Journal of Virus Eradication最新文献

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Genetic characterization on the nucleoprotein and fusion gene of wild-type measles virus circulating in Shanghai, 2001–2022 2001-2022年上海市流行麻疹野生型病毒核蛋白及融合基因的遗传特征
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2025-03-01 DOI: 10.1016/j.jve.2025.100589
Yunyi Li , Xiaoxian Cui , Ai Lin , Wei Tang , Yuying Yang , Wanju Zhang , Jiayu Hu , Zhi Li , Yanqiu Zhou
{"title":"Genetic characterization on the nucleoprotein and fusion gene of wild-type measles virus circulating in Shanghai, 2001–2022","authors":"Yunyi Li ,&nbsp;Xiaoxian Cui ,&nbsp;Ai Lin ,&nbsp;Wei Tang ,&nbsp;Yuying Yang ,&nbsp;Wanju Zhang ,&nbsp;Jiayu Hu ,&nbsp;Zhi Li ,&nbsp;Yanqiu Zhou","doi":"10.1016/j.jve.2025.100589","DOIUrl":"10.1016/j.jve.2025.100589","url":null,"abstract":"<div><div>Measles is an acute and highly contagious viral disease that poses significant public health challenges globally. Since 2001, continuous virologic surveillance has been conducted in Shanghai, enabling a comprehensive analysis of the evolution of the nucleoprotein (N gene) and fusion gene (F gene) of the measles virus (MeV) over a 21-year period. Between 2001 and 2022, there were a total of 1405 MeV strains isolated by the Shanghai Center for Disease Control and prevention (SCDC), including 6 strains of genotype D8, 8 strains of genotype B3, 12 strains of genotype H1b, and the remaining strains of genotype H1a. Reverse transcription polymerase chain reaction (RT-PCR) was used to amplify the 3′ end of the N gene (450 nt) and the complete sequence of the F gene (1622 nt) from the viral isolates. Sequencing of the RT-PCR products was followed by nucleotide and amino acid phylogenetic analyses. The substitution rates were for the F and N genes in Shanghai were determined to be 0.89 × 10<sup>−3</sup> and 2.20 × 10<sup>−3</sup> substitutions site<sup>/</sup>year, respectively.</div><div>Globally, the nucleotide and amino acid similarities of the N gene among 13,498 MeV isolates ranged from 89.1 %–100.0 % and 90.2 %–100.0 %, respectively. Notably, the F gene exhibited 16 high-amino-acid-mutation sites, most of which differed among H1a MeV strains compared t<u>o</u> the Shanghai-191 vaccine strain. The deletion of the glycosylation site at aa 9–11(NVS) was primarily observed in H1a and H1b of MeV strains. However, critical functional sites in the F gene remained conserved.</div><div>In conclusion, the previously predominant indigenous H1a wild-type measles virus (MeV) has not been detected for over two years, with only imported MeV genotypes currently being identified. It is crucial to strengthen the surveillance of MeV genotypes to facilitate the timely identification and containment of imported measles cases, thereby preventing potential outbreaks.</div></div>","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"11 1","pages":"Article 100589"},"PeriodicalIF":3.5,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143580425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Human CD123+AXL+ dendritic cells express Siglec1 that captures and transmits HIV-1 particles to the T cells 人类CD123+AXL+树突状细胞表达Siglec1,捕获并将HIV-1颗粒传递给T细胞
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2025-02-20 DOI: 10.1016/j.jve.2025.100587
Haisheng Yu , Yinghui Cao , Liang Cheng , Guangming Li , Liguo Zhang , Lishan Su
{"title":"Human CD123+AXL+ dendritic cells express Siglec1 that captures and transmits HIV-1 particles to the T cells","authors":"Haisheng Yu ,&nbsp;Yinghui Cao ,&nbsp;Liang Cheng ,&nbsp;Guangming Li ,&nbsp;Liguo Zhang ,&nbsp;Lishan Su","doi":"10.1016/j.jve.2025.100587","DOIUrl":"10.1016/j.jve.2025.100587","url":null,"abstract":"<div><div>Human dendritic cells (DCs) are classified into three subsets based on their ontogeny, transcriptomes, and functions. During primary human immunodeficiency virus (HIV) infection, DCs in the peripheral tissues capture the HIV-1 particles, migrate to the lymph nodes, transfer the particles to CD4<sup>+</sup> T cells, and initiate infection. However, the identity of the DC subset involved is yet elusive. Hitherto, a novel subset (AXL<sup>+</sup>DCs) has been identified in human blood, which is transcriptomically and functionally distinct from three known subsets. Compared to these, resting AXL<sup>+</sup>DCs express Siglec1 (CD169), capture HIV-1 particles in a CD169-dependent manner, and mediate transinfection. These results suggested that AXL<sup>+</sup> DCs may facilitate HIV-1 transmission and the spread of very early-stage HIV infection in patients. Therapeutic strategies that target AXL<sup>+</sup>DCs or CD169 interaction with HIV-1 may provide pre-exposure protection during the initial stages of HIV-1 infection.</div></div>","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"11 2","pages":"Article 100587"},"PeriodicalIF":3.5,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143679113","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessment of the general population knowledge about the emergence of Nipah virus outbreak in Bangladesh: A nationwide cross-sectional study 对孟加拉国出现尼帕病毒暴发的一般人群知识的评估:一项全国性横断面研究
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2025-01-31 DOI: 10.1016/j.jve.2025.100585
Mobin Ibne Mokbul , Shuvajit Saha , Samiha Nahar Tuli , Fatema Binte Nur , A.M. Khairul Islam , Tariful Islam , Shirsho Shreyan , Alok Bijoy Bhadra , Golam Dastageer Prince , Irfath Sharmin Eva , Mustari Nailah Tabassum , Ferdous Wahid , Md Irfan Bin Kayes , Nazim Hassan Ziad , Mohammad Delwer Hossain Hawlader
{"title":"Assessment of the general population knowledge about the emergence of Nipah virus outbreak in Bangladesh: A nationwide cross-sectional study","authors":"Mobin Ibne Mokbul ,&nbsp;Shuvajit Saha ,&nbsp;Samiha Nahar Tuli ,&nbsp;Fatema Binte Nur ,&nbsp;A.M. Khairul Islam ,&nbsp;Tariful Islam ,&nbsp;Shirsho Shreyan ,&nbsp;Alok Bijoy Bhadra ,&nbsp;Golam Dastageer Prince ,&nbsp;Irfath Sharmin Eva ,&nbsp;Mustari Nailah Tabassum ,&nbsp;Ferdous Wahid ,&nbsp;Md Irfan Bin Kayes ,&nbsp;Nazim Hassan Ziad ,&nbsp;Mohammad Delwer Hossain Hawlader","doi":"10.1016/j.jve.2025.100585","DOIUrl":"10.1016/j.jve.2025.100585","url":null,"abstract":"<div><div>The emergence of the Nipah virus (NiV) poses a significant global health threat, particularly in South-East Asian countries. This cross-sectional nationwide study is a pioneer in assessing knowledge levels of NiV outbreak among the general population in Bangladesh. It was conducted among the general population of Bangladesh from 15th January to 10th February 2024. A conveniently selected sample of individuals participated in the assessment of their knowledge about NiV. A semi-structured questionnaire was used as the data collection tool. After data curation, a total of 2121 responses that met the inclusion criteria were retained for analysis. Among 2121 participants, 69.38 % were aware of NiV. Overall, 62 % demonstrated good knowledge of the virus. The main sources of information were social media (29.9 %), television (25.41 %), educational institutions (18.95 %), newspapers (13.65 %), friends (6.39 %), and workplaces (5.91 %). Multivariate logistic regression analysis showed that participants aged 31–40 years had lower odds of poor knowledge (OR = 0.57, 95 % CI: 0.39–0.82, p &lt; 0.01) compared to those aged 21–30. Females had higher odds of poor knowledge (OR = 1.38, 95 % CI: 1.05–1.81, p = 0.02) than males. Lower education levels were associated with higher odds of poor knowledge. Moreover, non-healthcare workers also had higher odds of poor knowledge compared to healthcare workers. There were regional differences, with varying odds in Rangpur (OR = 0.43, 95 % CI: 0.26–0.70, p &lt; 0.01), Khulna (OR = 1.70, 95 % CI: 1.10–2.61, p = 0.01), and Mymensingh (OR = 2.77, 95 % CI: 1.70–4.53, p &lt; 0.01) compared to Dhaka. The current study underscores the importance of evidence-based educational strategies, and may guide government and policymakers to design future targeted interventions to enhance public health literacy and mitigate the spread of NiV in Bangladesh as well as in its neighbouring countries.</div></div>","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"11 1","pages":"Article 100585"},"PeriodicalIF":3.5,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143146405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of a novel bivalent vaccine candidate against hepatitis A virus and rotavirus using reverse vaccinology and immunoinformatics 利用反向疫苗学和免疫信息学开发一种新的抗甲型肝炎病毒和轮状病毒二价候选疫苗
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2025-01-23 DOI: 10.1016/j.jve.2024.100578
Hassan Yarmohammadi , Abbas Akhavan Sepahi , Mojtaba Hamidi-fard , Mohammadreza Aghasadeghi , Golnaz Bahramali
{"title":"Development of a novel bivalent vaccine candidate against hepatitis A virus and rotavirus using reverse vaccinology and immunoinformatics","authors":"Hassan Yarmohammadi ,&nbsp;Abbas Akhavan Sepahi ,&nbsp;Mojtaba Hamidi-fard ,&nbsp;Mohammadreza Aghasadeghi ,&nbsp;Golnaz Bahramali","doi":"10.1016/j.jve.2024.100578","DOIUrl":"10.1016/j.jve.2024.100578","url":null,"abstract":"<div><div>The hepatitis A virus (HAV) and rotavirus are mainly transmitted through fecal-oral and person-to-person contact, and cause severe gastrointestinal complications and liver disease. This work used reverse vaccinology and immunoinformatic methods to create a novel bivalent vaccine against rotavirus and HAV. The amino acid sequences of HAV-rotavirus proteins (VP1 and VP8∗) were retrieved from the GenBank database. Various computational approaches were employed to predict highly conserved regions and the most immunogenic B-cell and T-cell epitopes of VP8 and VP1 of rotavirus and HAV proteins in both humans and BALB/c. Moreover, the predicted fusion protein was analyzed regarding primary and secondary structures and homology validation. In this study, we used two highly conserved peptide sequences of VP8 and VP1 of rotavirus and HAV that induce T and B cell immunogenicity. According to T-cell epitope prediction, this area comprises 2713 antigenic peptides for HLA class II and 30 HLA class I antigenic peptides, both of which are virtually entirely conserved in the Iranian population. In this study, validation as well as analysis of the secondary and three-dimensional structure of the VP8∗-rotavirus + AAY + HAV-VP1 fusion protein, with the aim of designing a multi-epitope vaccine with different receptors. TLR 3, 4 high immunogenic binding ability with immunological properties and interaction between multi-epitope target and TLR were predicted, and it is expected that the target fusion protein has stable antigenic potency and compatible half-life. The above is suggested as a universal vaccination program.</div></div>","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"11 1","pages":"Article 100578"},"PeriodicalIF":3.5,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143420940","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
3.5 – 00053 Monovalent SMAC mimetics enhance proliferation of HIV-specific CD8 T cells 3.5 - 00053 单价 SMAC 拟态物质能增强艾滋病毒特异性 CD8 T 细胞的增殖能力
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2024-12-01 DOI: 10.1016/j.jve.2024.100410
K. Tanaka, Y. Kim, H. King, M. Roche, S.R. Lewin
{"title":"3.5 – 00053 Monovalent SMAC mimetics enhance proliferation of HIV-specific CD8 T cells","authors":"K. Tanaka,&nbsp;Y. Kim,&nbsp;H. King,&nbsp;M. Roche,&nbsp;S.R. Lewin","doi":"10.1016/j.jve.2024.100410","DOIUrl":"10.1016/j.jve.2024.100410","url":null,"abstract":"","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"10 ","pages":"Page 11"},"PeriodicalIF":3.5,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143181916","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
7.5 – 00009 Postmortem analyses of the central nervous system in individuals with HIV demonstrate that infection of microglia contributes to inflammatory pathways despite viral suppression 7.5 - 00009对艾滋病毒感染者中枢神经系统的死后分析表明,尽管病毒受到抑制,但小胶质细胞的感染有助于炎症途径
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2024-12-01 DOI: 10.1016/j.jve.2024.100434
M. Nühn, N. Sabet, K. Van Abeelen, P. Schipper, A. Basson, A. Wensing, L. De Witte, M. Papathanasopoulos, M. Nijhuis, J. Symons, Justine T. Blonk, Nanouk Zuidmeer
{"title":"7.5 – 00009 Postmortem analyses of the central nervous system in individuals with HIV demonstrate that infection of microglia contributes to inflammatory pathways despite viral suppression","authors":"M. Nühn,&nbsp;N. Sabet,&nbsp;K. Van Abeelen,&nbsp;P. Schipper,&nbsp;A. Basson,&nbsp;A. Wensing,&nbsp;L. De Witte,&nbsp;M. Papathanasopoulos,&nbsp;M. Nijhuis,&nbsp;J. Symons,&nbsp;Justine T. Blonk,&nbsp;Nanouk Zuidmeer","doi":"10.1016/j.jve.2024.100434","DOIUrl":"10.1016/j.jve.2024.100434","url":null,"abstract":"","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"10 ","pages":"Pages 27-28"},"PeriodicalIF":3.5,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143181178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ST2.2 – 00065 Models and correlates of intact and defective HIV DNA decay in Kenyan children over 8 years of ART 接受抗逆转录病毒治疗8年的肯尼亚儿童中完整和有缺陷的HIV DNA衰变的模型和相关因素
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2024-12-01 DOI: 10.1016/j.jve.2024.100447
D. Reeves, M. Litchford, C. Fish, A. Farrell-Sherman, N. Ahmed, M. Poindexter, N. Cassidy, J. Neary, D. Wamalwa, A. Langat, D. Chebet, H. Moraa, J. Slyker, S. Benki-Nugent, L. Cohn, J. Schiffer, J. Overbaugh, G. John-Stewart, D. Lehman
{"title":"ST2.2 – 00065 Models and correlates of intact and defective HIV DNA decay in Kenyan children over 8 years of ART","authors":"D. Reeves,&nbsp;M. Litchford,&nbsp;C. Fish,&nbsp;A. Farrell-Sherman,&nbsp;N. Ahmed,&nbsp;M. Poindexter,&nbsp;N. Cassidy,&nbsp;J. Neary,&nbsp;D. Wamalwa,&nbsp;A. Langat,&nbsp;D. Chebet,&nbsp;H. Moraa,&nbsp;J. Slyker,&nbsp;S. Benki-Nugent,&nbsp;L. Cohn,&nbsp;J. Schiffer,&nbsp;J. Overbaugh,&nbsp;G. John-Stewart,&nbsp;D. Lehman","doi":"10.1016/j.jve.2024.100447","DOIUrl":"10.1016/j.jve.2024.100447","url":null,"abstract":"","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"10 ","pages":"Page 36"},"PeriodicalIF":3.5,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143181215","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
PP2.6 – 00048 The HIV reservoir can be established in either quiescent or senescent CD4 T cells HIV病毒库可以在静止或衰老的CD4 T细胞中建立
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2024-12-01 DOI: 10.1016/j.jve.2024.100476
R. Matus Nicodemos, D. Ambrozak, D. Douek, R. Koup
{"title":"PP2.6 – 00048 The HIV reservoir can be established in either quiescent or senescent CD4 T cells","authors":"R. Matus Nicodemos,&nbsp;D. Ambrozak,&nbsp;D. Douek,&nbsp;R. Koup","doi":"10.1016/j.jve.2024.100476","DOIUrl":"10.1016/j.jve.2024.100476","url":null,"abstract":"","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"10 ","pages":"Pages 56-57"},"PeriodicalIF":3.5,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143181421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
PP2.11 – 00011 The cellular factors BRD4 and HSF1 are critical initiators of P-TEFbdependent HIV-1 latency reversal in primary T cells 细胞因子BRD4和HSF1是原代T细胞中p - tef2依赖性HIV-1潜伏期逆转的关键启动因子
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2024-12-01 DOI: 10.1016/j.jve.2024.100481
M. Yang, U. Mbonye, S. Wu, C.M. Chang, J. Karn
{"title":"PP2.11 – 00011 The cellular factors BRD4 and HSF1 are critical initiators of P-TEFbdependent HIV-1 latency reversal in primary T cells","authors":"M. Yang,&nbsp;U. Mbonye,&nbsp;S. Wu,&nbsp;C.M. Chang,&nbsp;J. Karn","doi":"10.1016/j.jve.2024.100481","DOIUrl":"10.1016/j.jve.2024.100481","url":null,"abstract":"","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"10 ","pages":"Page 59"},"PeriodicalIF":3.5,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143134580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
2.1 – 00040 Lenacapavir impairs gag proteins expression by HIV-infected cells Lenacapavir损害hiv感染细胞gag蛋白的表达
IF 3.5 4区 医学
Journal of Virus Eradication Pub Date : 2024-12-01 DOI: 10.1016/j.jve.2024.100400
C. Faua, S. Bernacchi, A. Ursenbach, M. Negroni, P. Gantner
{"title":"2.1 – 00040 Lenacapavir impairs gag proteins expression by HIV-infected cells","authors":"C. Faua,&nbsp;S. Bernacchi,&nbsp;A. Ursenbach,&nbsp;M. Negroni,&nbsp;P. Gantner","doi":"10.1016/j.jve.2024.100400","DOIUrl":"10.1016/j.jve.2024.100400","url":null,"abstract":"","PeriodicalId":17552,"journal":{"name":"Journal of Virus Eradication","volume":"10 ","pages":"Page 4"},"PeriodicalIF":3.5,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143176156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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