. Martin, Anna V. Blenda, S. Arce, W. Edenfield
Observations early in the viral pandemic of 2020 noted the resemblance between severe coronavirus disease 2019 (COVID-19) infection and the hypercytokinemic state of secondary hemophagocytic lymphohistiocytosis (sHLH) [1]. Conti and colleagues [2] have outlined the binding of COVID-19 to the Toll-like receptor with subsequent cytokine driven fever and pneumonitis, while in Kenderian’s [3] murine model of CRS, ruxolitinib abrogated the development of cytokine excess. Cao [4] reported faster clinical recovery with JAK inhibition and Capochiani’s RESPIRE trial reported an 89% overall response rate (ORR) with ruxolitinib therapy [5]. Discordant findings regarding JAK inhibition have been reported on the superiority of baricitinib plus remdesivir over remdesivir alone in shortening recovery times in hospitalized patients [6] while the randomized RUXCOVID trial failed to impact severe complications of the disease by adding ruxolitinib to standard of care [7]. Other groups [8,9] have reported inflammatory cytokine profiles along with evidence that elevated IL-6 and TNFα are strong predictors of disease severity and survival. While cytokine excess could be an epiphenomenal surrogate for another process, therapeutic strategies have evolved around addressing the excessive cytokine levels complicating a significant fraction of COVID-19 patients.
2020年病毒大流行早期的观察发现,2019年严重冠状病毒病(COVID-19)感染与继发性噬血细胞性淋巴组织细胞病(sHLH)[1]的高细胞动力学状态之间存在相似之处。Conti及其同事已经概述了COVID-19与toll样受体的结合,随后导致细胞因子驱动的发烧和肺炎,而在Kenderian的[3]小鼠CRS模型中,ruxolitinib消除了细胞因子过量的发展。Cao[5]报告了JAK抑制后更快的临床恢复,Capochiani的respiratory试验报告了ruxolitinib治疗[5]的总缓解率(ORR)为89%。关于baricitinib + remdesivir在缩短住院患者恢复时间方面优于单独使用remdesivir的JAK抑制研究结果不一致[6],而随机RUXCOVID试验未能通过将ruxolitinib加入标准护理[7]来影响疾病的严重并发症。其他研究小组[8,9]报道了炎症细胞因子谱,并有证据表明,IL-6和TNFα升高是疾病严重程度和生存率的有力预测因子。虽然细胞因子过量可能是另一种过程的副现象性替代品,但治疗策略已经围绕解决使相当一部分COVID-19患者复杂化的细胞因子水平过高而发展。
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引用次数: 3
Body Mass Index and Covi d-19: Likely Causes for Obesity and Undernutrition Correlation with Disease Severity 体重指数和covid -19:肥胖和营养不良与疾病严重程度相关的可能原因
Pub Date : 2021-09-01 DOI: 10.33696/immunology.3.104
Nicolas Vitale
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引用次数: 0
Environmental Enrichment and Its Benefits for Migraine: Dendritic Cell Extracellular Vesicles as an Effective Mimetic 环境富集及其对偏头痛的益处:树突状细胞胞外囊泡是一种有效的模拟物
Pub Date : 2021-07-16 DOI: 10.33696/immunology.3.102
K. Pusic, L. Won, R. P. Kraig, A. Pusic
Environmental enrichment produces beneficial effects in the brain at genetic, molecular, cellular and behavior levels, and has long been studied as a therapeutic intervention for a wide variety of neurological disorders. However, the complexity of applying a robust environmental enrichment paradigm makes clinical use difficult. Accordingly, there has been increased interest in developing environmental enrichment mimetics, also known as enviromimetics. Here we review the benefits of environmental enrichment for migraine treatment, and discuss the potential of using extracellular vesicles derived from interferon gamma-stimulated dendritic cells as an effective mimetic.
环境富集在遗传、分子、细胞和行为水平上对大脑产生有益影响,长期以来一直被研究为多种神经疾病的治疗干预措施。然而,应用强大的环境富集范式的复杂性使临床使用变得困难。因此,人们对开发环境富集模拟物(也称为环境模拟物)越来越感兴趣。在此,我们回顾了环境富集对偏头痛治疗的益处,并讨论了使用干扰素γ刺激的树突状细胞衍生的细胞外小泡作为有效模拟物的潜力。
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引用次数: 1
Increased Binding Affinity of Furin to D614G Mutant S-glycoprotein May Augment Infectivity of the Predominating SARS-CoV-2 Variant Furin与D614G突变S-糖蛋白结合亲和力的增加可能增强主要严重急性呼吸系统综合征冠状病毒2型变异株的感染性
Pub Date : 2021-06-30 DOI: 10.33696/immunology.3.095
Sardar Sindhu, R. Ahmad, F. Al-Mulla
The coronavirus disease (COVID)-19 pandemic has profoundly devastated human health and wellbeing all over the world, along with colossal setback to global economy in terms of soaring new infections, hospitalizations, ICU admissions, work losses, closures of businesses and institutions, bankruptcies, and precautionary measures involving social distancing, hygiene, and travel restrictions across the globe. COVID-19 was declared by the World Health Organization (WHO) as a public health emergency of international concern in January 2020, and then as a pandemic in March 2020. There are over 154.64 million confirmed coronavirus infections and more than 3.23 million deaths reported to the WHO globally until date (as of 11:21 a.m. CEST, 6 May, 2021) [1]. The disease is caused by a zoonotic positive-sense single-stranded ssRNA virus called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is known to have four structural proteins: spike (S), envelope (E), membrane (M), and nucleocapsid (N), with close genetic similarity to bat coronaviruses. The global science initiative source called “Global Initiative on Sharing Avian Influenza Data” (GISAID) has reported seven SARS-CoV-2 clades as G, GH, GR, L, O, S, and V [2].
冠状病毒病(COVID -19)大流行在全球范围内严重破坏了人类的健康和福祉,同时也给全球经济带来了巨大挫折,包括新感染病例激增、住院、重症监护室入院、失业、企业和机构关闭、破产,以及涉及社交距离、卫生和旅行限制的预防措施。2020年1月,世界卫生组织(世卫组织)宣布COVID-19为国际关注的突发公共卫生事件,然后在2020年3月宣布为大流行。截至目前(截至美国东部时间2021年5月6日上午11点21分),全球向世卫组织报告的冠状病毒确诊病例超过1.5464亿例,死亡病例超过323万例。该疾病是由一种人畜共患的正感单链ssRNA病毒引起的,称为严重急性呼吸综合征冠状病毒2 (SARS-CoV-2),已知该病毒具有四种结构蛋白:刺突(S)、包膜(E)、膜(M)和核衣壳(N),与蝙蝠冠状病毒具有密切的遗传相似性。名为“共享禽流感数据全球倡议”(GISAID)的全球科学倡议来源报告了7个SARS-CoV-2分支,分别为G、GH、GR、L、O、S和V[2]。
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引用次数: 1
Duration of SARS-CoV-2 Infectivity 严重急性呼吸系统综合征冠状病毒2型感染的持续时间
Pub Date : 2021-06-30 DOI: 10.33696/immunology.3.093
Seitz Tamara, Kelani Hasan, Wenisch Christoph, Laferl Hermann
The ongoing SARS-CoV-2 pandemic led to a high number of deaths worldwide as well as an overload of healthcare systems and an economic collapse. One of the reasons can be attributed to the lack of knowledge about the duration of infectivity at the beginning of the pandemic, resulting in hospital isolation of patients and absence periods of employees. In particular, the absence of healthcare workers placed an unprecedented strain on healthcare systems. Thereupon, at least one negative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) test from a respiratory specimen was required for ending isolation [1]. However, prolonged SARS-CoV-2 RNA shedding was reported for several weeks following infection [2-9]. The aim of this paper is to discuss the current state of knowledge about duration of SARS-CoV-2 infectivity and necessity of isolation.
正在进行的SARS-CoV-2大流行导致全球大量死亡,以及医疗保健系统超载和经济崩溃。其中一个原因可归因于在大流行开始时对传染性持续时间缺乏了解,导致医院隔离患者和员工缺勤。特别是,卫生保健工作者的缺乏给卫生保健系统带来了前所未有的压力。因此,至少需要进行一次实时逆转录-聚合酶链反应(RT-PCR)阴性的呼吸标本检测才能结束隔离[1]。然而,据报道,在感染后数周内,SARS-CoV-2 RNA持续脱落[2-9]。本文的目的是讨论关于SARS-CoV-2传染性持续时间和隔离必要性的知识现状。
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引用次数: 2
The Variable Immune Response to SARS-CoV-2 Infection and Potential Treatment with Combination IL-15 and IL-21 对严重急性呼吸系统综合征冠状病毒2型感染的可变免疫反应及IL-15和IL-21联合治疗的潜力
Pub Date : 2021-06-30 DOI: 10.33696/immunology.3.097
S. Wilz
SARS-Cov-2 is the virus that causes the disease COVID-19. The disease has led to the worst worldwide health crisis in 100 years. While many patients remain asymptomatic, most patients develop a mild respiratory infection. Symptoms include cough, fever and chills, fatigue and body aches, headache and loss of the sense of taste or smell. However, a proportion of patients develop severe disease. Symptoms of severe disease include higher fever, hypoxia and respiratory distress, leading to hospitalization, and sometimes the need for mechanical ventilation and ultimately death [1].
SARS-Cov-2是导致COVID-19疾病的病毒。这种疾病导致了100年来最严重的全球健康危机。虽然许多患者仍无症状,但大多数患者会出现轻度呼吸道感染。症状包括咳嗽、发烧和发冷、疲劳和身体疼痛、头痛和味觉或嗅觉丧失。然而,一部分患者会发展成严重的疾病。严重疾病的症状包括高烧、缺氧和呼吸窘迫,导致住院,有时需要机械通气,最终死亡。
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引用次数: 1
期刊
Journal of cellular immunology
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