{"title":"TNF-α和IFN-γ水平与急性病毒性细支气管炎严重程度的关系","authors":"Carolina Frizzera Dias, Maurício Menegatti Rigo, Daniele Cristovao Escouto, Bárbara Porto, Rita Mattiello","doi":"10.1080/08830185.2021.1889534","DOIUrl":null,"url":null,"abstract":"<p><p>Acute bronchiolitis caused by the respiratory syncytial virus triggers an inflammatory response with the production and release of several pro-inflammatory cytokines. Evidence suggests that their levels are associated with the severity of the infection. This systematic review and meta-analysis aim to assess whether the levels of TNF-α and IFN-γ are associated with the severity of acute viral bronchiolitis. We searched MEDLINE libraries (via PUBMED), EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL), Scientific Electronic Library Online (SciELO), Latin American Caribbean Health Sciences Literature (LILACS), Cumulative Index to Nursing and Allied Health Literature (CINAHL), Web of Science, and the gray literature through April 2020. Random effect models were used for general and subgroup analysis. In total, six studies were included with a total of 744 participants. The mean TNF-α levels between the severe group did not differ from the control group 0.14 (95% CI: -0.53 to 0.82, I<sup>2</sup> = 91%, <i>p</i> < 0.01); the heterogeneity was high. The results remained insignificant when the analyses were performed including only studies with high quality 0.25 (95% CI: -0.46 to 0.96, I<sup>2</sup> = 92%, <i>p</i> < 0.01) I<sup>2</sup> = 95%, <i>p</i> = 0.815), when TNF-α was nasal 0.60 (95% CI: -0.49 to 1.69), I<sup>2</sup> = 94%, <i>p</i> < 0.01), or serum -0.08 (95% CI: -0.48 to 0.31), I<sup>2</sup> = 29%, <i>p</i> = 0.24). In the analysis of studies measuring IFN-γ, there was also no significance of -0.67 (95% CI: -1.56 to 0.22, I<sup>2</sup> = 76%, <i>p</i> = 0.04). In conclusion, this meta-analysis suggests that the most severe patients do not have different mean TNF-α and IFN-γ values than patients with mild disease, but the heterogeneity of the studies was high. Supplemental data for this article is available online at https://doi.org/10.1080/08830185.2021.1889534.</p>","PeriodicalId":14333,"journal":{"name":"International Reviews of Immunology","volume":"40 6","pages":"433-440"},"PeriodicalIF":4.3000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/08830185.2021.1889534","citationCount":"3","resultStr":"{\"title\":\"Association between TNF-α and IFN-γ levels and severity of acute viral bronchiolitis.\",\"authors\":\"Carolina Frizzera Dias, Maurício Menegatti Rigo, Daniele Cristovao Escouto, Bárbara Porto, Rita Mattiello\",\"doi\":\"10.1080/08830185.2021.1889534\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Acute bronchiolitis caused by the respiratory syncytial virus triggers an inflammatory response with the production and release of several pro-inflammatory cytokines. Evidence suggests that their levels are associated with the severity of the infection. This systematic review and meta-analysis aim to assess whether the levels of TNF-α and IFN-γ are associated with the severity of acute viral bronchiolitis. We searched MEDLINE libraries (via PUBMED), EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL), Scientific Electronic Library Online (SciELO), Latin American Caribbean Health Sciences Literature (LILACS), Cumulative Index to Nursing and Allied Health Literature (CINAHL), Web of Science, and the gray literature through April 2020. Random effect models were used for general and subgroup analysis. In total, six studies were included with a total of 744 participants. The mean TNF-α levels between the severe group did not differ from the control group 0.14 (95% CI: -0.53 to 0.82, I<sup>2</sup> = 91%, <i>p</i> < 0.01); the heterogeneity was high. The results remained insignificant when the analyses were performed including only studies with high quality 0.25 (95% CI: -0.46 to 0.96, I<sup>2</sup> = 92%, <i>p</i> < 0.01) I<sup>2</sup> = 95%, <i>p</i> = 0.815), when TNF-α was nasal 0.60 (95% CI: -0.49 to 1.69), I<sup>2</sup> = 94%, <i>p</i> < 0.01), or serum -0.08 (95% CI: -0.48 to 0.31), I<sup>2</sup> = 29%, <i>p</i> = 0.24). In the analysis of studies measuring IFN-γ, there was also no significance of -0.67 (95% CI: -1.56 to 0.22, I<sup>2</sup> = 76%, <i>p</i> = 0.04). In conclusion, this meta-analysis suggests that the most severe patients do not have different mean TNF-α and IFN-γ values than patients with mild disease, but the heterogeneity of the studies was high. 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引用次数: 3
摘要
由呼吸道合胞病毒引起的急性细支气管炎引发炎症反应,产生和释放几种促炎细胞因子。有证据表明,它们的水平与感染的严重程度有关。本系统综述和荟萃分析旨在评估TNF-α和IFN-γ水平是否与急性病毒性细支气管炎的严重程度相关。我们检索了MEDLINE图书馆(通过PUBMED)、EMBASE、Cochrane中央对照试验登记处(Central)、科学电子在线图书馆(SciELO)、拉丁美洲加勒比健康科学文献(LILACS)、护理和相关健康文献累积索引(CINAHL)、科学网络和截至2020年4月的灰色文献。一般和亚组分析采用随机效应模型。总共包括6项研究,共有744名参与者。重度组与对照组的平均TNF-α水平无差异(95% CI: -0.53 ~ 0.82, I2 = 91%, p 2 = 92%, p 2 = 95%, p = 0.815),当TNF-α为鼻部0.60时(95% CI: -0.49 ~ 1.69), I2 = 94%, p 2 = 29%, p = 0.24)。在测量IFN-γ的研究分析中,也没有-0.67的显著性(95% CI: -1.56 ~ 0.22, I2 = 76%, p = 0.04)。综上所述,本荟萃分析提示,重症患者的TNF-α和IFN-γ均值与轻症患者并无差异,但研究的异质性较高。本文的补充数据可在https://doi.org/10.1080/08830185.2021.1889534上在线获得。
Association between TNF-α and IFN-γ levels and severity of acute viral bronchiolitis.
Acute bronchiolitis caused by the respiratory syncytial virus triggers an inflammatory response with the production and release of several pro-inflammatory cytokines. Evidence suggests that their levels are associated with the severity of the infection. This systematic review and meta-analysis aim to assess whether the levels of TNF-α and IFN-γ are associated with the severity of acute viral bronchiolitis. We searched MEDLINE libraries (via PUBMED), EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL), Scientific Electronic Library Online (SciELO), Latin American Caribbean Health Sciences Literature (LILACS), Cumulative Index to Nursing and Allied Health Literature (CINAHL), Web of Science, and the gray literature through April 2020. Random effect models were used for general and subgroup analysis. In total, six studies were included with a total of 744 participants. The mean TNF-α levels between the severe group did not differ from the control group 0.14 (95% CI: -0.53 to 0.82, I2 = 91%, p < 0.01); the heterogeneity was high. The results remained insignificant when the analyses were performed including only studies with high quality 0.25 (95% CI: -0.46 to 0.96, I2 = 92%, p < 0.01) I2 = 95%, p = 0.815), when TNF-α was nasal 0.60 (95% CI: -0.49 to 1.69), I2 = 94%, p < 0.01), or serum -0.08 (95% CI: -0.48 to 0.31), I2 = 29%, p = 0.24). In the analysis of studies measuring IFN-γ, there was also no significance of -0.67 (95% CI: -1.56 to 0.22, I2 = 76%, p = 0.04). In conclusion, this meta-analysis suggests that the most severe patients do not have different mean TNF-α and IFN-γ values than patients with mild disease, but the heterogeneity of the studies was high. Supplemental data for this article is available online at https://doi.org/10.1080/08830185.2021.1889534.
期刊介绍:
This review journal provides the most current information on basic and translational research in immunology and related fields. In addition to invited reviews, the journal accepts for publication articles and editorials on relevant topics proposed by contributors. Each issue of International Reviews of Immunology contains both solicited and unsolicited review articles, editorials, and ''In-this-Issue'' highlights. The journal also hosts reviews that position the authors'' original work relative to advances in a given field, bridging the gap between annual reviews and the original research articles.
This review series is relevant to all immunologists, molecular biologists, microbiologists, translational scientists, industry researchers, and physicians who work in basic and clinical immunology, inflammatory and allergic diseases, vaccines, and additional topics relevant to medical research and drug development that connect immunology to disciplines such as oncology, cardiovascular disease, and metabolic disorders.
Covered in International Reviews of Immunology: Basic and developmental immunology (innate and adaptive immunity; inflammation; and tumor and microbial immunology); Clinical research (mechanisms of disease in man pertaining to infectious diseases, autoimmunity, allergy, oncology / immunology); and Translational research (relevant to biomarkers, diagnostics, vaccines, and drug development).