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1.400038 重庆,陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心
2.154007 黑龙江 佳木斯,佳木斯大学临床医学院
[李海波, E-mail: lihaibo@tmmu.edu.cnLI Haibo, E-mail: lihaibo@tmmu.edu.cn
收稿:2024-01-14,
修回:2024-01-29,
纸质出版:2024-04-30
移动端阅览
程浩, 杨赟, 孙红武, 等. TLR2/TLR9激动剂对鲍曼不动杆菌肺部感染的保护作用[J]. 陆军军医大学学报, 2024,46(8):829-836.
Hao CHENG, Yun YANG, Hongwu SUN, et al. Protective effect of TLR2/TLR9 agonists on pulmonary
程浩, 杨赟, 孙红武, 等. TLR2/TLR9激动剂对鲍曼不动杆菌肺部感染的保护作用[J]. 陆军军医大学学报, 2024,46(8):829-836. DOI: 10.16016/j.2097-0927.202401052.
Hao CHENG, Yun YANG, Hongwu SUN, et al. Protective effect of TLR2/TLR9 agonists on pulmonary
目的
2
评价toll-like receptor(TLR)2/TLR9激动剂对肺部感染鲍曼不动杆菌(
Acinetobacter baumannii
Ab)小鼠的保护作用。
方法
2
将6~8周龄雌性C57小鼠分为PBS组、Pam
2
CSK
4
(Pam)组、CpG ODN(CpG)组和Pam+CpG组,以不同剂量滴鼻免疫后24 h进行Ab肺部致死性感染,观察小鼠生存率。构建亚致死剂量Ab肺部感染模型,测定感染后小鼠血液、肺脏、肝脏、肾脏和脾脏的细菌定植量,并取小鼠肺脏和肾脏进行HE染色,分析病理损伤程度。探索免疫1、3、7 d后对小鼠Ab感染的保护作用,明确保护时间窗。Pam+ CpG体外刺激A549上皮细胞和RAW264.7细胞,考察两种细胞对Ab的杀伤或吞噬作用。
结果
2
与PBS组比较,Pam+CpG组能显著提高Ab致死感染小鼠的生存率(
P
<
0.05,
P
<
0.01),降低亚致死感染后小鼠血液(
P
<
0.01)、肺脏(
P
<
0.01)、肝脏(
P
<
0.05)、肾脏(
P
<
0.01)和脾脏(
P
<
0.01)的细菌定植量,减轻感染导致的病理损伤;在感染之前1 d或3 d免疫均可显著提高小鼠的生存率(
P
<
0.05),其中免疫后3 d保护效果最好。与PBS、Pam、CpG组比较,Pam+CpG组可以显著促进A549上皮细胞和R AW264.7细胞对Ab的杀伤或吞噬作用(
P
<
0.01)。
结论
2
TLR2/TLR9激动剂合用对Ab致死和亚致死感染均具有显著的保护作用,可能的机制是其促进了肺上皮细胞和巨噬细胞对Ab的杀伤或吞噬作用。
Objective
2
To investigate the protective effect of Tol
l-like receptor (TLR) 2 /TLR9 agonists
Pam
2
CSK
4
(Pam) and CpG ODN (CpG) on mice infected with
Acinetobacter baumannii
(Ab) in the lungs.
Methods
2
Female C57 mice (6~8 weeks old) were randomly divided into PBS
Pam
CpG and Pam+CpG groups. In 24 h after intranasal immunization with different doses of the corresponding agonists
the mice were given a lethal dose of Ab infection in the lungs
and the survival rates of the mice were observed. A sublethal dose lung infection model of Ab was then established
and the bacterial colonization in the blood
lungs
liver
kidneys and spleen was measured respectively in the mice after infection. HE staining was used to observe the pathological damages in the lungs and kidneys. The protective effect of the agonists in the immunized mice against Ab was examined at 1
3 and 7 d after immunization to explore the protective time window. Pam+CpG was used to stimulate A549 cells and RAW264.7 cells to investigate the killing or phagocytic effects on Ab.
Results
2
Compared to PBS
Pam+CpG treatment significantly improved the survival rate of the mice after a lethal dose of Ab lung infection (
P
<
0.05
P
<
0.01)
reduced bacterial colonization in the blood (
P
<
0.01)
lungs (
P
<
0.01)
liver (
P
<
0.01)
kidneys (
P
<
0.01) and spleen (
P
<
0.01) in the mice after sublethal challenge
and alleviated pathological damage caused by infection. Immunization at 1 or 3 d before infection significantly improved the survival rate (
P
<
0.05)
and the protective effect was the best in 3 d after immunization. Furthermore
compared to single PBS
Pam and CpG immunization
Pam+CpG significantly promoted the killing and phagocytic effects of A549 epithelial cells and RAW264.7 cells
respectively
against Ab (
P
<
0.01).
Conclusion
2
Combined application of TLR2/TLR9 agonists exerts a significant protective effect on both lethal and sublethal infections of Ab
which might be by its promoting the killing or phagocytic effect of lung epithelial cells and macrophages against Ab.
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