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结核疫苗的研究进展 被引量:1

search progress of mycobacterium tuberculosis and vaccina
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摘要 结核病是由结核分枝杆菌引发的一种传染病。1882年,结核分枝杆菌(mycobacterium tuberculosis,Mtb)由Rober t Koch发现,至今仍是致人类死亡主要病原体之一。更可怕是,多重耐药(MDR)和广泛耐药(XDR)Mtb患病率的明显增加。上世纪90年代,世界卫生组织(World Health Organization,WHO)宣布结核病处于全球性紧急状态。结核病的最佳预防措施是接种疫苗,但是卡介苗(bacille Calmette-Guér in,BCG)对成人的保护效力不完全。随着Mtb基因序列的检测成功,疫苗的研究取得了重大的进展,已经有十几种候选疫苗准备或已进人体临床试验阶段。当前热门的候选疫苗包括重组BCG疫苗、减毒Mtb活疫苗和亚单位疫苗等。本文将从这些方面进行综述。 Tuberculosis is a kind of epidemic disease caused by the bacterium mycobacterium tuberculosis(Mtb).Mtb was discovered by Robert Koch in 1882,remains a leading cause of mortality worldwide.What is more,the morbidity of MDR and XDR Mtb is increasing.Tuberculosis is a global emergency announced by The World Health Organization(WHO) in last 90 s.The best prevention is receiving vaccine,but Mycobacterium bovis bacille Calmette-Guerin(BCG) does not have a whole protective effect in adults.After the M.tuberculosis genome was published,great improvements are attained as several vaccine candidates are in the clinical trial process,such as recombinant BCGs,subunit vaccines.This article will do a review concerning these respects.
出处 《临床与病理杂志》 2016年第1期85-88,共4页 Journal of Clinical and Pathological Research
关键词 结核病 疫苗 卡介苗 tuberculosis vaccine bacille Calmette-Guerin(BCG
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  • 1Novoa-Aponte L, Soto Ospina CY. Mycobacterium tuberculosis P-type ATPases: possible targets for drug or vaccine development[J]. Biomed Res Int, 2014, 2014: 296986.
  • 2Junqueira-Kipnis AP, Marques Nero LM, Kipnis A. Role of Fused Mycobacterium tuberculosis Immunogens and Adjuvants in Modern Tuberculosis Vaccines[J]. Front Immunol, 2014, 5: 188.
  • 3Elkabani M, Greene JN, Vincent AL, et al. Disseminated Mycobacterium bovis after intravesicular bacillus calmette-Gu rin treatments for bladder cancer[J]. Cancer Control, 2000, 7(5): 476-481.
  • 4Sixsmith JD, Panas MW, Lee S, et al. Recombinant Mycobacterium boris bacillus Calmette-Gu6rin vectors prime for strong cellular responses to simian immunodeficiency virus gag in rhesus macaques [J]. Clin Vaccine Immtmol, 2014, 21(10): 1385-1395.
  • 5Orme IM. Tuberculosis vaccine types and timings[J]. Clin Vaccine Immunol, 2015, 22(3): 249-257.
  • 6Daginawala HF, Warke SR, Kalorey DR, et al. Investigation of Immune Biomarkers Using Subcutaneous Model of M. tuberculosis Infection in BALB/c Mice: A Preliminary Report[J]. Immune Netw, 2015, 15(2): 83-90.
  • 7Cayabyab MJ, Macovei L, Campos-Neto A. Current and novel approaches to vaccine development against tuberculosis[J]. Front Cell Infect Microbiol, 2012, 2: 154.
  • 8van DisselJT, Soonawala D, Joosten SA, et al. Ag85B-ESAT-6 adjuvanted with IC31 promotes strong and long-lived Mycobacterium tuberculosis specific T cell responses in volunteers with previous BCG vaccination or tuberculosis infection [J]. Vaccine, 2011, 29(11): 2100-2109.
  • 9Sun R, Skeiky YA, Izzo A, et al. Novel recombinant BCG expressing perfringolysin O and the over-expression of key immunodominantantigens; pre-dinical characterization, safety and protection against challenge with Mycobacterium tuberculosis[J]. Vaccine, 2009, 27(33): 4412-4423.
  • 10Desel C, Dorhoi A, Bandermann S, et al. Recombinant BCG AureC hly+ induces superior protection over parental BCG by stimulating a balanced combination of type 1 and type 17 cytokine responses[J].J Infect Dis, 2011,204(10): 1573-1584.

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