广东韶关地区54 597例女性HPV感染情况及 其基因型分布

目的探讨广东韶关地区女性人乳头瘤病毒(HPV)感染现状及病毒基因型分布情况。方法采用PCR-反向点杂交技术对54 597例女性宫颈脱落细胞标本进行23种HPV基因分型检测。结果 54 597例女性中共检出HPV阳性13 824例,阳性率为25.32%。全部标本中高危型感染占19.91%(10870/54597),主要包含HPV52 (2187/54597)、HPV16 (1852/54597)、HPV58 (1226/54597)、HPV53(801/54597)和HPV68 (729/54597)。低危型感染占5.41%(2954/54597),主要包含HPV43 (896/54597)和HPV81 (833/54597)。感染类型中单一感染占79.22%(8545/10787),二重感染占15.62%(1685/10787),三重及以上感染占5.16%(557/10787)。结论韶关地区女性HPV感染率较高,且以高危型和单一型感染为主。病毒主要基因型为HPV52、HPV16和HPV58。进行HPV基因分型检测对宫颈癌的防治和疫苗研发接种具有重要意义。     

广州市花都区789例人乳头瘤病毒感染状况及其基因型研究

目的 对广州市花都区789例疑似人乳头瘤病毒( HPV)感染的妇女进行调查,研究HPV感染状况和基因亚型分布情况.方法 采用荧光定量聚合酶链式反应(Fluorescence quantitative PCR,FQ-PCR)对789例疑似HPV感染患者的宫颈分泌物进行21种人乳头瘤病毒基因亚型的检测.结果 (1)789例标本中,HPV阳性占48.42％(382/789),共检出10种基因型,其中检出单一低危型(HPV6、11、43和44型)279例,占感染者73.04％;单一高危型( HPV16、18、33、52、53、58)68例,占感染者17.80％;多重感染35例,占感染者9.16％.低危型以HPV6、11为主,高危型以HPV16、18为主.HPV6为主要致病基因型,检出率为34.0％ (P ＜0.01);(2)各年龄段间感染率差异无统计学意义(P＞0.05).结论 花都区HPV感染率较高,且多为单一轻危型感染,以HPV6为主要感染亚型,HPV基因型分布有助于确定宫颈癌发生的高危因素及筛查高危人群,对本地区HPV疫苗开发、应用具有重大意义.     

四川地区宫颈癌HPV59型感染及其E6基因突变

宫颈癌是妇科常见的恶性肿瘤,特定型别的人 乳头瘤病毒(HPV)感染是引发宫颈癌的主要因 素。根据HPV致癌性的不同可分为高危型,低 危型。Munoz N[2]等对来自9个国家的1918例宫 颈癌组织进行各型HPV筛查,最终确认HPV-16、 18、26、31、33、35、39、45、51、52、53、56、58、59、66、 68、73及82型为高危型。李洁等[3]用核酸印迹技 术对1986至1994年间来自我国14个省市自治区 的1008宫颈癌组织进行HPV型别检测,发现 HPV-16、18、31、35、51、58等型的存在,并发现各 地区主要流行型别随地理位置有所差异。     

新疆地区妇女HPV感染的现状与分型

目的对新疆地区妇女HPV基因型的流行和分布进行调查。方法收集新疆医科大学附属肿瘤医院2010年至2017年疑似HPV感染的23 818例门诊女性HPV首次检测结果,检测方法采用人乳头瘤病毒(HPV)分型检测试剂盒(PCR+膜杂交法)。结果新疆地区妇女HPV感染总阳性率为36.17%,HPV单一型感染率为30.29%,HPV多重感染率为5.88%。该地区排名前5位的HPV基因型:HPV6(22.68%)、HPV16(19.95%)、HPV58(3.28%)、HPV52(2.57%)、HPV53(2.46%)。研究还发现汉族妇女HPV感染阳性率为34.63%,其中单一型感染为28.55%,多重感染为6.08%;维吾尔族妇女人群中HPV感染阳性率为40.29%,单一型感染为34.91%,多重感染为5.38%;其他民族中HPV感染阳性率为36.65%,单一型感染为30.96%,多重感染为5.69%。结论新疆地区妇女HPV感染情况日趋严重,迫切需要在该地区开展HPV疫苗接种及筛选工作。     

四川地区宫颈癌HPV59型感染及其E6基因突变

宫颈癌是妇科常见的恶性肿瘤,特定型别的人乳头瘤病毒(HPV)感染是引发宫颈癌的主要因素[1].根据HPV致癌性的不同可分为高危型,低危型.Munoz N[2]等对来自9个国家的1918例宫颈癌组织进行各型HPV筛查,最终确认HPV-16、18、26、31、33、35、39、45、51、52、53、56、58、59、66、68、73及82型为高危型.李洁等[3]用核酸印迹技术对1986至1994年间来自我国14个省市自治区的1008宫颈癌组织进行HPV型别检测,发现HPV-16、18、31、35、51、58等型的存在,并发现各地区主要流行型别随地理位置有所差异.     

13933例妇科门诊患者人乳头瘤病毒感染状况分析

目的探讨河北医科大学第四医院妇科门诊患者人乳头瘤病毒(HPV)感染情况及型别分布情况,为预防HPV感染和宫颈癌防治提供依据。方法采用核酸分子快速导流杂交技术对13 933例妇科门诊患者的宫颈细胞标本进行21种HPV亚型的基因检测,不同年龄组HPV感染率比较采用卡方检验。结果 13933例受检者中,HPV感染5 979例,感染率为42.9%。共计检出21种亚型,9 023例次HPV感染,其中HPV高危型7 823例次占86.7%,感染前三位分别为HPV-16、HPV-52、HPV-58;HPV低危型1 200例次占13.3%,感染前三位分别为HPV-CP8304、HPV-11、HPV-6;17~25岁和≥56岁年龄组HPV感染率相对较高,与其他年龄组比较差异有统计学意义。结论妇科门诊患者HPV感染率较高,且以高危型HPV感染为主,其中最常见的感染亚型是HPV-16、HPV-52、HPV-58。不同年龄组HPV感染率差异有统计学意义,17~25岁和≥56岁年龄组HPV感染率相对较高。     

靖江地区宫颈病变患者高危型人乳头瘤病毒感染及其基因型分析

目的:研究靖江地区各组宫颈病变中高危型人乳头瘤病毒(HPV)感染率及其基因型分布。方法:采用实时荧光PCR检测方法检测334例宫颈脱落细胞标本中高危型HPV及其基因型。结果:高危型HPV在宫颈炎组、湿疣组、低度鳞状上皮细胞内病变(LSIL)组、高度鳞状上皮细胞内病变(HSIL)组中的感染率分别为24.2%、58.2%、49.3%、69.5%;HPV 16、18、33、58型在宫颈病变中是最常见的HPV型别,其中,HPV16型在宫颈炎组、湿疣组、LSIL组、HSIL组中所占比例逐渐增高,分别为17.9%、18.9%、30.8%、41.9%。结论:高危型HPV感染率随着宫颈病变程度的加重而升高,HPV16型是高危型HPV感染中的主要亚型,HPV18、33、52、58也较常见,其余型别很少。     

浙江地区妇女人乳头瘤病毒感染型别及年龄分布现状

目的调查浙江地区妇女人乳头瘤病毒(HPV)的感染现状及型别分布情况,为该地区HPV防治提供流行病学依据。方法采用流式荧光杂交法对浙江地区8 630例妇科门诊妇女的宫颈细胞标本进行27种HPV亚型的基因分型检测,不同年龄组HPV感染率比较采用卡方检验。结果 8 630例受检者中,HPV感染2 125例,感染率为24.62%。27种HPV亚型中,感染率前3位为HPV-52、16、58。54岁和17~24岁年龄组HPV感染率最高,与其他年龄组比较差异有统计学意义。结论不同年龄段HPV感染率差异有统计学意义,54岁和17~24岁年龄组为感染的高危人群;不同年龄段的HPV优势感染型别具有一定的差异性。     

抗女性人群HPV感染和上皮内瘤变的9价HPV疫苗

<正>研究中的抗人乳头状瘤病毒(HPV)的9价病毒样颗粒疫苗包括四价HPV(qHPV)疫苗(6、11、16和18)中HPV型别和5个另外的致癌HPV型别(31、33、45、52、58)。作者对9vHPV疫苗在16至26岁女性人群中的效力和免疫原性研究结果进行了报道。作者进行了由14 215位女性参与的,随机、多国、双盲及2b、|3期的9vHPV疫苗研究。参与者肌     

青海地区46273例女性宫颈HPV检测结果分析

摘要 目的：根据青海地区妇女宫颈人乳头瘤病毒（HPV）检测结果,分析宫颈高危HPV（HR-HPV）感染分布特点,为指导HPV疫苗接种提供理论依据。方法：采用Hybriuax技术检测21种高危型HPV亚型,对2014年1月-2020年2月于我院就诊的46273例女性宫颈人乳头瘤病毒分型检测。结果：46273例妇女中,高危HPV阳性率10.23%,高危HPV阳性率和年龄之间存在线性趋势,随年龄的增大感染比例上升。单一高危亚型HPV感染前三位的HPV亚型为16、58和39,合计占到45.64%。HPV亚型感染以单高危阳性为主,占总HPV阳性数的88.26%,占全部筛查人数的9.03%。HPV16、58、31、68亚型阳性率和年龄段之间存在线性趋势,随年龄的增大感染比例上升。HPV感染亚型检出构成比各年龄段均以HPV16感染排在第一位,排在第二位除61-70岁为双高危外,均为HPV58为主。结论：青海地区女性HPV感染率较高,以单一高危型感染为主,HPV16、58、39、52是主要的感染亚型,所以应针对青海地区HPV感染状况设计具有针对性的预防HPV感染亚型的疫苗。     

Scurvy in capybaras bred in captivity in Argentine

In order to determine if the absence of vitamin C in the diet of capybaras (Hydrochoerus hydrochaeris) causes scurvy, a group of seven young individuals were fed food pellets without ascorbic acid, while another group of eight individuals received the same food with 1 g of ascorbic acid per animal per day. Animals in the first group developed signs of scurvy-like gingivitis, breaking of the incisors and death of one animal. Clinical signs appeared between 25 and 104 days from the beginning of the trial in all individuals. Growth rates of individuals deprived of vitamin C was considerably less than those observed in the control group. Deficiency of ascorbic acid had a severe effect on reproduction of another population of captive capybaras. We found that the decrease in ascorbic acid content in the diet affected pregnancy, especially during the first stages. The results obtained suggest that it is necessary to supply a suitable quantity of vitamin C in the diet of this species in captivity.     

Changes in lactate dehydrogenase activity in chicken tissues in hyperthyreosis in ontogenesis

The lactate dehydrogenase activity in reactions of lactate oxidation and synthesis was studied in subfractions of the chicken brain, heart and liver at the embryonal, early postembryonal and adult stages of development after thyroxine administration. It has been shown that during embryogenesis thyroxine predominantly enhanced the rate of lactate oxidation in the mitochondrial tissues. A marked increase in the lactate synthesis was found in cytoplasm of the adult chicken tissues. Specificity of enzyme activity alterations was detected in the chicken brain during ontogenesis after thyroxine administration.     

Role for dopamine in malonate-induced damage in vivo in striatum and in vitro in mesencephalic cultures

Defects in mitochondrial energy metabolism have been implicated in the pathology of several neurodegenerative disorders. In addition, the reactive metabolites generated from the metabolism and oxidation of the neurotransmitter dopamine (DA) are thought to contribute to the damage to neurons of the basal ganglia. We have previously demonstrated that infusions of the metabolic inhibitor malonate into the striata of mice or rats produce degeneration of DA nerve terminals. In the present studies, we demonstrate that an intrastriatal infusion of malonate induces a substantial increase in DA efflux in awake, behaving mice as measured by in vivo microdialysis. Furthermore, pretreatment of mice with tetrabenazine (TBZ) or the TBZ analogue Ro 4-1284 (Ro-4), compounds that reversibly inhibit the vesicular storage of DA, attenuates the malonate-induced DA efflux as well as the damage to DA nerve terminals. Consistent with these findings, the damage to both DA and GABA neurons in mesencephalic cultures by malonate exposure was attenuated by pretreatment with TBZ or Ro-4. Treatment with these compounds did not affect the formation of free radicals or the inhibition of oxidative phosphorylation resulting from malonate exposure alone. Our data suggest that DA plays an important role in the neurotoxicity produced by malonate. These findings provide direct evidence that inhibition of succinate dehydrogenase causes an increase in extracellular DA levels and indicate that bioenergetic defects may contribute to the pathogenesis of chronic neurodegenerative diseases through a mechanism involving DA.     

SSTR5 ablation in islet results in alterations in glucose homeostasis in mice

Somatostatin (SST) peptide is a potent inhibitor of insulin secretion and its effect is mediated via somatostatin receptor 5 (SSTR5) in the endocrine pancreas. To investigate the consequences of gene ablation of SSTR5 in the mouse pancreas, we have generated a mouse model in which the SSTR5 gene was specifically knocked down in the pancreatic beta cells (betaSSTR5Kd) using the Cre-lox system. Immunohistochemistry analysis showed that SSTR5 gene expression was absent in beta cells at three months of age. At the time of gene ablation, betaSSTR5Kd mice demonstrated glucose intolerance with lack of insulin response and significantly reduced serum insulin levels. Insulin tolerance test demonstrated a significant increase of insulin clearance in vivo at the same age. In vitro studies demonstrated an absence of response to SST-28 stimulation in the betaSSTR5Kd mouse islet, which was associated with a significantly reduced SST expression level in betaSSTR5Kd mice pancreata. In addition, betaSSTR5Kd mice had significantly reduced serum glucose levels and increased serum insulin levels at 12 months of age. Glucose tolerance test at an older age also indicated a persistently higher insulin level in betaSSTR5Kd mice. Further studies of betaSSTR5Kd mice had revealed elevated serum C-peptide levels at both 3 and 12 months of age, suggesting that these mice are capable of producing and releasing insulin to the periphery. These results support the hypothesis that SSTR5 plays a pivotal role in the regulation of insulin secretion in the mouse pancreas.