Single-cell transcriptome analysis reveals the regulatory effects of artesunate on splenic immune cells in polymicrobial sepsis
Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune c...
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Abstract | Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune cells remain limited. This study aimed to investigate the protective effects and underlying mechanism of artesunate (ART) on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing (scRNA-seq) and experimental validations. The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis. ART could restore neutrophils’ chemotaxis and immune function in the septic spleen. It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis. ART also promoted the differentiation and activity of splenic B cells in mice with sepsis. These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host. Overall, this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis, thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis.
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•Identifying the therapeutic effect of ART on splenic immune cells in sepsis mice.•Providing a comprehensive single-cell atlas of septic spleen under ART treatment.•ART inhibits M1-like macrophage recruitment and Treg activation in sepsis mice.•ART alleviates dysfunctions of splenic B, NK, and neutrophil cells during sepsis. |
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AbstractList | Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune cells remain limited. This study aimed to investigate the protective effects and underlying mechanism of artesunate (ART) on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing (scRNA-seq) and experimental validations. The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis. ART could restore neutrophils’ chemotaxis and immune function in the septic spleen. It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis. ART also promoted the differentiation and activity of splenic B cells in mice with sepsis. These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host. Overall, this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis, thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis.
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Identifying the therapeutic effect of ART on splenic immune cells in sepsis mice.
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Providing a comprehensive single-cell atlas of septic spleen under ART treatment.
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ART inhibits M1-like macrophage recruitment and Treg activation in sepsis mice.
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ART alleviates dysfunctions of splenic B, NK, and neutrophil cells during sepsis. Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune cells remain limited. This study aimed to investigate the protective effects and underlying mechanism of artesunate (ART) on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing (scRNA-seq) and experimental validations. The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis. ART could restore neutrophils’ chemotaxis and immune function in the septic spleen. It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis. ART also promoted the differentiation and activity of splenic B cells in mice with sepsis. These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host. Overall, this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis, thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis. [Display omitted] •Identifying the therapeutic effect of ART on splenic immune cells in sepsis mice.•Providing a comprehensive single-cell atlas of septic spleen under ART treatment.•ART inhibits M1-like macrophage recruitment and Treg activation in sepsis mice.•ART alleviates dysfunctions of splenic B, NK, and neutrophil cells during sepsis. Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction.Studies on the therapeutic effect and mechanism of immunomod-ulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various im-mune cells remain limited.This study aimed to investigate the protective effects and underlying mechanism of artesunate(ART)on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing(scRNA-seq)and experimental validations.The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis.ART could restore neutrophils'chemotaxis and immune function in the septic spleen.It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis.ART also promoted the differentiation and activity of splenic B cells in mice with sepsis.These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host.Overall,this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis,thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis. Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune cells remain limited. This study aimed to investigate the protective effects and underlying mechanism of artesunate (ART) on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing (scRNA-seq) and experimental validations. The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis. ART could restore neutrophils' chemotaxis and immune function in the septic spleen. It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis. ART also promoted the differentiation and activity of splenic B cells in mice with sepsis. These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host. Overall, this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis, thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis. Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune cells remain limited. This study aimed to investigate the protective effects and underlying mechanism of artesunate (ART) on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing (scRNA-seq) and experimental validations. The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis. ART could restore neutrophils' chemotaxis and immune function in the septic spleen. It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis. ART also promoted the differentiation and activity of splenic B cells in mice with sepsis. These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host. Overall, this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis, thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis.Sepsis is characterized by a severe and life-threatening host immune response to polymicrobial infection accompanied by organ dysfunction. Studies on the therapeutic effect and mechanism of immunomodulatory drugs on the sepsis-induced hyperinflammatory or immunosuppression states of various immune cells remain limited. This study aimed to investigate the protective effects and underlying mechanism of artesunate (ART) on the splenic microenvironment of cecal ligation and puncture-induced sepsis model mice using single-cell RNA sequencing (scRNA-seq) and experimental validations. The scRNA-seq analysis revealed that ART inhibited the activation of pro-inflammatory macrophages recruited during sepsis. ART could restore neutrophils' chemotaxis and immune function in the septic spleen. It inhibited the activation of T regulatory cells but promoted the cytotoxic function of natural killer cells during sepsis. ART also promoted the differentiation and activity of splenic B cells in mice with sepsis. These results indicated that ART could alleviate the inflammatory and/or immunosuppressive states of various immune cells involved in sepsis to balance the immune homeostasis within the host. Overall, this study provided a comprehensive investigation of the regulatory effect of ART on the splenic microenvironment in sepsis, thus contributing to the application of ART as adjunctive therapy for the clinical treatment of sepsis. |
Author | Guo, Qiuyan Liu, Jing Wong, Yin Kwan Zhang, Qian Gao, Peng Bai, Yunmeng He, Xueling Chen, Jiayun Luo, Piao Gu, Liwei Xie, Lulin Cheng, Guangqing Wang, Chen Wang, Jigang |
AuthorAffiliation | State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing,100700,China;Department of Nephrology,Shenzhen Key Laboratory of Kidney Diseases,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,The First Affiliated Hospital,Southern University of Science and Technology,Shenzhen,Guangdong,518020,China%State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing,100700,China%Department of Nephrology,Shenzhen Key Laboratory of Kidney Diseases,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,The First Affiliated Hospital,Southern University of Science and Technology,Shenzhen,Guangdong,518020,China%Department of Gastroenterology,Shenzhen Hospital,Southern Medical Un |
AuthorAffiliation_xml | – name: State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing,100700,China;Department of Nephrology,Shenzhen Key Laboratory of Kidney Diseases,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,The First Affiliated Hospital,Southern University of Science and Technology,Shenzhen,Guangdong,518020,China%State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing,100700,China%Department of Nephrology,Shenzhen Key Laboratory of Kidney Diseases,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,The First Affiliated Hospital,Southern University of Science and Technology,Shenzhen,Guangdong,518020,China%Department of Gastroenterology,Shenzhen Hospital,Southern Medical University,Shenzhen,Guangdong,518020,China |
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Cites_doi | 10.1093/bioinformatics/bty560 10.1126/sciimmunol.aau6085 10.1016/j.immuni.2021.10.012 10.3389/fimmu.2021.696536 10.1038/s41467-021-21246-9 10.1002/cpim.110 10.1038/s41401-021-00634-3 10.1016/j.chembiol.2022.06.011 10.3389/fimmu.2022.861670 10.1067/msy.2000.107282 10.1038/nbt.2859 10.1007/s11926-018-0764-y 10.1007/s11427-019-9550-4 10.21037/atm.2020.02.35 10.1093/intimm/dxv028 10.1038/nri.2017.36 10.1186/s13054-021-03481-0 10.1186/s13054-016-1250-4 10.1001/jama.2016.0287 10.1016/j.actbio.2019.02.006 10.1007/s10753-015-0290-2 10.1152/ajplung.00477.2005 10.1189/jlb.0607371 10.1016/j.ygeno.2021.01.026 10.1002/pros.23301 10.1016/j.cell.2019.05.031 10.1378/chest.118.2.503 10.1038/nri3552 10.1038/s41401-022-00978-4 10.1016/j.gene.2020.144969 10.1172/JCI128075 10.1016/j.pharmthera.2016.07.002 10.1172/JCI82224 10.1081/IPH-100103856 10.4049/jimmunol.1701618 10.1172/JCI27227 10.1016/j.mam.2017.07.003 10.7150/thno.72760 10.3390/cancers11071037 |
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Keywords | Sepsis Immunomodulatory activity Single-cell RNA sequencing Artesunate |
Language | English |
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Publisher | Elsevier B.V Department of Nephrology,Shenzhen Key Laboratory of Kidney Diseases,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,The First Affiliated Hospital,Southern University of Science and Technology,Shenzhen,Guangdong,518020,China%State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing,100700,China%Department of Nephrology,Shenzhen Key Laboratory of Kidney Diseases,and Shenzhen Clinical Research Centre for Geriatrics,Shenzhen People's Hospital,The First Affiliated Hospital,Southern University of Science and Technology,Shenzhen,Guangdong,518020,China%Department of Gastroenterology,Shenzhen Hospital,Southern Medical University,Shenzhen,Guangdong,518020,China State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Artemisinin Research Center,and Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing,100700,China Xi'an Jiaotong University Elsevier |
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References | van der Poll, van de Veerdonk, Scicluna (bib4) 2017; 17 Gregory, Raju, Winandy (bib24) 2006; 116 Tong, Chen, He (bib9) 2022; 43 Song, Chung, Chaudry (bib23) 2000; 128 Zhang, Luo, Xia (bib40) 2022; 29 Leliefeld, Wessels, Leenen (bib34) 2016; 20 Venet, Chung, Monneret (bib36) 2008; 83 Stuart, Butler, Hoffman (bib20) 2019; 177 Zhang, Zhang, Jiang (bib10) 2020; 63 Hedlund, Deng (bib14) 2018; 59 Wen, Cai, Ye (bib15) 2020; 8 Trapnell, Cacchiarelli, Grimsby (bib21) 2014; 32 Dinarello (bib28) 2000; 118 Jensen, Sjaastad, Griffith (bib26) 2018; 200 Lewis, Williams, Eisenbarth (bib5) 2019; 4 Yao, Li, Wang (bib17) 2022; 12 Darden, Dong, Brusko (bib30) 2021; 12 Mu, Wang (bib7) 2018; 20 Qi, Yu, Sun (bib25) 2021; 25 Hotchkiss, Monneret, Payen (bib3) 2013; 13 Kim, Ner-Gaon, Varon (bib37) 2020; 130 Chen, Zhou, Chen (bib19) 2018; 34 Wang, Zhang, Liu (bib16) 2021; 113 Delano, Ward (bib29) 2016; 126 Yang, Deng, Zhao (bib32) 2019; 88 Luo, Zhang, Zhong (bib39) 2022; 9 Chousterman, Swirski (bib38) 2015; 27 Singer, Deutschman, Seymour (bib1) 2016; 315 Wang, Zhuo, Luo (bib31) 2017; 77 Zhang, Wang, Chen (bib12) 2020; 759 Cao, Jin, Fei (bib11) 2016; 39 Sjaastad, Jensen, Berton (bib18) 2020; 131 Gray, Biron-Girard, Wakeley (bib35) 2022; 13 Liu, Malik (bib33) 2006; 290 Altamura, Caradonna, Amati (bib6) 2001; 23 van der Poll, Shankar-Hari, Wiersinga (bib2) 2021; 54 Lin, Wei, Hu (bib13) 2021; 42 Jin, Guerrero-Juarez, Zhang (bib22) 2021; 12 Atsaves, Leventaki, Rassidakis (bib27) 2019; 11 Hou, Huang (bib8) 2016; 166 Zhang (10.1016/j.jpha.2023.02.006_bib10) 2020; 63 Zhang (10.1016/j.jpha.2023.02.006_bib12) 2020; 759 Wang (10.1016/j.jpha.2023.02.006_bib31) 2017; 77 Cao (10.1016/j.jpha.2023.02.006_bib11) 2016; 39 Darden (10.1016/j.jpha.2023.02.006_bib30) 2021; 12 Leliefeld (10.1016/j.jpha.2023.02.006_bib34) 2016; 20 Trapnell (10.1016/j.jpha.2023.02.006_bib21) 2014; 32 Venet (10.1016/j.jpha.2023.02.006_bib36) 2008; 83 Zhang (10.1016/j.jpha.2023.02.006_bib40) 2022; 29 Liu (10.1016/j.jpha.2023.02.006_bib33) 2006; 290 Wen (10.1016/j.jpha.2023.02.006_bib15) 2020; 8 Jin (10.1016/j.jpha.2023.02.006_bib22) 2021; 12 Yang (10.1016/j.jpha.2023.02.006_bib32) 2019; 88 Hotchkiss (10.1016/j.jpha.2023.02.006_bib3) 2013; 13 Stuart (10.1016/j.jpha.2023.02.006_bib20) 2019; 177 Lin (10.1016/j.jpha.2023.02.006_bib13) 2021; 42 Sjaastad (10.1016/j.jpha.2023.02.006_bib18) 2020; 131 Wang (10.1016/j.jpha.2023.02.006_bib16) 2021; 113 Qi (10.1016/j.jpha.2023.02.006_bib25) 2021; 25 Hou (10.1016/j.jpha.2023.02.006_bib8) 2016; 166 Dinarello (10.1016/j.jpha.2023.02.006_bib28) 2000; 118 Mu (10.1016/j.jpha.2023.02.006_bib7) 2018; 20 Song (10.1016/j.jpha.2023.02.006_bib23) 2000; 128 Hedlund (10.1016/j.jpha.2023.02.006_bib14) 2018; 59 van der Poll (10.1016/j.jpha.2023.02.006_bib4) 2017; 17 Atsaves (10.1016/j.jpha.2023.02.006_bib27) 2019; 11 Chousterman (10.1016/j.jpha.2023.02.006_bib38) 2015; 27 Luo (10.1016/j.jpha.2023.02.006_bib39) 2022; 9 Altamura (10.1016/j.jpha.2023.02.006_bib6) 2001; 23 van der Poll (10.1016/j.jpha.2023.02.006_bib2) 2021; 54 Delano (10.1016/j.jpha.2023.02.006_bib29) 2016; 126 Kim (10.1016/j.jpha.2023.02.006_bib37) 2020; 130 Yao (10.1016/j.jpha.2023.02.006_bib17) 2022; 12 Tong (10.1016/j.jpha.2023.02.006_bib9) 2022; 43 Gregory (10.1016/j.jpha.2023.02.006_bib24) 2006; 116 Lewis (10.1016/j.jpha.2023.02.006_bib5) 2019; 4 Jensen (10.1016/j.jpha.2023.02.006_bib26) 2018; 200 Gray (10.1016/j.jpha.2023.02.006_bib35) 2022; 13 Chen (10.1016/j.jpha.2023.02.006_bib19) 2018; 34 Singer (10.1016/j.jpha.2023.02.006_bib1) 2016; 315 |
References_xml | – volume: 29 start-page: 1248 year: 2022 end-page: 1259.e6 ident: bib40 article-title: Capsaicin ameliorates inflammation in a TRPV1-independent mechanism by inhibiting PKM2-LDHA-mediated Warburg effect in sepsis publication-title: Cell Chem. Biol. – volume: 4 year: 2019 ident: bib5 article-title: Structure and function of the immune system in the spleen publication-title: Sci. Immunol. – volume: 12 year: 2021 ident: bib22 article-title: Inference and analysis of cell-cell communication using CellChat publication-title: Nat. Commun. – volume: 32 start-page: 381 year: 2014 end-page: 386 ident: bib21 article-title: The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells publication-title: Nat. Biotechnol. – volume: 126 start-page: 23 year: 2016 end-page: 31 ident: bib29 article-title: Sepsis-induced immune dysfunction: Can immune therapies reduce mortality? publication-title: J. Clin. Invest. – volume: 128 start-page: 133 year: 2000 end-page: 138 ident: bib23 article-title: IL-4-induced activation of the Stat6 pathway contributes to the suppression of cell-mediated immunity and death in sepsis publication-title: Surgery – volume: 315 start-page: 801 year: 2016 end-page: 810 ident: bib1 article-title: The third international consensus definitions for sepsis and septic shock (sepsis-3) publication-title: JAMA – volume: 290 start-page: L622 year: 2006 end-page: L645 ident: bib33 article-title: NF-κB activation as a pathological mechanism of septic shock and inflammation publication-title: Am. J. Physiol. Lung Cell. Mol. Physiol. – volume: 12 start-page: 4606 year: 2022 end-page: 4628 ident: bib17 article-title: Single-cell transcriptome profiling of the immune space-time landscape reveals dendritic cell regulatory program in polymicrobial sepsis publication-title: Theranostics – volume: 131 year: 2020 ident: bib18 article-title: Inducing experimental polymicrobial sepsis by cecal ligation and puncture publication-title: Curr. Protoc. Immunol. – volume: 43 start-page: 3055 year: 2022 end-page: 3061 ident: bib9 article-title: Artemisinin derivative SM934 in the treatment of autoimmune and inflammatory diseases: Therapeutic effects and molecular mechanisms publication-title: Acta. Pharmacol. Sin. – volume: 113 start-page: 1219 year: 2021 end-page: 1233 ident: bib16 article-title: Single-cell RNA sequencing reveals the sustained immune cell dysfunction in the pathogenesis of sepsis secondary to bacterial pneumonia publication-title: Genomics – volume: 27 start-page: 537 year: 2015 end-page: 541 ident: bib38 article-title: Innate response activator B cells: Origins and functions publication-title: Int. Immunol. – volume: 83 start-page: 523 year: 2008 end-page: 535 ident: bib36 article-title: Regulatory T cell populations in sepsis and trauma publication-title: J. Leukoc. Biol. – volume: 23 start-page: 153 year: 2001 end-page: 161 ident: bib6 article-title: Splenectomy and sepsis: the role of the spleen in the immune-mediated bacterial clearance publication-title: Immunopharmacol. Immunotoxicol. – volume: 11 year: 2019 ident: bib27 article-title: AP-1 transcription factors as regulators of immune responses in cancer publication-title: Cancers (Basel) – volume: 759 year: 2020 ident: bib12 article-title: Artesunate ameliorates sepsis-induced acute lung injury by activating the mTOR/AKT/PI3K axis publication-title: Gene – volume: 12 year: 2021 ident: bib30 article-title: A novel single cell RNA-seq analysis of non-myeloid circulating cells in late sepsis publication-title: Front. Immunol. – volume: 77 start-page: 708 year: 2017 end-page: 717 ident: bib31 article-title: Androgen deprivation accelerates the prostatic urethra wound healing after thulium laser resection of the prostate by promoting re-epithelialization and regulating the macrophage polarization publication-title: Prostate – volume: 130 start-page: 3238 year: 2020 end-page: 3252 ident: bib37 article-title: Post-sepsis immunosuppression depends on NKT cell regulation of mTOR/IFN-γ in NK cells publication-title: J. Clin. Invest. – volume: 88 start-page: 392 year: 2019 end-page: 405 ident: bib32 article-title: Porous Se@SiO publication-title: Acta Biomater. – volume: 63 start-page: 737 year: 2020 end-page: 749 ident: bib10 article-title: Dihydroartemisinin regulates the immune system by promotion of CD8 publication-title: Sci. China Life Sci. – volume: 25 year: 2021 ident: bib25 article-title: Identification and characterization of neutrophil heterogeneity in sepsis publication-title: Crit. Care – volume: 118 start-page: 503 year: 2000 end-page: 508 ident: bib28 article-title: Proinflammatory cytokines publication-title: Chest – volume: 13 start-page: 862 year: 2013 end-page: 874 ident: bib3 article-title: Sepsis-induced immunosuppression: From cellular dysfunctions to immunotherapy publication-title: Nat. Rev. Immunol. – volume: 116 start-page: 1327 year: 2006 end-page: 1336 ident: bib24 article-title: Mast cell IL-4 expression is regulated by Ikaros and influences encephalitogenic Th1 responses in EAE publication-title: J. Clin. Invest. – volume: 54 start-page: 2450 year: 2021 end-page: 2464 ident: bib2 article-title: The immunology of sepsis publication-title: Immunity – volume: 166 start-page: 123 year: 2016 end-page: 127 ident: bib8 article-title: Immune suppressive properties of artemisinin family drugs publication-title: Pharmacol. Ther. – volume: 200 start-page: 1543 year: 2018 end-page: 1553 ident: bib26 article-title: Sepsis-Induced T Cell Immunoparalysis: The ins and outs of impaired T cell immunity publication-title: J. Immunol. – volume: 20 year: 2016 ident: bib34 article-title: The role of neutrophils in immune dysfunction during severe inflammation publication-title: Crit. Care – volume: 17 start-page: 407 year: 2017 end-page: 420 ident: bib4 article-title: The immunopathology of sepsis and potential therapeutic targets publication-title: Nat. Rev. Immunol. – volume: 39 start-page: 651 year: 2016 end-page: 662 ident: bib11 article-title: Artesunate protects against sepsis-induced lung injury via heme oxygenase-1 modulation publication-title: Inflammation – volume: 20 year: 2018 ident: bib7 article-title: Artemisinins-a promising new treatment for systemic lupus erythematosus: A descriptive review publication-title: Curr. Rheumatol. Rep. – volume: 177 start-page: 1888 year: 2019 end-page: 1902.e21 ident: bib20 article-title: Comprehensive integration of single-cell data publication-title: Cell – volume: 42 start-page: 1069 year: 2021 end-page: 1079 ident: bib13 article-title: Artemisinin improves neurocognitive deficits associated with sepsis by activating the AMPK axis in microglia publication-title: Acta Pharmacol. Sin. – volume: 9 year: 2022 ident: bib39 article-title: Celastrol mitigates inflammation in sepsis by inhibiting the PKM2-dependent Warburg effect publication-title: Mil. Med. Res. – volume: 59 start-page: 36 year: 2018 end-page: 46 ident: bib14 article-title: Single-cell RNA sequencing: Technical advancements and biological applications publication-title: Mol. Aspects Med. – volume: 34 start-page: i884 year: 2018 end-page: i890 ident: bib19 article-title: fastp: An ultra-fast all-in-one FASTQ preprocessor publication-title: Bioinformatics – volume: 13 year: 2022 ident: bib35 article-title: Negative immune checkpoint protein, VISTA, regulates the CD4 publication-title: Front. Immunol. – volume: 8 year: 2020 ident: bib15 article-title: Single-cell transcriptomics reveals the alteration of peripheral blood mononuclear cells driven by sepsis publication-title: Ann. Transl. Med. – volume: 34 start-page: i884 year: 2018 ident: 10.1016/j.jpha.2023.02.006_bib19 article-title: fastp: An ultra-fast all-in-one FASTQ preprocessor publication-title: Bioinformatics doi: 10.1093/bioinformatics/bty560 – volume: 4 year: 2019 ident: 10.1016/j.jpha.2023.02.006_bib5 article-title: Structure and function of the immune system in the spleen publication-title: Sci. Immunol. doi: 10.1126/sciimmunol.aau6085 – volume: 54 start-page: 2450 year: 2021 ident: 10.1016/j.jpha.2023.02.006_bib2 article-title: The immunology of sepsis publication-title: Immunity doi: 10.1016/j.immuni.2021.10.012 – volume: 12 year: 2021 ident: 10.1016/j.jpha.2023.02.006_bib30 article-title: A novel single cell RNA-seq analysis of non-myeloid circulating cells in late sepsis publication-title: Front. Immunol. doi: 10.3389/fimmu.2021.696536 – volume: 12 year: 2021 ident: 10.1016/j.jpha.2023.02.006_bib22 article-title: Inference and analysis of cell-cell communication using CellChat publication-title: Nat. Commun. doi: 10.1038/s41467-021-21246-9 – volume: 131 year: 2020 ident: 10.1016/j.jpha.2023.02.006_bib18 article-title: Inducing experimental polymicrobial sepsis by cecal ligation and puncture publication-title: Curr. Protoc. Immunol. doi: 10.1002/cpim.110 – volume: 42 start-page: 1069 year: 2021 ident: 10.1016/j.jpha.2023.02.006_bib13 article-title: Artemisinin improves neurocognitive deficits associated with sepsis by activating the AMPK axis in microglia publication-title: Acta Pharmacol. Sin. doi: 10.1038/s41401-021-00634-3 – volume: 29 start-page: 1248 year: 2022 ident: 10.1016/j.jpha.2023.02.006_bib40 article-title: Capsaicin ameliorates inflammation in a TRPV1-independent mechanism by inhibiting PKM2-LDHA-mediated Warburg effect in sepsis publication-title: Cell Chem. Biol. doi: 10.1016/j.chembiol.2022.06.011 – volume: 13 year: 2022 ident: 10.1016/j.jpha.2023.02.006_bib35 article-title: Negative immune checkpoint protein, VISTA, regulates the CD4+ Treg population during sepsis progression to promote acute sepsis recovery and survival publication-title: Front. Immunol. doi: 10.3389/fimmu.2022.861670 – volume: 128 start-page: 133 year: 2000 ident: 10.1016/j.jpha.2023.02.006_bib23 article-title: IL-4-induced activation of the Stat6 pathway contributes to the suppression of cell-mediated immunity and death in sepsis publication-title: Surgery doi: 10.1067/msy.2000.107282 – volume: 32 start-page: 381 year: 2014 ident: 10.1016/j.jpha.2023.02.006_bib21 article-title: The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells publication-title: Nat. Biotechnol. doi: 10.1038/nbt.2859 – volume: 20 year: 2018 ident: 10.1016/j.jpha.2023.02.006_bib7 article-title: Artemisinins – a promising new treatment for systemic lupus erythematosus: A descriptive review publication-title: Curr. Rheumatol. Rep. doi: 10.1007/s11926-018-0764-y – volume: 63 start-page: 737 year: 2020 ident: 10.1016/j.jpha.2023.02.006_bib10 article-title: Dihydroartemisinin regulates the immune system by promotion of CD8+ T lymphocytes and suppression of B cell responses publication-title: Sci. China Life Sci. doi: 10.1007/s11427-019-9550-4 – volume: 8 year: 2020 ident: 10.1016/j.jpha.2023.02.006_bib15 article-title: Single-cell transcriptomics reveals the alteration of peripheral blood mononuclear cells driven by sepsis publication-title: Ann. Transl. Med. doi: 10.21037/atm.2020.02.35 – volume: 27 start-page: 537 year: 2015 ident: 10.1016/j.jpha.2023.02.006_bib38 article-title: Innate response activator B cells: Origins and functions publication-title: Int. Immunol. doi: 10.1093/intimm/dxv028 – volume: 17 start-page: 407 year: 2017 ident: 10.1016/j.jpha.2023.02.006_bib4 article-title: The immunopathology of sepsis and potential therapeutic targets publication-title: Nat. Rev. Immunol. doi: 10.1038/nri.2017.36 – volume: 25 year: 2021 ident: 10.1016/j.jpha.2023.02.006_bib25 article-title: Identification and characterization of neutrophil heterogeneity in sepsis publication-title: Crit. Care doi: 10.1186/s13054-021-03481-0 – volume: 20 year: 2016 ident: 10.1016/j.jpha.2023.02.006_bib34 article-title: The role of neutrophils in immune dysfunction during severe inflammation publication-title: Crit. Care doi: 10.1186/s13054-016-1250-4 – volume: 315 start-page: 801 year: 2016 ident: 10.1016/j.jpha.2023.02.006_bib1 article-title: The third international consensus definitions for sepsis and septic shock (sepsis-3) publication-title: JAMA doi: 10.1001/jama.2016.0287 – volume: 88 start-page: 392 year: 2019 ident: 10.1016/j.jpha.2023.02.006_bib32 article-title: Porous Se@SiO2 nanosphere-coated catheter accelerates prostatic urethra wound healing by modulating macrophage polarization through reactive oxygen species-NF-κB pathway inhibition publication-title: Acta Biomater. doi: 10.1016/j.actbio.2019.02.006 – volume: 39 start-page: 651 year: 2016 ident: 10.1016/j.jpha.2023.02.006_bib11 article-title: Artesunate protects against sepsis-induced lung injury via heme oxygenase-1 modulation publication-title: Inflammation doi: 10.1007/s10753-015-0290-2 – volume: 290 start-page: L622 year: 2006 ident: 10.1016/j.jpha.2023.02.006_bib33 article-title: NF-κB activation as a pathological mechanism of septic shock and inflammation publication-title: Am. J. Physiol. Lung Cell. Mol. Physiol. doi: 10.1152/ajplung.00477.2005 – volume: 83 start-page: 523 year: 2008 ident: 10.1016/j.jpha.2023.02.006_bib36 article-title: Regulatory T cell populations in sepsis and trauma publication-title: J. Leukoc. Biol. doi: 10.1189/jlb.0607371 – volume: 113 start-page: 1219 year: 2021 ident: 10.1016/j.jpha.2023.02.006_bib16 article-title: Single-cell RNA sequencing reveals the sustained immune cell dysfunction in the pathogenesis of sepsis secondary to bacterial pneumonia publication-title: Genomics doi: 10.1016/j.ygeno.2021.01.026 – volume: 77 start-page: 708 year: 2017 ident: 10.1016/j.jpha.2023.02.006_bib31 article-title: Androgen deprivation accelerates the prostatic urethra wound healing after thulium laser resection of the prostate by promoting re-epithelialization and regulating the macrophage polarization publication-title: Prostate doi: 10.1002/pros.23301 – volume: 177 start-page: 1888 year: 2019 ident: 10.1016/j.jpha.2023.02.006_bib20 article-title: Comprehensive integration of single-cell data publication-title: Cell doi: 10.1016/j.cell.2019.05.031 – volume: 118 start-page: 503 year: 2000 ident: 10.1016/j.jpha.2023.02.006_bib28 article-title: Proinflammatory cytokines publication-title: Chest doi: 10.1378/chest.118.2.503 – volume: 13 start-page: 862 year: 2013 ident: 10.1016/j.jpha.2023.02.006_bib3 article-title: Sepsis-induced immunosuppression: From cellular dysfunctions to immunotherapy publication-title: Nat. Rev. Immunol. doi: 10.1038/nri3552 – volume: 43 start-page: 3055 year: 2022 ident: 10.1016/j.jpha.2023.02.006_bib9 article-title: Artemisinin derivative SM934 in the treatment of autoimmune and inflammatory diseases: Therapeutic effects and molecular mechanisms publication-title: Acta. Pharmacol. Sin. doi: 10.1038/s41401-022-00978-4 – volume: 759 year: 2020 ident: 10.1016/j.jpha.2023.02.006_bib12 article-title: Artesunate ameliorates sepsis-induced acute lung injury by activating the mTOR/AKT/PI3K axis publication-title: Gene doi: 10.1016/j.gene.2020.144969 – volume: 130 start-page: 3238 year: 2020 ident: 10.1016/j.jpha.2023.02.006_bib37 article-title: Post-sepsis immunosuppression depends on NKT cell regulation of mTOR/IFN-γ in NK cells publication-title: J. Clin. Invest. doi: 10.1172/JCI128075 – volume: 166 start-page: 123 year: 2016 ident: 10.1016/j.jpha.2023.02.006_bib8 article-title: Immune suppressive properties of artemisinin family drugs publication-title: Pharmacol. Ther. doi: 10.1016/j.pharmthera.2016.07.002 – volume: 126 start-page: 23 year: 2016 ident: 10.1016/j.jpha.2023.02.006_bib29 article-title: Sepsis-induced immune dysfunction: Can immune therapies reduce mortality? publication-title: J. Clin. Invest. doi: 10.1172/JCI82224 – volume: 9 year: 2022 ident: 10.1016/j.jpha.2023.02.006_bib39 article-title: Celastrol mitigates inflammation in sepsis by inhibiting the PKM2-dependent Warburg effect publication-title: Mil. Med. Res. – volume: 23 start-page: 153 year: 2001 ident: 10.1016/j.jpha.2023.02.006_bib6 article-title: Splenectomy and sepsis: The role of the spleen in the immune-mediated bacterial clearance publication-title: Immunopharmacol. Immunotoxicol. doi: 10.1081/IPH-100103856 – volume: 200 start-page: 1543 year: 2018 ident: 10.1016/j.jpha.2023.02.006_bib26 article-title: Sepsis-induced T Cell immunoparalysis: The ins and outs of impaired T cell immunity publication-title: J. Immunol. doi: 10.4049/jimmunol.1701618 – volume: 116 start-page: 1327 year: 2006 ident: 10.1016/j.jpha.2023.02.006_bib24 article-title: Mast cell IL-4 expression is regulated by Ikaros and influences encephalitogenic Th1 responses in EAE publication-title: J. Clin. Invest. doi: 10.1172/JCI27227 – volume: 59 start-page: 36 year: 2018 ident: 10.1016/j.jpha.2023.02.006_bib14 article-title: Single-cell RNA sequencing: Technical advancements and biological applications publication-title: Mol. Aspects Med. doi: 10.1016/j.mam.2017.07.003 – volume: 12 start-page: 4606 year: 2022 ident: 10.1016/j.jpha.2023.02.006_bib17 article-title: Single-cell transcriptome profiling of the immune space-time landscape reveals dendritic cell regulatory program in polymicrobial sepsis publication-title: Theranostics doi: 10.7150/thno.72760 – volume: 11 year: 2019 ident: 10.1016/j.jpha.2023.02.006_bib27 article-title: AP-1 transcription factors as regulators of immune responses in cancer publication-title: Cancers (Basel) doi: 10.3390/cancers11071037 |
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