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继发于单纯疱疹病毒脑炎的抗NMDAR和抗GABA_(BR)双阳性自身免疫性脑炎1例报告及文献复习
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作者 赵仲艳 徐志育 +3 位作者 吴婵姬 赵二义 黄丹 黄仕雄 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2024年第1期236-242,共7页
目的:分析1例单纯疱疹病毒性脑炎(HSVE)继发抗N-甲基-D-天冬氨酸受体(NMDAR)和抗γ-氨基丁酸B型受体(GABA_(BR))双阳性自身免疫性脑炎(AE)患者的临床表现及诊疗经过,以提高临床医生对该类病的认识。方法:收集1例HSVE继发抗NMDAR和抗GABA... 目的:分析1例单纯疱疹病毒性脑炎(HSVE)继发抗N-甲基-D-天冬氨酸受体(NMDAR)和抗γ-氨基丁酸B型受体(GABA_(BR))双阳性自身免疫性脑炎(AE)患者的临床表现及诊疗经过,以提高临床医生对该类病的认识。方法:收集1例HSVE继发抗NMDAR和抗GABA_(BR)双阳性AE患者的临床资料,对其诊断和治疗经过进行总结,并结合相关文献进行复习。结果:患者,男性,36岁,以头痛起病,随后出现肢体抽搐,并进展为意识障碍。入院后脑脊液常规生化检测异常,脑脊液单纯疱疹病毒1型(HSV-1) IgG抗体阳性,脑脊液和血清NMDAR抗体检测阳性,头部磁共振成像(MRI)检查提示右侧枕叶白质异常信号,诊断为HSVE继发抗NMDAR脑炎。数月后患者出现精神行为异常、认知障碍和睡眠障碍等症状,血清NMDAR抗体和GABA_(BR)抗体均阳性,诊断为HSVE继发抗NMDAR脑炎和抗GABA_(BR)脑炎。给予激素冲击和静脉注射免疫球蛋白(IVIG)治疗后,患者病情好转出院。随访1年,患者精神症状完全消失,遗留轻度认知功能障碍。结论:HSVE抗病毒治疗有效的恢复期患者临床症状再度恶化时,应高度怀疑继发AE的可能,应尽快完善自身免疫性抗体检测,以期早期诊断,早期治疗,以改善患者预后。 展开更多
关键词 单纯疱疹病毒性脑炎 抗N-甲基-D-门冬氨酸受体抗体 抗γ-氨基丁酸b型受体抗体 自身免疫性脑炎
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Gamma-aminobutyric-acid-B receptor antibodies in limbic encephalitis with small cell lung cancer
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作者 Ke-Qin Liu Sheng-Qiang Yan Min Lou 《Neuroimmunology and Neuroinflammation》 2015年第1期187-189,共3页
Encephalitis associated with antibodies to gamma-aminobutyric-acid B(GABA-B)is a subgroup of autoimmune synaptic encephalitis with typical features of limbic encephalitis and small cell lung cancer(SCLC).We report a c... Encephalitis associated with antibodies to gamma-aminobutyric-acid B(GABA-B)is a subgroup of autoimmune synaptic encephalitis with typical features of limbic encephalitis and small cell lung cancer(SCLC).We report a case of anti-GABA-B receptor encephalitis in a 57-year-old man who presented with seizures,memory loss,and abnormal behavior.He developed partially neurological responses to immunotherapy,but refused comprehensive tumor screening.The symptoms were aggravated again 4 months later.Workup showed antibodies to GABA-B receptors and tumor screening revealed SCLC.It highlights the importance of early screening of underlying tumor and anti-tumor treatment in paraneoplastic cases. 展开更多
关键词 Gamma‑aminobutyric‑acidb receptor antibodies limbic encephalitis small cell lung cancer
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脂多糖对大鼠下丘脑室旁核GABA_BR1阳性神经元的激活作用 被引量:2
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作者 贾宏阁 袁莲芳 赵钢 《第四军医大学学报》 北大核心 2008年第16期1444-1447,共4页
目的:探讨大鼠下丘脑室旁核(PVN)-氨基丁酸B受体亚单位1(GABABR1)阳性神经元对脂多糖(LPS)刺激的反应.方法:将大鼠腹腔注射LPS建立免疫应激模型,对照组注射等量的生理盐水,采用免疫荧光双标记与激光共聚焦显微镜技术,观察大鼠下丘脑室... 目的:探讨大鼠下丘脑室旁核(PVN)-氨基丁酸B受体亚单位1(GABABR1)阳性神经元对脂多糖(LPS)刺激的反应.方法:将大鼠腹腔注射LPS建立免疫应激模型,对照组注射等量的生理盐水,采用免疫荧光双标记与激光共聚焦显微镜技术,观察大鼠下丘脑室旁核内神经元Fos和GABABR1的标记情况以及它们在同一神经元内是否有共标记.结果:腹腔注射LPS可使大鼠PVN内表达Fos神经元数量显著增高,且PVN内部分神经元可同时被Fos和GABABR1双重标记,双重标记的神经元大约占Fos神经元的30%,占GAB-ABR1的24%.结论:下丘脑室旁核部分GABABR1阳性神经元参与了LPS诱导的免疫应激反应,它们可能在下丘脑-垂体-肾上腺轴的调节方面起重要作用. 展开更多
关键词 脂多糖类 基因 Fos γ-氨基丁酸b受体亚单位1(GAbAb R1) 荧光抗体技术 下丘脑室旁核(PVN) 应激
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以癫痫发作起病的抗GABAB受体脑炎六例 被引量:5
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作者 徐秦岚 崔韬 +2 位作者 史伟雄 王群 李志梅 《脑与神经疾病杂志》 2018年第7期405-410,共6页
目的总结抗r氨基丁酸B型(GABAB)受体脑炎的临床特征以利于早期诊断及治疗。方法对6例抗GABAB受体脑炎患者的临床、实验室、脑电图(EEG)及影像学资料进行分析,并对其进行10~19(13.5±3.1)个月的随访。结果该组患者均以癫痫发作起病,... 目的总结抗r氨基丁酸B型(GABAB)受体脑炎的临床特征以利于早期诊断及治疗。方法对6例抗GABAB受体脑炎患者的临床、实验室、脑电图(EEG)及影像学资料进行分析,并对其进行10~19(13.5±3.1)个月的随访。结果该组患者均以癫痫发作起病,表现为部分性发作、全面强直阵挛发作。5例出现认知功能减退,4例出现精神行为异常。发作间期EEG 1例表现为右前中颞区棘慢波,余未见明显异常。头颅MRI示2例颞叶内侧、海马T2/FLAIR高信号,1例海马体积缩小。腰穿检查2例脑脊液(CSF)压力增高,1例白细胞数增多,4例蛋白升高。所有患者血清及CSF GABAB受体抗体阳性,1例患者血清Hu抗体弱阳性。胸CT示2例肺部占位、2例肺叶微结节、1例纵隔稍大淋巴结及肝脏顶部异常强化灶,4例经活检诊断为小细胞肺癌。抗癫痫药物对患者癫痫发作控制不佳,免疫治疗及抗肿瘤治疗有效。结论抗GABAB受体脑炎可以癫痫发作为首发症状,逐渐出现认知障碍和精神症状,需注意对该类患者进行肿瘤筛查及随访,早期免疫治疗及抗肿瘤治疗可以改善患者神经功能预后。 展开更多
关键词 抗r氨基丁酸b型受体抗体 脑炎 认知功能障碍 精神异常 小细胞肺癌
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Limbic Encephalitis Associated with Anti-y-aminobutyric Acid B Receptor Antibodies: A Case Series from China 被引量:40
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作者 Hong-Zhi Guan Hai-Tao Ren +7 位作者 Xun-Zhe Yang Qiang Lu Bin Peng Yi-Cheng Zhu Xiao-Qiu Shao Yong-Qiang Hu Dong Zhou Li-Ying Cui 《Chinese Medical Journal》 SCIE CAS CSCD 2015年第22期3023-3028,共6页
Background: Autoimmune encephalitis associated with antibodies against γ-aminobutyric acid B receptor (GABABR) in patients with limbic encephalitis (LE) was first described in 2010. We present a series of klan C... Background: Autoimmune encephalitis associated with antibodies against γ-aminobutyric acid B receptor (GABABR) in patients with limbic encephalitis (LE) was first described in 2010. We present a series of klan Chinese patients tbr further clinical refinement. Methods: Serum and cerebrospinal fluid (CSF) samples from patients referred to the program of encephalitis and paraneoplastic syndrome of Peking Union Medical College Hospital were tested with indirect immunofluorescence. Clinical information of patients with anti-GABABR antibody positivity was retrospectively reviewed, and descriptive statistical analysis was performed. Results: All eighteen anti-GABABR antibody-positive cases had limbic syndromes, and electroencephalogram (EEG) or neuroimaging evidence fulfilled the diagnostic criteria of LE. Four patients had additional antibodies against Hu in serum and one had anti-N-methyl-d-aspartate receptor antibody in both sera and CSF. Seventeen (17/18) patients presented with new-onset refractory seizure or status epileptics. Twelve (12/18) patients had memory deficits, 11 (11/18) patients had personality change, 7 (7/18) patients had disturbance of consciousness, and 3 (3/18) patients showed cerebellar dysfunction. One patient with LE had progressive motor and sensory polyneuropathy. Lung cancer was detected in 6 (6/18) patients. Ten (10/18) patients showed abnormality in bilateral or unilateral mediotemporal region on magnetic resonance imaging. Ten (10/18) patients had temporal lobe epileptic activity with or without general slowing on EEG. Seventeen patients received immunotherapy and 15 of them showed neurological improvement. Four patients with lung cancer died within 1-12 months due to neoplastic complications. Conclusions: Our study demonstrates that most Han Chinese patients with anti-GABABR antibody-associated LE have prominent refractory epilepsy and show neurological improvement on immunotherapy. Patients with underlying lung tumor have a relatively poor prognosis. Testing for anti-GABABR antibodies is necessary for patients with possible LE or new-onset epilepsy with unknown etiology. 展开更多
关键词 Anti-γ-aminobutyric acid b receptor antibody Autoimmune: Limbic Encephalitis SEIZURE
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抗γ-氨基丁酸B型受体脑炎的临床特征 被引量:1
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作者 卢凯 朱遂强 《临床神经病学杂志》 CAS 2022年第1期40-44,共5页
目的分析抗GABA B型受体(GABA;R)脑炎的临床特征,血清和CSF抗体敏感度、滴度变化以及癫痫的治疗。方法回顾性分析13例抗GABA;R脑炎患者的临床资料。结果本组男性8例(61.5%),女性5例(38.5%);中位年龄52岁(41~61岁)。10例(76.9%)首发症状... 目的分析抗GABA B型受体(GABA;R)脑炎的临床特征,血清和CSF抗体敏感度、滴度变化以及癫痫的治疗。方法回顾性分析13例抗GABA;R脑炎患者的临床资料。结果本组男性8例(61.5%),女性5例(38.5%);中位年龄52岁(41~61岁)。10例(76.9%)首发症状为癫痫。所有患者均出现痫性发作,10例(76.9%)记忆力下降,10例(76.9%)精神行为异常,3例(23.1%)合并肺癌。血清和CSF抗GABA;R抗体敏感度为90.9%。6例患者行免疫治疗后复查抗GABA;R抗体,4例症状好转后抗体滴度明显下降,2例症状加重后抗体滴度升高。经过免疫治疗和抗癫痫药物治疗,6个月后,72.7%的患者癫痫无发作,36.4%的患者需抗癫痫药物治疗;24个月时,100%的患者癫痫无发作,仅10%的患者仍需抗癫痫药物治疗。结论抗GABA;R脑炎多见于中老年男性,常合并肿瘤,主要表现为癫痫发作、记忆力下降、精神行为异常等。为了避免漏诊,建议同时送检血清和CSF检测抗体。大多数抗GABA;R脑炎患者不需要长期使用抗癫痫药物。 展开更多
关键词 癫痫 抗体滴度 自身免疫性脑炎 抗γ-氨基丁酸b受体脑炎
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呈典型双峰脑炎表型的单纯疱疹病毒脑炎继发自身免疫性脑炎 被引量:4
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作者 高煜 王向波 +1 位作者 闫鹤立 马红梅 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2021年第8期449-454,共6页
目的探讨单纯疱疹病毒脑炎(herpes simplex virus encephalitis,HSE)继发自身免疫性脑炎(autoimmune encephalitis,AE)的临床特征。方法收集7例HSE继发AE患者的临床资料,回顾性分析HSE和AE两病程阶段临床表现、脑脊液检查、AE相关抗体... 目的探讨单纯疱疹病毒脑炎(herpes simplex virus encephalitis,HSE)继发自身免疫性脑炎(autoimmune encephalitis,AE)的临床特征。方法收集7例HSE继发AE患者的临床资料,回顾性分析HSE和AE两病程阶段临床表现、脑脊液检查、AE相关抗体检测、影像学表现,治疗及转归。结果7例患者中男5例,女2例,中位发病年龄27(范围16~45)岁。HSE症状首发距AE症状出现的时间间隔为27(范围18~55)d。AE期症状包括精神行为异常5例(5/7),认知功能障碍3例(3/7),癫痫发作3例(3/7),记忆力减退2例(2/7),意识障碍1例(1/7),语言障碍1例(1/7),肢体运动障碍1例(1/7)。AE期7例(7/7)抗N-甲基-D-天冬氨酸受体(N-methyl-D-aspartate receptor,NMDAR)抗体均阳性;1例(1/7)合并抗γ-氨基丁酸B受体(γ-aminobutyric acid-A/B receptor,GABABR)抗体阳性;2例(2/4)合并髓鞘少突胶质细胞糖蛋白(myelin oligodendrocyte glycoprotein,MOG)抗体阳性。AE期3例(3/7)出现新发病灶,4例(4/7)无新发病灶。AE期7例均给予一线免疫治疗,1例加用长程免疫治疗。随访5(范围3~8)个月间,7例均预后良好,2例部分遗留HSE期出现的功能障碍。结论HSE继发AE呈现双相病程。AE期抗体由阴性转为阳性,抗NMDAR抗体最常见,还可见抗GABABR、MOG抗体,头颅MRI可见新发病灶,新病灶的出现可能与MOG抗体介导的免疫损伤有关。继发AE对免疫治疗反应良好,但患者可遗留HSE造成的神经功能损伤。 展开更多
关键词 单纯疱疹病毒脑炎 自身免疫性脑炎 N-甲基-D-天冬氨酸受体抗体 γ-氨基丁酸b型受体抗体 髓鞘少突胶质细胞糖蛋白抗体
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Electroacupuncture-induced activation of GABAergic system alleviates airway inflammation in asthma model by suppressing TLR4/MyD88/NF-κB signaling pathway 被引量:2
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作者 Ruisong Gong Xiaowen Liu Jing Zhao 《Chinese Medical Journal》 SCIE CAS CSCD 2023年第4期451-460,共10页
Background: Electroacupuncture (EA) has been shown to attenuate airway inflammation in asthmatic mice;however, the underlying mechanism is not fully understood. Studies have shown that EA can significantly increase th... Background: Electroacupuncture (EA) has been shown to attenuate airway inflammation in asthmatic mice;however, the underlying mechanism is not fully understood. Studies have shown that EA can significantly increase the inhibitory neurotransmitter γ-aminobutyric acid (GABA) content in mice, and can also increase the expression level of GABA type A receptor (GABAAR). Furthermore, activating GABAAR may relieve inflammation in asthma by suppressing toll-like receptor 4 (TLR4)/myeloid differentiation factor 88 (MyD88)/nuclear factor-kappa B (NF-κB) signaling pathway. Therefore, this study aimed to investigate the role of GABAergic system and TLR4/MyD88/NF-κB signaling pathway in asthmatic mice treated with EA. Methods: A mouse model of asthma was established, and a series of methods including Western blot and histological staining assessment were employed to detect the level of GABA, and expressions of GABAAR and TLR4/MyD88/NF-κB in lung tissue. In addition, GABAAR antagonist was used to further validate the role and mechanism of GABAergic system in mediating the therapeutic effect of EA in asthma. Results: The mouse model of asthma was established successfully, and EA was verified to alleviate airway inflammation in asthmatic mice. The release of GABA and the expression of GABAAR were significantly increased in asthmatic mice treated with EA compared with untreated asthmatic mice ( P < 0.01), and the TLR4/MyD88/NF-κB signaling pathway was down-regulated. Moreover, inhibition of GABAAR attenuated the beneficial effects of EA in asthma, including the regulation of airway resistance and inflammation, as well as the inhibitory effects on TLR4/MyD88/NF-κB signaling pathway. Conclusion: Our findings suggest that GABAergic system may be involved in mediating the therapeutic effect of EA in asthma, possibly by suppressing the TLR4/MyD88/NF-κB signaling pathway. 展开更多
关键词 ELECTROACUPUNCTURE ASTHMA gamma-aminobutyric acid receptors GAbA Toll-like receptor 4 Myeloid differentiation factor 88 NF-kappa b
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抗γ氨基丁酸B受体脑炎研究进展 被引量:3
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作者 吴燕 苏志强 丁婉秋 《中国临床神经科学》 2022年第2期231-235,F0003,共6页
自身免疫性脑炎(AE)是指免疫系统产生针对神经元抗原的自身抗体而引起的一类脑炎,抗γ氨基丁酸B受体(GABABR)脑炎是一种罕见的与抗神经元细胞表面抗体相关的AE。近年有关抗GABABR脑炎国内外研究报道逐渐增多,文中搜集了国内外该类型脑... 自身免疫性脑炎(AE)是指免疫系统产生针对神经元抗原的自身抗体而引起的一类脑炎,抗γ氨基丁酸B受体(GABABR)脑炎是一种罕见的与抗神经元细胞表面抗体相关的AE。近年有关抗GABABR脑炎国内外研究报道逐渐增多,文中搜集了国内外该类型脑炎的研究现状,并对其临床表现、辅助检查、治疗及预后等研究进展进行综述。 展开更多
关键词 抗γ氨基丁酸b受体脑炎 自身免疫性脑炎 抗神经元细胞表面抗体
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三例不同类型的抗神经元表面抗原抗体阳性的边缘性脑炎患者的临床分析及比较 被引量:6
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作者 刘丽萍 周玉颖 +2 位作者 张淼 张惠红 陆达 《中华神经医学杂志》 CAS CSCD 北大核心 2016年第6期633-638,共6页
目的对3例不同类型的抗神经元表面抗原抗体阳性的边缘性脑炎患者的临床特点进行分析及比较。方法回顾性收集自2011年11月至2015年2月在天津市环湖医院神经内科收治的3例不同类型的抗神经元表面抗原抗体阳性的边缘性脑炎患者的临床资料... 目的对3例不同类型的抗神经元表面抗原抗体阳性的边缘性脑炎患者的临床特点进行分析及比较。方法回顾性收集自2011年11月至2015年2月在天津市环湖医院神经内科收治的3例不同类型的抗神经元表面抗原抗体阳性的边缘性脑炎患者的临床资料,分别为抗N-甲基坷.天门冬氨酸(NMDA)受体脑炎(例1)、富亮氨酸胶质瘤失活因子(LGn)抗体阳性的边缘性脑炎(例2)和γ-氨基丁酸B(GABAB)受体抗体阳性的边缘性脑炎(例3),分析并比较其在临床表现、辅助检查、治疗及预后等方面的特点。结果3例边缘性脑炎均有边缘系统受损相关的认知障碍、精神症状、癫痫发作、运动障碍及头MRI的T2WI或FLAIR出现高信号等表现:但由于不同的自身抗体介导,又有各自不同的特点。例1患者为年轻女性,表现出特异的口.面部异常运动、大量唾液分泌及中枢性低通气,予气管切开及机械通气,腹盆部CT提示伴发卵巢畸胎瘤。例2存在类似面.臂肌张力障碍发作的表现。例3在肾透明细胞癌术后发病,以癫痫大发作为主要表现。无论伴发肿瘤与否,3例均对免疫治疗反应较好,但均遗留不同程度的认知损害。结论由不同类型的抗神经元表面抗原抗体介导的边缘性脑炎有各自不同的临床特点,但均对免疫治疗敏感。 展开更多
关键词 边缘性脑炎 抗神经元表面抗原抗体 抗N-甲基-D-天门冬氨酸受体脑炎 富亮氨酸胶质瘤失活因子抗体 γ-氨基丁酸b受体抗体
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