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自然感染和接种疫苗对支原体引起的呼吸道疾病的保护作用。

Protection by natural infection and vaccination against respiratory diseases caused by mycoplasmas.

作者信息

Whittlestone P

出版信息

Dev Biol Stand. 1975;28:571-85.

PMID:805075
Abstract

Following recovery from mycoplasmal respiratory disease animals are resistant to reinfection. The mechanism of this immunity is not well understood; usually there is poor correlation between circulating antibody levels and the degree of resistance to reinfection, but more work is needed to both man and animals on the significance of the different classes and types of circulating antibody. Because mycoplasmal infection of the respiratory tract is largely confined to the epithelial surface, it seems likely that local immunity will prove to be important. The levels of specific immunoglobulins, particularly IgA, in respiratory tract secretions may be related to immunity. It is probably, however, that cell-mediated immunity is the main determinant of resistance to mycoplasmal respiratory disease: firstly, there is evidence in several diseases that lymphocytes can be transformed by mycoplasmal antigen and there are some indications thatthe degree of this cell-mediated immunity might correlate with resistance to infection; secondly, antigen has produced skin reactions indicative of delayed hypersensitivity in some mycoplasmal diseases. Vaccination with inactivated vaccines has not produced satisfactory immunity; attenuated mycoplasma strains or temperature-sensitive mutants seem more likely to afford adequate protection against respiratory diseases caused by mycoplasmas.

摘要

从支原体呼吸道疾病恢复后,动物对再次感染具有抵抗力。这种免疫机制尚未完全了解;通常,循环抗体水平与再次感染的抵抗程度之间相关性较差,但对于人和动物循环抗体的不同类别和类型的意义仍需开展更多研究。由于呼吸道支原体感染主要局限于上皮表面,局部免疫似乎可能很重要。呼吸道分泌物中特异性免疫球蛋白的水平,尤其是IgA,可能与免疫有关。然而,细胞介导的免疫可能是抵抗支原体呼吸道疾病的主要决定因素:首先,在几种疾病中有证据表明淋巴细胞可被支原体抗原转化,并且有一些迹象表明这种细胞介导免疫的程度可能与抗感染能力相关;其次,在一些支原体疾病中,抗原已产生表明迟发型超敏反应的皮肤反应。用灭活疫苗进行接种未产生令人满意的免疫力;减毒支原体菌株或温度敏感突变体似乎更有可能为支原体引起的呼吸道疾病提供充分保护。

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