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首页> 外文期刊>Infection and immunity >Dietary protein deficiency and Mycobacterium bovis BCG affect interleukin-2 activity in experimental pulmonary tuberculosis.
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Dietary protein deficiency and Mycobacterium bovis BCG affect interleukin-2 activity in experimental pulmonary tuberculosis.

机译:饮食中的蛋白质缺乏和牛分枝杆菌BCG影响实验性肺结核中白细胞介素2的活性。

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Inbred strain 2 guinea pigs were vaccinated with Mycobacterium bovis BCG or were left unvaccinated. They were maintained for 6 weeks on defined, isocaloric diets containing either 30% (control animals) or 10% (animals receiving low protein) ovalbumin as the sole protein source. Animals were challenged by the respiratory route with a low dose of virulent M. tuberculosis H37Rv and killed 4 weeks later. Protein-malnourished animals were not protected by previous vaccination with BCG. Lymphocytes isolated from various tissues were tested in vitro for proliferative responses to mitogen (concanavalin A) and antigen (purified protein derivative [PPD]), production of interleukin-2 (IL-2), and response to exogenous recombinant IL-2 (rIL-2). Protein-malnourished guinea pigs responded only weakly to PPD skin tests, and their blood and lymph node lymphocytes exhibited impaired proliferation when cultured with PPD in vitro. IL-2 levels were consistently low in cultures of stimulated blood and spleen lymphocytes from protein-deprived animals. BCG vaccination of nutritionally normal guinea pigs, on the other hand, induced significantly more IL-2 production by PPD- and concanavalin A-stimulated lymphocytes. The addition of exogenous mouse rIL-2 (40 and 80 U/ml) in vitro to PPD-stimulated blood and lymph node cells from nonvaccinated, protein-deprived guinea pigs resulted in no improvement of the proliferative response. Previous vaccination of malnourished guinea pigs did not consistently enhance the response of PPD-stimulated lymphocytes to added rIL-2. Dietary protein deficiency and BCG vaccination appear to modulate antigen-driven cellular immunity in animals with tuberculosis by altering the production of, and the response to, IL-2 by PPD-stimulated lymphocytes.
机译:将近交品系2豚鼠接种牛分枝杆菌BCG或不接种。将它们按限定的等热量饮食维持6周,这些饮食含有30%(对照动物)或10%(动物接受低蛋白)卵清蛋白作为唯一的蛋白质来源。用低剂量的强力结核分枝杆菌H37Rv通过呼吸道攻击动物,并在4周后将其杀死。蛋白质营养不良的动物未接受过先前接种BCG的疫苗的保护。体外测试了从各种组织分离的淋巴细胞对促分裂原(伴刀豆球蛋白A)和抗原(纯化的蛋白衍生物[PPD])的增殖反应,白介素2(IL-2)的产生以及对外源重组IL-2(rIL)的反应-2)。营养不良的豚鼠对PPD皮肤试验的反应较弱,并且在体外培养PPD时其血液和淋巴结淋巴细胞的增殖受损。在缺乏蛋白质的动物的刺激血液和脾淋巴细胞培养物中,IL-2水平始终较低。另一方面,对营养正常的豚鼠进行卡介苗接种可明显诱导PPD和伴刀豆球蛋白A刺激的淋巴细胞产生更多的IL-2。从未经疫苗接种,蛋白质剥夺的豚鼠向PPD刺激的血液和淋巴结细胞中添加外源小鼠rIL-2(40和80 U / ml)在体外未导致增殖反应的改善。营养不良的豚鼠先前的疫苗接种不能始终如一地增强PPD刺激的淋巴细胞对添加的rIL-2的反应。饮食中的蛋白质缺乏和BCG疫苗接种似乎通过改变PPD刺激的淋巴细胞对IL-2的产生和应答,来调节结核病动物的抗原驱动的细胞免疫。

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