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用细菌多糖和佐剂进行口服免疫可增强抗原特异性肺分泌抗体反应及对肺炎的抵抗力。

Oral immunization with bacterial polysaccharide and adjuvant enhances antigen-specific pulmonary secretory antibody response and resistance to pneumonia.

作者信息

Abraham E, Robinson A

机构信息

Department of Medicine, UCLA Medical Center 90024.

出版信息

Vaccine. 1991 Oct;9(10):757-64. doi: 10.1016/0264-410x(91)90293-f.

Abstract

Nosocomial pneumonia, often due to Pseudomonas aeruginosa, occurs frequently after haemorrhage and trauma, and contributes to the increased incidence of morbidity and mortality in this clinical setting. In order to determine if enhancement of bacterial antigen-specific secretory IgA (sIgA) titres in the lungs can increase resistance to P. aeruginosa pneumonia following haemorrhage, we investigated oral immunization strategies, using bacterial polysaccharides (levan, from Aerobacter levanicum, and P. aeruginosa polysaccharide type I) and adjuvant (cholera toxin and the B-subunit of cholera toxin), capable of increasing bacterial polysaccharide-specific pulmonary secretory antibody titres. Oral co-administration of 1000 micrograms levan and 10 micrograms cholera toxin resulted in increased titres of levan-specific sIgA in lung lavages and increased numbers of levan-specific pulmonary plasma cells, but no changes in serum anti-levan titres. Similarly, oral co-administration of 1000 micrograms P. aeruginosa polysaccharide and 10 micrograms cholera toxin produced increased anti-P. aeruginosa polysaccharide titres in lung lavages. Significant decreases in anti-levan pulmonary sIgA titres and in numbers of levan-specific pulmonary plasma cells were found when oral immunization with levan and cholera toxin was performed 4 days following haemorrhage, but not if the mice were immunized 8 h after blood loss. Although haemorrhage markedly increased the susceptibility of mice to P. aeruginosa pneumonia, significant protection from mortality could be achieved through oral immunization with 1000 micrograms P. aeruginosa polysaccharide and 10 micrograms cholera toxin 8 h after haemorrhage. These results demonstrate that haemorrhage induces marked alterations in bacterial antigen-specific pulmonary B-cell responses, which contribute to the increased susceptibility to infection in this setting.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

医院获得性肺炎常由铜绿假单胞菌引起,在出血和创伤后频繁发生,并导致该临床环境中发病率和死亡率的增加。为了确定增强肺部细菌抗原特异性分泌型IgA(sIgA)滴度是否能增加出血后对铜绿假单胞菌肺炎的抵抗力,我们研究了口服免疫策略,使用细菌多糖(来自左旋糖酐气杆菌的果聚糖和I型铜绿假单胞菌多糖)和佐剂(霍乱毒素和霍乱毒素B亚基),它们能够增加细菌多糖特异性肺分泌抗体滴度。口服1000微克果聚糖和10微克霍乱毒素导致肺灌洗中果聚糖特异性sIgA滴度增加以及果聚糖特异性肺浆细胞数量增加,但血清抗果聚糖滴度无变化。同样,口服1000微克铜绿假单胞菌多糖和10微克霍乱毒素可使肺灌洗中抗铜绿假单胞菌多糖滴度增加。出血后4天进行果聚糖和霍乱毒素口服免疫时,发现抗果聚糖肺sIgA滴度和果聚糖特异性肺浆细胞数量显著降低,但在失血后8小时对小鼠进行免疫则未出现这种情况。尽管出血显著增加了小鼠对铜绿假单胞菌肺炎的易感性,但在出血后8小时口服1000微克铜绿假单胞菌多糖和10微克霍乱毒素可显著降低死亡率。这些结果表明,出血诱导细菌抗原特异性肺B细胞反应发生显著改变,这导致了在此环境中对感染易感性的增加。(摘要截短至250字)

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