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社区获得性肺炎不同病因患者细胞因子/趋化因子的演变。

Evolution of cytokines/chemokines in cases with community-acquired pneumonia and distinct etiologies.

机构信息

Bahiana School of Medicine and Public Health, Bahiana Foundation for Science Development, Salvador, Brazil.

Instituto Gonçalo Moniz, Fundação Oswaldo Cruz-Fiocruz, Salvador, Brazil.

出版信息

Pediatr Pulmonol. 2020 Jan;55(1):169-176. doi: 10.1002/ppul.24533. Epub 2019 Sep 25.

Abstract

AIM

To compare the systemic cytokines/chemokines levels over time during the evolution of children hospitalized with community-acquired pneumonia (CAP) with and without pneumococcal infection.

METHODS

Children less than 5-years-old hospitalized with CAP were prospectively investigated in Salvador, Brazil. Clinical data and biological samples were collected to investigate 20 etiological agents and to determine serum cytokines/chemokines levels on admission and 2 to 4 weeks later. Cases with pneumococcal infection received this diagnosis irrespective of also having other etiologies.

RESULTS

A total of 277 patients were enrolled, however, serum sample was unavailable for cytokine measurement upon admission (n = 61) or upon follow-up visit (n = 36), etiology was undetected (n = 50) and one patient did not attend the follow-up visit. Therefore, this study group comprised of 129 cases with established etiology. The median (interquartile range) age and sampling interval was 18 (9-27) months and 18 (16-21) days, respectively. Established etiology was viral (52.0%), viral-bacterial (30.2%), and bacterial (17.8%). Pneumococcal infection was found in 31 (24.0%) patients. Overall, median interleukin-6 (IL-6; 10.6 [4.7-30.6] vs 21.0 [20.2-21.7]; P = .03), IL-10 (3.5 [3.1-4.5] vs 20.1 [19.8-20.4]; P < .001), and CCL2 (19.3 [12.4-23.2] vs 94.0 [67.2-117.8]; P < .001) were significantly higher in convalescent serum samples, whereas median CXCL10 (83.6 [36.4-182.9] vs 14.6 [0-116.6]; P < .001) was lower. Acute vs convalescent levels evolution of IL-10, CCL2, and CXCL10 did not differ among patients with or without pneumococcal infection. However, IL-6 decreased (27.8 [12.3-48.6] vs 20.8 [20.2-22.6]; P = .1) in patients with pneumococcal infection and increased (9.0 [4.2-22.6] vs 21.0 [20.2-21.7]; P = .001) in patients without it.

CONCLUSION

The marked increase of IL-6 serum levels during the acute phase makes it a potential biomarker of pneumococcal infection among children with CAP.

摘要

目的

比较伴有和不伴有肺炎链球菌感染的社区获得性肺炎(CAP)住院患儿在病程中系统性细胞因子/趋化因子水平的变化。

方法

本前瞻性研究在巴西萨尔瓦多对小于 5 岁因 CAP 住院的患儿进行调查。采集临床数据和生物样本,以调查 20 种病因,并在入院时和 2 至 4 周后测定血清细胞因子/趋化因子水平。有肺炎链球菌感染的病例不论是否同时存在其他病因,均做出此诊断。

结果

共纳入 277 例患儿,然而,入院时(n=61)或随访时(n=36)细胞因子检测的血清样本不可用,病因未检出(n=50),1 例患儿未参加随访。因此,本研究组纳入了 129 例病因明确的病例。中位(四分位距)年龄和采样间隔分别为 18(9-27)个月和 18(16-21)天。明确的病因是病毒(52.0%)、病毒-细菌(30.2%)和细菌(17.8%)。31 例(24.0%)患儿有肺炎链球菌感染。总体而言,入院时,白细胞介素 6(IL-6;10.6[4.7-30.6] vs 21.0[20.2-21.7];P=0.03)、IL-10(3.5[3.1-4.5] vs 20.1[19.8-20.4];P<0.001)和 CCL2(19.3[12.4-23.2] vs 94.0[67.2-117.8];P<0.001)明显更高,而 CXCL10 中位水平(83.6[36.4-182.9] vs 14.6[0-116.6];P<0.001)更低。有或没有肺炎链球菌感染的患儿的急性 vs 恢复期的 IL-10、CCL2 和 CXCL10 水平演变没有差异。然而,肺炎链球菌感染患儿的 IL-6 下降(27.8[12.3-48.6] vs 20.8[20.2-22.6];P=0.1),而无肺炎链球菌感染患儿的 IL-6 升高(9.0[4.2-22.6] vs 21.0[20.2-21.7];P=0.001)。

结论

在 CAP 住院患儿中,IL-6 血清水平在急性期的显著升高使其成为肺炎链球菌感染的潜在生物标志物。

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