期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
IRE1α调节miRNA34a在高糖诱导的心肌细胞肥大中的作用
1
作者 刘静 李晓莉 +4 位作者 陈蕊蕊 魏婷 艾永飞 李炜 刘慧 《心脏杂志》 CAS 2019年第4期373-378,共6页
目的研究肌醇需求因子(inositol-requiringenzyme,IRE)1α在高糖诱导的心肌细胞肥大中的作用及与miRNA34a的关系。方法分离培养心肌细胞并分为对照组,高糖组,对照+过表达IRE1α组,高糖+过表达IRE1α组。利用IRE1α的腺病毒干预细胞,观... 目的研究肌醇需求因子(inositol-requiringenzyme,IRE)1α在高糖诱导的心肌细胞肥大中的作用及与miRNA34a的关系。方法分离培养心肌细胞并分为对照组,高糖组,对照+过表达IRE1α组,高糖+过表达IRE1α组。利用IRE1α的腺病毒干预细胞,观察高糖条件下其对心肌细胞活力、肥大及心钠肽(ANP)表达的影响。Westernblot检测ANP和IRE1α的表达,qRT-PCR检测ANP、IRE1α和miRNA34a表达,免疫荧光染色检测细胞纯度及横截面积。结果与对照组比较,随着葡萄糖浓度上升,细胞活力持续下降(P<0.05),心肌细胞肥大标志ANP表达增加(P<0.05),IRE1α基因及蛋白表达降低(P<0.05),且于葡萄糖浓度达到30mmol/L最低。与对照组比较,高糖能够降低细胞活力,刺激心肌细胞上调ANP表达(P<0.05),刺激心肌细胞横截面积增大(P<0.05);而过表达IRE1α基因能显著上调心肌细胞的活力水平,降低ANP蛋白及基因的表达,抑制高糖培养下心肌细胞的肥大(P<0.05)。qRT-PCR结果显示,随着血糖浓度上升,miRNA34a表达明显升高,且当过表达IRE1α后,miRNA34a表达明显降低。结论过表达IRE1α基因可有效抑制高糖诱导的心肌细胞肥大,其机制可能与下调miRNA34a表达有关。 展开更多
关键词 内质网应激 IRE1α miRNA34a 心肌细胞肥大 高糖
原文传递
Neutralizing antibody durability and SARS-CoV-2 infection in older adults six months after XBB-containing vaccine booster
2
作者 rui-rui chen Guo-Ping Cao +15 位作者 Xue-Dong Song Mei Lu Ming-Ming Wang Xue-Jun Wang Meng-Fei Wang Shuang-Qing Wang Sheng Wan Guo-Jian Yang Lei Lv Yi-Ming Ma Yi-Man cheng Meng Kong Xue-Juan He Hai-Yan Yang Bing-Dong Zhan Mai-Juan Ma 《Signal Transduction and Targeted Therapy》 2025年第11期6153-6165,共13页
The persistence of XBB-containing vaccine-induced immunity against evolving SARS-CoV-2 variants remains uncertain,particularly in older adults,who are at increased risk of severe outcomes and may experience more rapid... The persistence of XBB-containing vaccine-induced immunity against evolving SARS-CoV-2 variants remains uncertain,particularly in older adults,who are at increased risk of severe outcomes and may experience more rapid immune decline.We previously reported neutralizing antibody(nAb)responses 21 days after a single booster dose of trivalent XBB.1.5(Tri-XBB.1.5),bivalent Omicron XBB(Bi-Omi-XBB),or tetravalent XBB.1(Tetra-XBB.1)vaccines in a cohort of 90 older adults aged>65 years.In this six-month longitudinal follow-up analysis of the same cohort,we assessed nAb durability and SARS-CoV-2 infections to extend our earlier findings.Six months post-vaccination,the nAb titers decreased over time,with 2.5-4.6-fold reductions in the geometric mean titer against the variants KP.3.1.1 and XEC;however,the nAb titer remained detectable in most participants.The Tri-XBB.1.5 vaccine exhibited marginally better antibody persistence than the Bi-Omi-XBB and Tetra-XBB.1 vaccines did,suggesting potential formulation-dependent differences in long-term immunogenicity.Twenty-seven participants experienced SARS-CoV-2 infection,including 11(12.2%)confirmed by rapid antigen testing and 16(17.8%)classified as probably based on serological evidence,with relatively frequent infections in bivalent and tetravalent recipients.Lower nAb titers on day 21 were linked to early infections,whereas late infections reflected antibody waning.Infections transiently increased nAb levels,but the elevated titers were not sustained.These findings highlight the importance of updating booster formulations and improving vaccine designs to address emerging immune-evasive variants. 展开更多
关键词 omicron xbb bi omi xbb older adults SARS CoV neutralizing antibody immunity INFECTION XBB containing vaccine booster DURABILITY
暂未订购
Neutralizing antibody responses to three XBB protein vaccines in older adults
3
作者 Guo-Jian Yang Mei Lu +8 位作者 rui-rui chen Shuang-Qing Wang Sheng Wan Xue-Dong Song Guo-Ping Cao Lei Lv Xue-Juan He Bing-Dong Zhan Mai-Juan Ma 《Signal Transduction and Targeted Therapy》 2025年第3期1541-1551,共11页
The ongoing COVID-19 pandemic has underscored the importance of strong immune defenses against emerging SARS-CoV-2 variants.While COVID-19 vaccines containing XBB subvariants have proven effective in neutralizing new ... The ongoing COVID-19 pandemic has underscored the importance of strong immune defenses against emerging SARS-CoV-2 variants.While COVID-19 vaccines containing XBB subvariants have proven effective in neutralizing new SARS-CoV-2 variants,a gap remains in knowledge regarding neutralizing antibody responses in older adults aged>65 years against these newly emerged variants.This study was therefore undertaken to investigate and compare neutralizing antibody responses to three XBB-containing protein-based vaccines(trivalent XBB.1.5 vaccine,bivalent Omicron XBB vaccine,and tetravalent XBB.1 vaccine)head-to-head in 90 individuals aged>65 years.The results showed that all three XBB-containing vaccines substantially enhanced the neutralizing antibody response,with 100%of vaccinees having detectable antibody titers against ancestral D614G and variants BA.5,XBB.1.5,JN.1,KP.2,and KP.3 after booster immunization.Subsequent analysis indicated that the trivalent XBB.1.5 and tetravalent XBB.1 vaccines elicited higher levels of neutralizing antibodies compared to the bivalent Omicron XBB vaccine.The KP.2 and KP.3 variants displayed antibody resistance comparable to the JN.1 variant.Older adults produce similar neutralizing antibody responses to the vaccines regardless of their underlying medical conditions.These findings indicate that booster vaccination with XBB-containing vaccines can effectively elicit strong neutralizing responses against a number of SARS-CoV-2 variants in older adults over 65 years,which will help guide vaccine strategies in this elderly population. 展开更多
关键词 strong immune defenses neutralizing antibody responses immune defense xbb subvariants xbb protein vaccines older adults COVID emerging SARS CoV variants
暂未订购
上一页 1 下一页 到第
使用帮助 返回顶部