融合表達ESAT6-CFP10結核病疫苗的構建及其免疫學特性研究
發(fā)布時間:2018-12-13 04:05
【摘要】:結核病(Tuberculosis,TB)是由結核分枝桿菌(Mycobacterium tuberculosis,MTB)所致以呼吸系統(tǒng)感染為主的慢性傳染病,據(jù)WHO估計,目前全世界約有1/3人口感染MTB,每年有1000萬新發(fā)患者和300萬患者死亡。貧窮、人口增加、流動人口增多、耐藥MTB增多及艾滋病流行等使TB問題雪上加霜。我國是全球22個TB高負擔國家之一,現(xiàn)有MTB感染人數(shù)已達4億,傳染性TB患者達到200萬?ń槊(BCG)雖被廣泛用于預防TB,但其效果仍不夠滿意。研究認為BCG可預防并減輕兒童的嚴重TB,但對成人TB的預防作用從0到80%不等。導致此現(xiàn)象的原因在于BCG菌株的變異使保護性抗原丟失、人群間遺傳或營養(yǎng)的差異及環(huán)境等因素的影響。鑒于BCG自身的不足,以及當前TB流行的嚴重性,研究新的疫苗用于TB的預防已成為當前國內(nèi)外研究熱點。 MTB早期培養(yǎng)濾液蛋白(CFP)中的ESAT6和CFP10是重要的保護性抗原。本研究先后構建了融合表達ESAT6和CFP10蛋白的亞單位疫苗、基因疫苗以及重組恥垢分枝桿菌(mycobacterium smegmatis,M.S)疫苗,并比較了各自誘發(fā)的細胞免疫應答水平和對感染小鼠的保護力,
[Abstract]:Tuberculosis (Tuberculosis,TB) is a chronic infectious disease mainly caused by respiratory infection caused by Mycobacterium tuberculosis (Mycobacterium tuberculosis,MTB). According to WHO estimates, about one-third of the world's population is infected with MTB,. 10 million new cases and 3 million deaths occur every year. Poverty, population growth, increased floating population, increased drug-resistant MTB and the AIDS epidemic make the TB problem worse. China is one of the 22 countries with high burden of TB in the world. The number of people infected with MTB has reached 400 million and the number of patients with infectious TB has reached 2 million. BCG (BCG) is widely used to prevent TB, but its effect is not satisfactory. The study suggests that BCG can prevent and reduce severe TB, in children, but the preventive effect on adult TB varies from 0 to 80%. The causes of this phenomenon are the loss of protective antigen due to the variation of BCG strains, the genetic or nutritional differences among populations and the influence of environmental factors. In view of the deficiency of BCG itself and the severity of the current TB epidemic, the research on the application of new vaccines to the prevention of TB has become a hot research topic at home and abroad. ESAT6 and CFP10 in MTB early culture filtrate protein (CFP) are important protective antigens. In this study, subunit vaccines, gene vaccines and recombinant Mycobacterium smegmatis (mycobacterium smegmatis,M.S) vaccines expressing ESAT6 and CFP10 proteins were constructed successively, and the cellular immune response levels and the protective effects on infected mice were compared.
【學位授予單位】:第四軍醫(yī)大學
【學位級別】:博士
【學位授予年份】:2005
【分類號】:R392
本文編號:2375840
[Abstract]:Tuberculosis (Tuberculosis,TB) is a chronic infectious disease mainly caused by respiratory infection caused by Mycobacterium tuberculosis (Mycobacterium tuberculosis,MTB). According to WHO estimates, about one-third of the world's population is infected with MTB,. 10 million new cases and 3 million deaths occur every year. Poverty, population growth, increased floating population, increased drug-resistant MTB and the AIDS epidemic make the TB problem worse. China is one of the 22 countries with high burden of TB in the world. The number of people infected with MTB has reached 400 million and the number of patients with infectious TB has reached 2 million. BCG (BCG) is widely used to prevent TB, but its effect is not satisfactory. The study suggests that BCG can prevent and reduce severe TB, in children, but the preventive effect on adult TB varies from 0 to 80%. The causes of this phenomenon are the loss of protective antigen due to the variation of BCG strains, the genetic or nutritional differences among populations and the influence of environmental factors. In view of the deficiency of BCG itself and the severity of the current TB epidemic, the research on the application of new vaccines to the prevention of TB has become a hot research topic at home and abroad. ESAT6 and CFP10 in MTB early culture filtrate protein (CFP) are important protective antigens. In this study, subunit vaccines, gene vaccines and recombinant Mycobacterium smegmatis (mycobacterium smegmatis,M.S) vaccines expressing ESAT6 and CFP10 proteins were constructed successively, and the cellular immune response levels and the protective effects on infected mice were compared.
【學位授予單位】:第四軍醫(yī)大學
【學位級別】:博士
【學位授予年份】:2005
【分類號】:R392
【引證文獻】
相關期刊論文 前1條
1 謝婷;李文桂;;結核分枝桿菌CFP10疫苗研究進展[J];中國病原生物學雜志;2007年03期
相關博士學位論文 前1條
1 簡文;屋塵螨抗原Der p2重組恥垢分枝桿菌口服疫苗的制備及其實驗研究[D];第四軍醫(yī)大學;2008年
相關碩士學位論文 前1條
1 謝婷;結核分枝桿菌重組Bb-ESAT-6-MPT64疫苗保護力及其免疫機制研究[D];重慶醫(yī)科大學;2008年
,本文編號:2375840
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