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营养途径和类型会影响对细菌性肺炎的黏膜免疫。

Route and type of nutrition influence mucosal immunity to bacterial pneumonia.

作者信息

King B K, Kudsk K A, Li J, Wu Y, Renegar K B

机构信息

Department of Surgery, The University of Tennessee, Memphis, USA.

出版信息

Ann Surg. 1999 Feb;229(2):272-8. doi: 10.1097/00000658-199902000-00016.

Abstract

OBJECTIVE

To develop a model of established respiratory immunity against Pseudomonas aeruginosa pneumonia and to investigate the effects of route and type of nutrition on this immunity.

SUMMARY BACKGROUND DATA

Diet influences the ability of gut-associated lymphoid tissue (GALT) to maintain mucosal immunity. Complex enteral diets and chow maintain normal GALT populations against established IgA-mediated antiviral respiratory immunity. Both intravenous and intragastric total parenteral nutrition (TPN) produce GALT atrophy, but only intragastric TPN preserves established antiviral immunity. The authors hypothesized that both GALT-depleting diets (intragastric and intravenous TPN) would impair immunity against bacterial pneumonia.

METHODS

P. aeruginosa was administered intratracheally to determine the mortality rate at increasing doses, and liposomes containing P. aeruginosa antigens were used to generate effective respiratory immunization. In the final experiment, mice received liposomes containing P. aeruginosa antigens to establish immunity and then were randomized to chow, complex enteral diets, intragastric TPN, or intravenous TPN. After 5 days of diet, mice received live intratracheal P. aeruginosa, and the death rate was recorded at 24 and 48 hours.

RESULTS

The LD50 and LD100 were 9 x 10(7) and 12 x 10(7), respectively. Immunization reduced the mortality rate from 66% to 12%. This immunization was maintained in mice fed chow or a complex enteral diet and was lost in animals receiving intravenous TPN. Intragastric TPN partially preserved this respiratory immunity.

CONCLUSIONS

Protection against bacterial pneumonia can be induced by prior antigenic immunization. This protection is lost with intravenous TPN, partially preserved with a chemically defined enteral diet, and completely preserved with chow or complex enteral diets. Both route and type of nutrition influence antibacterial respiratory tract immunity.

摘要

目的

建立针对铜绿假单胞菌肺炎的成熟呼吸道免疫模型,并研究营养途径和类型对该免疫的影响。

总结背景数据

饮食会影响肠道相关淋巴组织(GALT)维持黏膜免疫的能力。复合肠内饮食和普通食物可维持正常的GALT群体,以对抗已建立的IgA介导的抗病毒呼吸道免疫。静脉内和胃内全胃肠外营养(TPN)都会导致GALT萎缩,但只有胃内TPN能保留已建立的抗病毒免疫。作者推测,两种消耗GALT的饮食(胃内和静脉内TPN)都会损害针对细菌性肺炎的免疫力。

方法

经气管内给予铜绿假单胞菌以确定不同剂量下的死亡率,并使用含有铜绿假单胞菌抗原的脂质体进行有效的呼吸道免疫。在最终实验中,小鼠接受含有铜绿假单胞菌抗原的脂质体以建立免疫,然后随机分为普通食物组、复合肠内饮食组、胃内TPN组或静脉内TPN组。饮食5天后,小鼠经气管内接种活的铜绿假单胞菌,并记录24小时和48小时时的死亡率。

结果

半数致死量(LD50)和绝对致死量(LD100)分别为9×10⁷和12×10⁷。免疫使死亡率从66%降至12%。这种免疫在喂食普通食物或复合肠内饮食的小鼠中得以维持,而在接受静脉内TPN的动物中则消失。胃内TPN部分保留了这种呼吸道免疫。

结论

预先进行抗原免疫可诱导对细菌性肺炎的保护作用。这种保护作用在静脉内TPN时丧失,在化学定义的肠内饮食时部分保留,在普通食物或复合肠内饮食时完全保留。营养途径和类型都会影响呼吸道抗菌免疫。

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