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Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection

Although aplastic anemia (AA) does not come under the category of blood malignant diseases, the infection that frequently occurs in this bone marrow failure can make it worse. Pulmonary infection is the most prevalent but limiting clinical diagnosis. To find biomarkers predicting bacterial or bacter...

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Autores principales: Zhang, Jinping, Yang, Zefeng, Hu, Peng, Guan, Xin, Zhang, Chaoran, Zou, Yunlian, Li, Huiyuan, Yang, Tonghua, Cao, Yue, Zhao, Renbin, Li, Zengzheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626605/
https://www.ncbi.nlm.nih.gov/pubmed/36319826
http://dx.doi.org/10.1038/s41598-022-22503-7
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author Zhang, Jinping
Yang, Zefeng
Hu, Peng
Guan, Xin
Zhang, Chaoran
Zou, Yunlian
Li, Huiyuan
Yang, Tonghua
Cao, Yue
Zhao, Renbin
Li, Zengzheng
author_facet Zhang, Jinping
Yang, Zefeng
Hu, Peng
Guan, Xin
Zhang, Chaoran
Zou, Yunlian
Li, Huiyuan
Yang, Tonghua
Cao, Yue
Zhao, Renbin
Li, Zengzheng
author_sort Zhang, Jinping
collection PubMed
description Although aplastic anemia (AA) does not come under the category of blood malignant diseases, the infection that frequently occurs in this bone marrow failure can make it worse. Pulmonary infection is the most prevalent but limiting clinical diagnosis. To find biomarkers predicting bacterial or bacterial-combined fungal infections in the lungs, we reviewed 287 AA medical records including 151 without any infection, 87 with pure pulmonary bacterial infection, and 49 with bacterial and fungal infection were reviewed. There were substantial changes in IL-17F, IL-17A, IFN-γ, IL-6, IL-8, and IL-10 levels between the non-infected and lung bacterial infection groups (P < 0.05). Further, a significant variation in IL-17A, TNF-β, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-22, and IL-12p70, between the uninfected group and the pulmonary bacterial and fungal infection group (P < 0.05) was observed. The results further revealed significant differences in TNF-β, IL-12p70, IL-6, IL-8, and IL-10 between the pulmonary bacterial infection group and the fungal infection group (P < 0.05). Moreover, by calculating ROC and cut-off values, we determined that IL-6 (AUC = 0.98, Cut-off = 14.28 pg/ml, P = 0.0000) had a significant advantage than other cytokines, body temperature (AUC = 0.61, P = 0.0050), PCT (AUC = 0.57, P = 0.0592), and CRP (AUC = 0.60, P = 0.0147) in the detection of lungs bacterial infections. In addition, IL-6 (AUC = 1.00, Cut-off = 51.50 pg/ml, P = 0.000) and IL-8 (AUC = 0.87, Cut-off = 60.53 pg/ml, P = 0.0000) showed stronger advantages than other cytokines, body temperature (AUC = 0.60, P = 0.0324), PCT (AUC = 0.72, Cut-off = 0.63 ng/ml, P = 0.0000) and CRP (AUC = 0.79, Cut-off = 5.79 mg/l, P = 0.0000) in distinguishing bacteria from fungi. This may suggest that IL-8 may play a role in differentiating co-infected bacteria and fungi. Such advantages are repeated in severe aplastic anemia (SAA) and very severe aplastic anemia (VSAA).In conclusion, aberrant IL-6 elevations in AA patients may predict the likelihood of bacterial lung infection. The concurrent increase of IL-6 and IL-8, on the other hand, should signal bacterial and fungal infections in patients.These findings may help to suggest bacterial or fungal co-infection in patients with AA (Focus on VSAA and SAA).
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spelling pubmed-96266052022-11-03 Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection Zhang, Jinping Yang, Zefeng Hu, Peng Guan, Xin Zhang, Chaoran Zou, Yunlian Li, Huiyuan Yang, Tonghua Cao, Yue Zhao, Renbin Li, Zengzheng Sci Rep Article Although aplastic anemia (AA) does not come under the category of blood malignant diseases, the infection that frequently occurs in this bone marrow failure can make it worse. Pulmonary infection is the most prevalent but limiting clinical diagnosis. To find biomarkers predicting bacterial or bacterial-combined fungal infections in the lungs, we reviewed 287 AA medical records including 151 without any infection, 87 with pure pulmonary bacterial infection, and 49 with bacterial and fungal infection were reviewed. There were substantial changes in IL-17F, IL-17A, IFN-γ, IL-6, IL-8, and IL-10 levels between the non-infected and lung bacterial infection groups (P < 0.05). Further, a significant variation in IL-17A, TNF-β, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-22, and IL-12p70, between the uninfected group and the pulmonary bacterial and fungal infection group (P < 0.05) was observed. The results further revealed significant differences in TNF-β, IL-12p70, IL-6, IL-8, and IL-10 between the pulmonary bacterial infection group and the fungal infection group (P < 0.05). Moreover, by calculating ROC and cut-off values, we determined that IL-6 (AUC = 0.98, Cut-off = 14.28 pg/ml, P = 0.0000) had a significant advantage than other cytokines, body temperature (AUC = 0.61, P = 0.0050), PCT (AUC = 0.57, P = 0.0592), and CRP (AUC = 0.60, P = 0.0147) in the detection of lungs bacterial infections. In addition, IL-6 (AUC = 1.00, Cut-off = 51.50 pg/ml, P = 0.000) and IL-8 (AUC = 0.87, Cut-off = 60.53 pg/ml, P = 0.0000) showed stronger advantages than other cytokines, body temperature (AUC = 0.60, P = 0.0324), PCT (AUC = 0.72, Cut-off = 0.63 ng/ml, P = 0.0000) and CRP (AUC = 0.79, Cut-off = 5.79 mg/l, P = 0.0000) in distinguishing bacteria from fungi. This may suggest that IL-8 may play a role in differentiating co-infected bacteria and fungi. Such advantages are repeated in severe aplastic anemia (SAA) and very severe aplastic anemia (VSAA).In conclusion, aberrant IL-6 elevations in AA patients may predict the likelihood of bacterial lung infection. The concurrent increase of IL-6 and IL-8, on the other hand, should signal bacterial and fungal infections in patients.These findings may help to suggest bacterial or fungal co-infection in patients with AA (Focus on VSAA and SAA). Nature Publishing Group UK 2022-11-01 /pmc/articles/PMC9626605/ /pubmed/36319826 http://dx.doi.org/10.1038/s41598-022-22503-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Jinping
Yang, Zefeng
Hu, Peng
Guan, Xin
Zhang, Chaoran
Zou, Yunlian
Li, Huiyuan
Yang, Tonghua
Cao, Yue
Zhao, Renbin
Li, Zengzheng
Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
title Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
title_full Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
title_fullStr Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
title_full_unstemmed Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
title_short Cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
title_sort cytokines help suggest aplastic anemia with pulmonary bacterial or co-fungal infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626605/
https://www.ncbi.nlm.nih.gov/pubmed/36319826
http://dx.doi.org/10.1038/s41598-022-22503-7
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