Abstract
洪翔,于红,王蓓.新生儿B族链球菌感染相关疾病影响因素的研究进展[J].Chinese journal of Epidemiology,2018,39(2):249-252
新生儿B族链球菌感染相关疾病影响因素的研究进展
Progress on influencing factors regarding the neonatal group B streptococcal infectious diseases
Received:July 20, 2017  
DOI:10.3760/cma.j.issn.0254-6450.2018.02.022
KeyWord: B族链球菌  新生儿  感染  影响因素
English Key Word: Group B streptococcus  Neonatal  Infection  Risk factor
FundProject:高等学校博士学科点专项科研基金(20130092110048)
Author NameAffiliationE-mail
Hong Xiang Department of Epidemiology and Health Statistics, School of Public Health, Southeast University
Key Laboratory of Environmental Medicine Engineering of Ministry of Education, Nanjing 210009, China 
 
Yu Hong Department of Obstetrics, Southeast University Affiliated Zhongda Hospital, Nanjing 210009, China  
Wang Bei Department of Epidemiology and Health Statistics, School of Public Health, Southeast University
Key Laboratory of Environmental Medicine Engineering of Ministry of Education, Nanjing 210009, China 
wangbeilxb@seu.edu.cn 
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Abstract:
      B族链球菌(GBS)是围产期严重感染性疾病的主要致病菌之一。新生儿感染GBS可能导致肺炎、败血症、脑膜炎等严重疾病,甚至引起死亡。有约1%~2% GBS感染的新生儿会发展成为GBS相关疾病,其发病的影响因素值得探索。鉴于国内尚缺乏针对GBS感染及发病机制的深入研究,本文全面阐述可能与新生儿GBS相关疾病发生有关的因素,包括妊娠相关因素(孕妇生殖道GBS定植、早产、胎膜早破等)、病原体因素(细菌菌株、载量、毒力等)、宿主免疫水平(炎症因子以及抗细胞因子"自身抗体"等)以及宿主基因缺陷引起的新生儿免疫缺陷等。
English Abstract:
      Group B streptococcus (GBS) is one of the severe pathogenic bacteria during the perinatal period, both on pregnant women and newborns. GBS infection may lead to pneumonia, septicemia, meningitis or other severe disease, even death in neonates. Although only 1%-2% infections will develop into GBS disease among the neonates, the etiological mechanism of which is worth researching. This review summarizes the possible factors related to GBS infection or occurrence of the disease, including the risk in gestation period (for example, colonization of GBS on vagina of pregnant women, preterm birth or premature rupture of fetal membranes and so on), related pathogens (bacteria strains, loads or virulence), immune level (inflammatory factor or neutralizing anticytokine auto-Abs), gene defect or primary immunodeficiencies of the hosts.
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