Tolerogenic probiotics Lactobacillus delbrueckii and Lactobacillus rhamnosus promote anti‐inflammatory profile of macrophages‐derived monocytes of newly diagnosed patients with systemic lupus erythematosus
Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self‐tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalance...
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Published in | Cell biochemistry and function Vol. 42; no. 2; pp. e3981 - n/a |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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England
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01.03.2024
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ISSN | 0263-6484 1099-0844 1099-0844 |
DOI | 10.1002/cbf.3981 |
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Abstract | Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self‐tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real‐time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen – DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1‐β, IL‐12, tumor necrosis factor α [TNF‐α], IL‐10, and transforming growth factor beta [TGF‐β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient‐derived macrophage‐derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL‐10 and TGF‐β and decreased levels of IL‐12, IL1‐β, and TNF‐α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro‐inflammatory cytokines in lupus patients, there was a higher expression of anti‐inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on MDMs from both healthy and lupus subjects.
Significance statement
Macrophages have been implicated as a factor in the development of systemic lupus erythematosus through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on macrophage‐derived monocytes (MDMs) from both healthy and lupus subjects. In both control and patient‐derived MDMs, the probiotic groups showed a decrease in cluster of differentiation (CD) 14, CD80, and Human Leukocyte Antigen – DR expression compared to the lipopolysaccharides (LPS) group. Also observed the increased levels of interleukin (IL)‐10 and transforming growth factor beta and decreased levels of IL‐12, IL1‐β, and tumor necrosis factor α in MDMs from both healthy and lupus subjects compared to the LPS groups. |
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AbstractList | Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self-tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real-time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen - DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1-β, IL-12, tumor necrosis factor α [TNF-α], IL-10, and transforming growth factor beta [TGF-β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient-derived macrophage-derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL-10 and TGF-β and decreased levels of IL-12, IL1-β, and TNF-α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro-inflammatory cytokines in lupus patients, there was a higher expression of anti-inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti-inflammatory effects on MDMs from both healthy and lupus subjects.Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self-tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real-time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen - DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1-β, IL-12, tumor necrosis factor α [TNF-α], IL-10, and transforming growth factor beta [TGF-β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient-derived macrophage-derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL-10 and TGF-β and decreased levels of IL-12, IL1-β, and TNF-α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro-inflammatory cytokines in lupus patients, there was a higher expression of anti-inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti-inflammatory effects on MDMs from both healthy and lupus subjects. Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self‐tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real‐time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen – DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1‐β, IL‐12, tumor necrosis factor α [TNF‐α], IL‐10, and transforming growth factor beta [TGF‐β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient‐derived macrophage‐derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL‐10 and TGF‐β and decreased levels of IL‐12, IL1‐β, and TNF‐α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro‐inflammatory cytokines in lupus patients, there was a higher expression of anti‐inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on MDMs from both healthy and lupus subjects. Significance statement Macrophages have been implicated as a factor in the development of systemic lupus erythematosus through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on macrophage‐derived monocytes (MDMs) from both healthy and lupus subjects. In both control and patient‐derived MDMs, the probiotic groups showed a decrease in cluster of differentiation (CD) 14, CD80, and Human Leukocyte Antigen – DR expression compared to the lipopolysaccharides (LPS) group. Also observed the increased levels of interleukin (IL)‐10 and transforming growth factor beta and decreased levels of IL‐12, IL1‐β, and tumor necrosis factor α in MDMs from both healthy and lupus subjects compared to the LPS groups. Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self‐tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real‐time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen – DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1‐β, IL‐12, tumor necrosis factor α [TNF‐α], IL‐10, and transforming growth factor beta [TGF‐β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient‐derived macrophage‐derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL‐10 and TGF‐β and decreased levels of IL‐12, IL1‐β, and TNF‐α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro‐inflammatory cytokines in lupus patients, there was a higher expression of anti‐inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on MDMs from both healthy and lupus subjects. Macrophages have been implicated as a factor in the development of systemic lupus erythematosus through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on macrophage‐derived monocytes (MDMs) from both healthy and lupus subjects. In both control and patient‐derived MDMs, the probiotic groups showed a decrease in cluster of differentiation (CD) 14, CD80, and Human Leukocyte Antigen – DR expression compared to the lipopolysaccharides (LPS) group. Also observed the increased levels of interleukin (IL)‐10 and transforming growth factor beta and decreased levels of IL‐12, IL1‐β, and tumor necrosis factor α in MDMs from both healthy and lupus subjects compared to the LPS groups. Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self-tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real-time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen - DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1-β, IL-12, tumor necrosis factor α [TNF-α], IL-10, and transforming growth factor beta [TGF-β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient-derived macrophage-derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL-10 and TGF-β and decreased levels of IL-12, IL1-β, and TNF-α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro-inflammatory cytokines in lupus patients, there was a higher expression of anti-inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti-inflammatory effects on MDMs from both healthy and lupus subjects. Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self‐tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real‐time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen – DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1‐β, IL‐12, tumor necrosis factor α [TNF‐α], IL‐10, and transforming growth factor beta [TGF‐β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient‐derived macrophage‐derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL‐10 and TGF‐β and decreased levels of IL‐12, IL1‐β, and TNF‐α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro‐inflammatory cytokines in lupus patients, there was a higher expression of anti‐inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti‐inflammatory effects on MDMs from both healthy and lupus subjects. |
Author | Mahmoudi, Mahmoud Shapouri‐Moghaddam, Abbas Tabasi, Nafiseh Sadat Javanmardi, Zahra Ahmadi, Parisa Esmaeili, Seyed‐Alireza Rafatpanah, Houshang Rezaieyazdi, Zahra Mollazadeh, Samaneh |
Author_xml | – sequence: 1 givenname: Zahra surname: Javanmardi fullname: Javanmardi, Zahra organization: Mashhad University of Medical Sciences – sequence: 2 givenname: Mahmoud surname: Mahmoudi fullname: Mahmoudi, Mahmoud organization: Mashhad University of Medical Sciences – sequence: 3 givenname: Houshang surname: Rafatpanah fullname: Rafatpanah, Houshang organization: Mashhad University of Medical Sciences – sequence: 4 givenname: Zahra surname: Rezaieyazdi fullname: Rezaieyazdi, Zahra organization: Mashhad University of Medical Sciences – sequence: 5 givenname: Abbas surname: Shapouri‐Moghaddam fullname: Shapouri‐Moghaddam, Abbas organization: Mashhad University of Medical Sciences – sequence: 6 givenname: Parisa surname: Ahmadi fullname: Ahmadi, Parisa organization: Mashhad University of Medical Sciences – sequence: 7 givenname: Samaneh surname: Mollazadeh fullname: Mollazadeh, Samaneh organization: North Khorasan University of Medical Sciences – sequence: 8 givenname: Nafiseh Sadat surname: Tabasi fullname: Tabasi, Nafiseh Sadat organization: Mashhad University of Medical Sciences – sequence: 9 givenname: Seyed‐Alireza orcidid: 0000-0002-9371-4170 surname: Esmaeili fullname: Esmaeili, Seyed‐Alireza email: Esmaeiliar@mums.ac.ir, Imunoman2009@gmail.com organization: Mashhad University of Medical Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38509733$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1093/rheumatology/kew427 10.1016/j.cell.2010.02.029 10.1186/s12882-020-01921-7 10.3389/fimmu.2017.01063 10.3389/fimmu.2017.01097 10.1046/j.1365-3083.1999.00452.x 10.1186/1475-2859-10-S1-S17 10.1186/s13075-016-0989-y 10.3109/02652048.2015.1057249 10.3389/fnut.2022.931458 10.21203/rs.3.rs-49282/v1 10.1038/s41584-021-00668-1 10.1093/cei/uxab028 10.1002/jcp.25748 10.1007/s12032-020-01435-0 10.3389/fphar.2021.759095 10.3389/fimmu.2016.00035 10.1016/j.afres.2022.100185 10.3390/microorganisms10071418 10.1007/978-3-030-55035-6_6 10.1136/annrheumdis-2018-214333 10.1101/2022.06.13.495868 10.1093/ndt/gfy195 10.1007/s13213-015-1093-2 10.1136/gut.2003.037325 10.3389/fimmu.2019.00772 10.4049/jimmunol.1501073 10.3389/fimmu.2014.00514 10.1002/jcb.26155 10.1016/j.cellsig.2013.11.004 10.1007/s12602-019-09612-y 10.1186/s12885-022-09872-y 10.1155/2023/8821610 10.1111/jam.12521 10.1111/j.1440-1746.2008.05723.x 10.1186/s12934-017-0691-z 10.1021/acsnano.3c05998 10.1155/2018/1756308 10.1371/journal.pone.0090972 10.1089/scd.2023.0047 10.3390/nu12061719 10.1371/journal.pone.0042656 10.3389/fcimb.2022.851140 10.3389/fmicb.2019.01047 10.3389/fphar.2018.00071 10.1016/j.intimp.2022.108983 10.3390/biom11060837 10.1002/ibd.21834 10.1002/jcp.27663 10.1136/gut.52.7.975 10.1371/journal.pone.0208132 10.1016/j.clim.2022.109109 10.1016/j.jff.2018.07.025 10.1371/journal.pone.0085923 10.4049/jimmunol.1002315 10.1111/sji.12162 10.1016/j.jaci.2010.12.1087 10.1016/j.humimm.2004.01.005 10.1016/j.nut.2018.02.005 10.1007/s12519-019-00229-3 10.1371/journal.pone.0008668 10.1016/j.cyto.2022.155873 10.3390/foods12040692 10.1080/20013078.2020.1793514 10.3389/fonc.2019.01512 10.1016/j.jaut.2019.01.004 10.1016/j.molimm.2017.05.027 10.1016/B0-12-370879-6/00063-6 10.1191/0961203302lu201oa 10.1016/j.jff.2014.12.040 10.3389/fimmu.2021.734008 10.1002/jcb.27203 10.3389/fimmu.2022.913007 10.1038/s41598-017-08121-8 10.1017/S0022029997002604 10.3389/fimmu.2014.00603 10.1007/s12602-021-09842-z 10.1016/j.crfs.2020.02.002 10.20517/2574-1209.2019.04 10.1002/jcp.26819 10.1007/s11926-017-0708-y |
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Keywords | macrophage probiotic systemic lupus erythematosus Lactobacillus delbrueckii M0/M1/M2 macrophages Lactobacillus rhamnosus |
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References | 2004; 65 2023; 32 2021; 24 2017; 7 2019; 2019 2017; 8 2019; 99 2019; 10 2017; 88 1999; 49 2023; 2023 2021; 207 2015; 32 2002; 11 2020; 16 2014; 26 2011; 10 2012; 18 2010; 140 2020; 12 2022; 22 2017; 232 2012; 13 2003; 52 2018; 48 2017; 118 2011; 127 2022; 244 2018; 9 2014; 5 2020; 3 2020; 9 2008; 23 2019; 234 2007; 2 2014; 9 2010; 5 2015; 13 2014; 117 2022; 154 2022; 110 2023; 12 2023; 17 2011 2023; 15 2008; 18 2019; 34 2019; 78 2020; 37 2006 2016; 18 1998; 65 2015; 195 2016; 7 2004; 53 2018; 2018 2021; 12 2021; 11 2018; 119 2021 2017; 16 2015; 20 2018; 234 2021; 17 2022; 9 2017; 56 2022; 12 2022; 13 2014; 79 2017; 19 2022; 10 2022; 2 2020; 21 2012; 7 2018; 53 2016; 8 2011; 187 2018; 13 2016; 66 e_1_2_11_70_1 e_1_2_11_72_1 Esmaeili SA (e_1_2_11_52_1) 2021; 24 e_1_2_11_32_1 e_1_2_11_55_1 e_1_2_11_78_1 e_1_2_11_30_1 e_1_2_11_57_1 e_1_2_11_36_1 e_1_2_11_51_1 e_1_2_11_74_1 e_1_2_11_13_1 e_1_2_11_34_1 e_1_2_11_53_1 e_1_2_11_76_1 e_1_2_11_11_1 Chalmers SA (e_1_2_11_16_1) 2015; 20 e_1_2_11_29_1 e_1_2_11_6_1 e_1_2_11_27_1 e_1_2_11_4_1 Khaledi A (e_1_2_11_15_1) 2016; 8 e_1_2_11_48_1 e_1_2_11_2_1 e_1_2_11_83_1 e_1_2_11_60_1 e_1_2_11_81_1 Lee J‐M (e_1_2_11_80_1) 2008; 18 e_1_2_11_20_1 e_1_2_11_45_1 e_1_2_11_66_1 e_1_2_11_47_1 e_1_2_11_68_1 e_1_2_11_89_1 e_1_2_11_24_1 e_1_2_11_41_1 e_1_2_11_62_1 e_1_2_11_87_1 e_1_2_11_8_1 e_1_2_11_22_1 e_1_2_11_43_1 e_1_2_11_64_1 e_1_2_11_17_1 e_1_2_11_59_1 e_1_2_11_38_1 e_1_2_11_19_1 e_1_2_11_50_1 e_1_2_11_71_1 e_1_2_11_90_1 e_1_2_11_10_1 e_1_2_11_31_1 e_1_2_11_56_1 e_1_2_11_77_1 e_1_2_11_58_1 e_1_2_11_79_1 e_1_2_11_14_1 e_1_2_11_35_1 e_1_2_11_73_1 e_1_2_11_12_1 e_1_2_11_33_1 e_1_2_11_54_1 e_1_2_11_75_1 e_1_2_11_7_1 e_1_2_11_28_1 e_1_2_11_5_1 Zhou H‐C (e_1_2_11_85_1) 2022; 13 e_1_2_11_26_1 e_1_2_11_3_1 e_1_2_11_49_1 e_1_2_11_82_1 e_1_2_11_21_1 e_1_2_11_44_1 e_1_2_11_67_1 e_1_2_11_46_1 e_1_2_11_69_1 e_1_2_11_88_1 e_1_2_11_25_1 e_1_2_11_40_1 Mittal G (e_1_2_11_61_1) 2007; 2 e_1_2_11_63_1 e_1_2_11_86_1 Orme J (e_1_2_11_18_1) 2012; 13 e_1_2_11_9_1 e_1_2_11_23_1 e_1_2_11_42_1 e_1_2_11_65_1 e_1_2_11_84_1 e_1_2_11_37_1 e_1_2_11_39_1 |
References_xml | – year: 2011 – volume: 7 start-page: 35 year: 2016 article-title: Clearance deficiency and cell death pathways: a model for the pathogenesis of SLE publication-title: Front Immunol – volume: 5 start-page: 603 year: 2014 article-title: TH1/TH2 paradigm extended: macrophage polarization as an unappreciated pathogen‐driven escape mechanism? publication-title: Front Immunol – volume: 7 issue: 1 year: 2017 article-title: Classification of M1/M2‐polarized human macrophages by label‐free hyperspectral reflectance confocal microscopy and multivariate analysis publication-title: Sci Rep – volume: 232 start-page: 1994 issue: 8 year: 2017 end-page: 2007 article-title: Tolerogenic probiotics: potential immunoregulators in systemic lupus erythematosus publication-title: J Cell Physiol – volume: 8 year: 2017 article-title: Gut REG3γ‐associated Lactobacillus induces anti‐inflammatory macrophages to maintain adipose tissue homeostasis publication-title: Front Immunol – volume: 37 start-page: 118 year: 2020 article-title: MicroRNAs and target molecules in bladder cancer publication-title: Med Oncol – volume: 187 start-page: 1764 issue: 4 year: 2011 end-page: 1777 article-title: Macrophage differentiation and polarization via phosphatidylinositol 3‐kinase/Akt–ERK signaling pathway conferred by serum amyloid P component publication-title: J Immunol – volume: 34 start-page: 597 issue: 4 year: 2019 end-page: 605 article-title: Mesenchymal stem cells prevent podocyte injury in lupus‐prone B6. MRL‐Faslpr mice via polarizing macrophage into an anti‐inflammatory phenotype publication-title: Nephrol Dial Transplant – volume: 119 start-page: 7865 issue: 9 year: 2018 end-page: 7872 article-title: Generation of tolerogenic dendritic cells using and as tolerogenic probiotics publication-title: J Cell Biochem – volume: 66 start-page: 171 issue: 1 year: 2016 end-page: 178 article-title: Heat‐killed yogurt‐containing lactic acid bacteria prevent cytokine‐induced barrier disruption in human intestinal Caco‐2 cells publication-title: Ann Microbiol – volume: 24 start-page: 1509 issue: 11 year: 2021 end-page: 1514 article-title: Inhibitory effects of tolerogenic probiotics on migratory potential of lupus patient‐derived DCs publication-title: Iran J Basic Med Sci – volume: 9 year: 2022 article-title: Dietary component‐induced inflammation and its amelioration by prebiotics, probiotics, and synbiotics publication-title: Front Nutr – volume: 117 start-page: 303 issue: 2 year: 2014 end-page: 319 article-title: Cross‐talk between probiotic lactobacilli and host immune system publication-title: J Appl Microbiol – volume: 9 year: 2020 article-title: Evaluating the polarization of tumor‐associated macrophages into M1 and M2 phenotypes in human cancer tissue: technicalities and challenges in routine clinical practice publication-title: Front Oncol – volume: 118 start-page: 4831 issue: 12 year: 2017 end-page: 4835 article-title: Vitamin D3 alters the expression of toll‐like receptors in peripheral blood mononuclear cells of patients with systemic lupus erythematosus publication-title: J Cell Biochem – volume: 9 issue: 3 year: 2014 article-title: Protease inhibitors from marine actinobacteria as a potential source for antimalarial compound publication-title: PLoS One – volume: 140 start-page: 871 issue: 6 year: 2010 end-page: 882 article-title: Nonresolving inflammation publication-title: Cell – volume: 26 start-page: 192 issue: 2 year: 2014 end-page: 197 article-title: Macrophage polarization and function with emphasis on the evolving roles of coordinated regulation of cellular signaling pathways publication-title: Cell Signal – volume: 12 start-page: 798 issue: 3 year: 2020 end-page: 808 article-title: Macrophage polarization induced by probiotic bacteria: a concise review publication-title: Probiotics Antimicrob Proteins – volume: 12 start-page: 692 year: 2023 article-title: The potential therapeutic role of for treatment of inflammatory bowel disease publication-title: Foods – volume: 234 start-page: 642 issue: 1 year: 2018 end-page: 649 article-title: In vivo study: Th1‐Th17 reduction in pristane‐induced systemic lupus erythematosus mice after treatment with tolerogenic probiotics publication-title: J Cell Physiol – volume: 11 start-page: 317 issue: 5 year: 2002 end-page: 321 article-title: Dysregulation of the granulocyte‐macrophage colony stimulating factor receptor is one of the causes of defective expression of CD80 antigen in systemic lupus erythematosus publication-title: Lupus – volume: 53 start-page: 1602 issue: 11 year: 2004 end-page: 1609 article-title: Modulation of human dendritic cell phenotype and function by probiotic bacteria publication-title: Gut – volume: 11 start-page: 837 issue: 6 year: 2021 article-title: Macrophage plasticity and polarization are altered in the experimental model of multiple sclerosis publication-title: Biomolecules – volume: 19 start-page: 81 issue: 12 year: 2017 article-title: Renal macrophages and dendritic cells in SLE nephritis publication-title: Curr Rheumatol Rep – volume: 78 issue: 11 year: 2019 article-title: M1/M2 polarisation state of M‐CSF blood‐derived macrophages in systemic sclerosis publication-title: Ann Rheum Dis – volume: 13 start-page: 13 year: 2022 article-title: LNA‐anti‐miR‐150 alleviates renal interstitial fibrosis by reducing pro‐inflammatory M1/M2 macrophage polarization publication-title: Front Immunol – volume: 2018 start-page: 1 year: 2018 end-page: 12 article-title: Probiotic cell‐free supernatants exhibited anti‐inflammatory and antioxidant activity on human gut epithelial cells and macrophages stimulated with LPS publication-title: Evid Based Complement Alternat Med – volume: 18 start-page: 657 issue: 4 year: 2012 end-page: 666 article-title: Anti‐inflammatory properties of dairy lactobacilli publication-title: Inflamm Bowel Dis – volume: 13 start-page: 13 year: 2022 article-title: Lactate‐driven macrophage polarization in the inflammatory microenvironment alleviates intestinal inflammation publication-title: Front Immunol – volume: 32 start-page: 465 issue: 15‐16 year: 2023 end-page: 483 article-title: Single‐cell sequencing informs that mesenchymal stem cell alleviates renal injury through regulating kidney regional immunity in lupus nephritis publication-title: Stem Cells Dev – volume: 2 start-page: 93 issue: 1 year: 2007 article-title: Immunopathogenesis of systemic lupus erythematosus publication-title: Int J Clin Rheumatol – volume: 99 start-page: 24 year: 2019 end-page: 32 article-title: PAM3 supports the generation of M2‐like macrophages from lupus patient monocytes and improves disease outcome in murine lupus publication-title: J Autoimmun – start-page: 87 year: 2021 end-page: 105 – volume: 20 start-page: 43 issue: 108 year: 2015 end-page: 49 article-title: Therapeutic targeting of macrophages in lupus nephritis publication-title: Discov Med – volume: 53 start-page: 95 year: 2018 end-page: 102 article-title: Anti‐inflammatory effect of multistrain probiotic formulation ( , , and ) publication-title: Nutrition – volume: 23 start-page: 1834 issue: 12 year: 2008 end-page: 1839 article-title: Probiotic administration alters the gut flora and attenuates colitis in mice administered dextran sodium sulfate publication-title: J Gastroenterol Hepatol – volume: 9 start-page: 71 year: 2018 article-title: Convenience versus biological significance: are PMA‐differentiated THP‐1 cells a reliable substitute for blood‐derived macrophages when studying in vitro polarization? publication-title: Front Pharmacol – start-page: 343 year: 2006 end-page: 347 – volume: 9 issue: 1 year: 2014 article-title: Local and systemic immune mechanisms underlying the anti‐colitis effects of the dairy bacterium publication-title: PLoS One – volume: 32 start-page: 669 issue: 7 year: 2015 end-page: 676 article-title: Study on the effects of microencapsulated on the mouse intestinal flora publication-title: J Microencapsul – volume: 110 year: 2022 article-title: The emerging role of microbiota‐derived short‐chain fatty acids in immunometabolism publication-title: Int Immunopharmacol – volume: 18 start-page: 1683 issue: 10 year: 2008 end-page: 1688 article-title: Antiinflammatory effect of lactic acid bacteria: inhibition of cyclooxygenase‐2 by suppressing nuclear factor‐κB in Raw264.7 macrophage cells publication-title: J Microbiol Biotechnol – volume: 9 issue: 1 year: 2020 article-title: Lactobacillus plantarum‐derived extracellular vesicles induce anti‐inflammatory M2 macrophage polarization in vitro publication-title: J Extracell Vesicles – volume: 65 start-page: 282 issue: 4 year: 2004 end-page: 290 article-title: Function and regulation of MHC class II molecules in T‐lymphocytes: of mice and men publication-title: Hum Immunol – volume: 17 start-page: 515 issue: 9 year: 2021 end-page: 532 article-title: Global epidemiology of systemic lupus erythematosus publication-title: Nat Rev Rheumatol – volume: 8 start-page: 235 issue: 3 year: 2016 end-page: 237 article-title: The role of HPaA protein as candidate vaccine against publication-title: Der Pharma Chem – volume: 5 issue: 1 year: 2010 article-title: The identification of markers of macrophage differentiation in PMA‐stimulated THP‐1 cells and monocyte‐derived macrophages publication-title: PLoS One – volume: 88 start-page: 58 year: 2017 end-page: 68 article-title: THP‐1 and human peripheral blood mononuclear cell‐derived macrophages differ in their capacity to polarize in vitro publication-title: Mol Immunol – volume: 15 start-page: 338 issue: 2 year: 2023 end-page: 350 article-title: Paraprobiotic protects intestinal damage in an experimental murine model of mucositis publication-title: Probiotics Antimicrob Proteins – volume: 2 year: 2022 article-title: Current status of probiotic and related health benefits publication-title: Appl Food Res – volume: 3 start-page: 51 year: 2020 end-page: 58 article-title: Milk fermented with R0011 induces a regulatory cytokine profile in LPS‐challenged U937 and THP‐1 macrophages publication-title: Curr Res Food Sci – volume: 13 start-page: 71 year: 2015 end-page: 79 article-title: Immunomodulatory effects of GG on dendritic cells, macrophages and monocytes from healthy donors publication-title: J Funct Foods – volume: 79 start-page: 305 issue: 5 year: 2014 end-page: 314 article-title: An optimized protocol for human M2 macrophages using M‐CSF and IL‐4/IL‐10/TGF‐β yields a dominant immunosuppressive phenotype publication-title: Scand J Immunol – volume: 13 start-page: 151 issue: 69 year: 2012 end-page: 158 article-title: Macrophage subpopulations in systemic lupus erythematosus publication-title: Discov Med – volume: 12 year: 2022 article-title: Bacteriocin‐producing probiotic lactic acid bacteria in controlling dysbiosis of the gut microbiota publication-title: Front Cell Infect Microbiol – volume: 56 start-page: i55 issue: suppl 1 year: 2017 end-page: i66 article-title: Pathways leading to an immunological disease: systemic lupus erythematosus publication-title: Rheumatology – volume: 244 year: 2022 article-title: Bidirectional crosstalk between dysbiotic gut microbiota and systemic lupus erythematosus: what is new in therapeutic approaches? publication-title: Clin Immunol – volume: 12 start-page: 12 year: 2021 article-title: The microbiota in systemic lupus erythematosus: an update on the potential function of probiotics publication-title: Front Pharmacol – volume: 21 start-page: 270 issue: 1 year: 2020 article-title: Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease publication-title: BMC Nephrol – volume: 22 start-page: 791 issue: 1 year: 2022 article-title: An M0 macrophage‐related prognostic model for hepatocellular carcinoma publication-title: BMC Cancer – volume: 2023 start-page: 1 year: 2023 end-page: 20 article-title: Regulatory mechanism of M1/M2 macrophage polarization in the development of autoimmune diseases publication-title: Mediators Inflamm – volume: 10 issue: 7 year: 2022 article-title: Paraprobiotics and postbiotics of CIDCA 133 mitigate 5‐FU‐induced intestinal inflammation publication-title: Microorganisms – volume: 65 start-page: 129 issue: 1 year: 1998 end-page: 138 article-title: Antitumour activity of yogurt: study of possible immune mechanisms publication-title: J Dairy Res – volume: 18 start-page: 90 issue: 1 year: 2016 article-title: CD163+ M2c‐like macrophages predominate in renal biopsies from patients with lupus nephritis publication-title: Arthritis Res Ther – volume: 52 start-page: 975 issue: 7 year: 2003 end-page: 980 article-title: Double blind, placebo controlled trial of two probiotic strains in interleukin 10 knockout mice and mechanistic link with cytokine balance publication-title: Gut – volume: 12 issue: 6 year: 2020 article-title: In vitro effects of live and heat‐inactivated subsp. , BB‐12 and GG on Caco‐2 cells publication-title: Nutrients – volume: 10 start-page: S17 issue: suppl 1 year: 2011 article-title: Immunomodulatory mechanisms of lactobacilli publication-title: Microb Cell Fact – volume: 13 issue: 12 year: 2018 article-title: Identification of alterations in macrophage activation associated with disease activity in systemic lupus erythematosus publication-title: PLoS One – volume: 17 start-page: 22508 issue: 22 year: 2023 end-page: 22526 article-title: Precisely regulating M2 subtype macrophages for renal fibrosis resolution publication-title: ACS Nano – volume: 16 start-page: 19 issue: 1 year: 2020 end-page: 30 article-title: Immunological pathogenesis and treatment of systemic lupus erythematosus publication-title: World J Pediatr – volume: 234 start-page: 9778 issue: 6 year: 2019 end-page: 9786 article-title: Amelioration of regulatory T cells by and in pristane‐induced lupus mice model publication-title: J Cell Physiol – volume: 10 start-page: 1047 year: 2019 article-title: Emerging health concepts in the probiotics field: streamlining the definitions publication-title: Front Microbiol – volume: 207 start-page: 53 issue: 1 year: 2021 end-page: 64 article-title: The effect of short‐chain fatty acids on M2 macrophages polarization in vitro and in vivo publication-title: Clin Exp Immunol – volume: 8 year: 2017 article-title: Regulation of human macrophage M1‐M2 polarization balance by hypoxia and the triggering receptor expressed on myeloid cells‐1 publication-title: Front Immunol – volume: 195 start-page: 4660 issue: 10 year: 2015 end-page: 4667 article-title: A central role for HLA‐DR3 in anti‐smith antibody responses and glomerulonephritis in a transgenic mouse model of spontaneous lupus publication-title: J Immunol – volume: 49 start-page: 82 issue: 1 year: 1999 end-page: 87 article-title: Differential expression and modulation of costimulatory molecules CD80 and CD86 on monocytes from patients with systemic lupus erythematosus publication-title: Scand J Immunol – volume: 7 issue: 8 year: 2012 article-title: In vitro generation of monocyte‐derived macrophages under serum‐free conditions improves their tumor promoting functions publication-title: PLoS One – volume: 5 start-page: 514 year: 2014 article-title: From monocytes to M1/M2 macrophages: phenotypical vs. functional differentiation publication-title: Front Immunol – volume: 48 start-page: 228 year: 2018 end-page: 233 article-title: and ameliorate the expression of miR‐155 and miR‐181a in SLE patients publication-title: J Funct Foods – volume: 2019 start-page: 10 year: 2019 article-title: Monocyte differentiation and macrophage polarization publication-title: Vessel Plus – volume: 12 year: 2021 article-title: Macrophage polarization and plasticity in systemic lupus erythematosus publication-title: Front Immunol – volume: 10 start-page: 772 year: 2019 article-title: Innate immune cells' contribution to systemic lupus erythematosus publication-title: Front Immunol – volume: 154 year: 2022 article-title: SARS‐CoV‐2 triggering autoimmune diseases publication-title: Cytokine – volume: 127 start-page: 303 issue: 2 year: 2011 end-page: 312 article-title: Current and novel therapeutics in the treatment of systemic lupus erythematosus publication-title: J Allergy Clin Immunol – volume: 16 start-page: 79 issue: 1 year: 2017 article-title: Beneficial effects on host energy metabolism of short‐chain fatty acids and vitamins produced by commensal and probiotic bacteria publication-title: Microb Cell Fact – ident: e_1_2_11_6_1 doi: 10.1093/rheumatology/kew427 – ident: e_1_2_11_7_1 doi: 10.1016/j.cell.2010.02.029 – ident: e_1_2_11_67_1 doi: 10.1186/s12882-020-01921-7 – ident: e_1_2_11_87_1 doi: 10.3389/fimmu.2017.01063 – ident: e_1_2_11_74_1 doi: 10.3389/fimmu.2017.01097 – ident: e_1_2_11_58_1 doi: 10.1046/j.1365-3083.1999.00452.x – ident: e_1_2_11_29_1 doi: 10.1186/1475-2859-10-S1-S17 – ident: e_1_2_11_23_1 doi: 10.1186/s13075-016-0989-y – ident: e_1_2_11_44_1 doi: 10.3109/02652048.2015.1057249 – ident: e_1_2_11_32_1 doi: 10.3389/fnut.2022.931458 – ident: e_1_2_11_69_1 doi: 10.21203/rs.3.rs-49282/v1 – ident: e_1_2_11_5_1 doi: 10.1038/s41584-021-00668-1 – volume: 18 start-page: 1683 issue: 10 year: 2008 ident: e_1_2_11_80_1 article-title: Antiinflammatory effect of lactic acid bacteria: inhibition of cyclooxygenase‐2 by suppressing nuclear factor‐κB in Raw264.7 macrophage cells publication-title: J Microbiol Biotechnol – ident: e_1_2_11_83_1 doi: 10.1093/cei/uxab028 – ident: e_1_2_11_28_1 doi: 10.1002/jcp.25748 – ident: e_1_2_11_11_1 doi: 10.1007/s12032-020-01435-0 – ident: e_1_2_11_37_1 doi: 10.3389/fphar.2021.759095 – ident: e_1_2_11_9_1 doi: 10.3389/fimmu.2016.00035 – ident: e_1_2_11_38_1 doi: 10.1016/j.afres.2022.100185 – ident: e_1_2_11_35_1 doi: 10.3390/microorganisms10071418 – ident: e_1_2_11_40_1 doi: 10.1007/978-3-030-55035-6_6 – ident: e_1_2_11_72_1 doi: 10.1136/annrheumdis-2018-214333 – ident: e_1_2_11_62_1 doi: 10.1101/2022.06.13.495868 – volume: 8 start-page: 235 issue: 3 year: 2016 ident: e_1_2_11_15_1 article-title: The role of HPaA protein as candidate vaccine against Helicobacter pylori publication-title: Der Pharma Chem – ident: e_1_2_11_25_1 doi: 10.1093/ndt/gfy195 – ident: e_1_2_11_36_1 doi: 10.1007/s13213-015-1093-2 – ident: e_1_2_11_90_1 doi: 10.1136/gut.2003.037325 – ident: e_1_2_11_8_1 doi: 10.3389/fimmu.2019.00772 – ident: e_1_2_11_84_1 – volume: 13 start-page: 13 year: 2022 ident: e_1_2_11_85_1 article-title: Lactate‐driven macrophage polarization in the inflammatory microenvironment alleviates intestinal inflammation publication-title: Front Immunol – ident: e_1_2_11_60_1 doi: 10.4049/jimmunol.1501073 – ident: e_1_2_11_73_1 doi: 10.3389/fimmu.2014.00514 – ident: e_1_2_11_4_1 doi: 10.1002/jcb.26155 – ident: e_1_2_11_17_1 doi: 10.1016/j.cellsig.2013.11.004 – ident: e_1_2_11_79_1 doi: 10.1007/s12602-019-09612-y – ident: e_1_2_11_14_1 doi: 10.1186/s12885-022-09872-y – ident: e_1_2_11_22_1 doi: 10.1155/2023/8821610 – ident: e_1_2_11_39_1 doi: 10.1111/jam.12521 – ident: e_1_2_11_43_1 doi: 10.1111/j.1440-1746.2008.05723.x – ident: e_1_2_11_82_1 doi: 10.1186/s12934-017-0691-z – volume: 13 start-page: 151 issue: 69 year: 2012 ident: e_1_2_11_18_1 article-title: Macrophage subpopulations in systemic lupus erythematosus publication-title: Discov Med – ident: e_1_2_11_26_1 doi: 10.1021/acsnano.3c05998 – ident: e_1_2_11_78_1 doi: 10.1155/2018/1756308 – ident: e_1_2_11_10_1 doi: 10.1371/journal.pone.0090972 – ident: e_1_2_11_20_1 doi: 10.1089/scd.2023.0047 – volume: 24 start-page: 1509 issue: 11 year: 2021 ident: e_1_2_11_52_1 article-title: Inhibitory effects of tolerogenic probiotics on migratory potential of lupus patient‐derived DCs publication-title: Iran J Basic Med Sci – ident: e_1_2_11_34_1 doi: 10.3390/nu12061719 – ident: e_1_2_11_66_1 doi: 10.1371/journal.pone.0042656 – ident: e_1_2_11_86_1 doi: 10.3389/fcimb.2022.851140 – ident: e_1_2_11_27_1 doi: 10.3389/fmicb.2019.01047 – ident: e_1_2_11_65_1 doi: 10.3389/fphar.2018.00071 – ident: e_1_2_11_81_1 doi: 10.1016/j.intimp.2022.108983 – ident: e_1_2_11_70_1 doi: 10.3390/biom11060837 – ident: e_1_2_11_31_1 doi: 10.1002/ibd.21834 – ident: e_1_2_11_51_1 doi: 10.1002/jcp.27663 – ident: e_1_2_11_89_1 doi: 10.1136/gut.52.7.975 – ident: e_1_2_11_12_1 doi: 10.1371/journal.pone.0208132 – ident: e_1_2_11_56_1 doi: 10.1016/j.clim.2022.109109 – ident: e_1_2_11_42_1 doi: 10.1016/j.jff.2018.07.025 – ident: e_1_2_11_53_1 doi: 10.1371/journal.pone.0085923 – ident: e_1_2_11_19_1 doi: 10.4049/jimmunol.1002315 – ident: e_1_2_11_46_1 doi: 10.1111/sji.12162 – ident: e_1_2_11_50_1 doi: 10.1016/j.jaci.2010.12.1087 – ident: e_1_2_11_59_1 doi: 10.1016/j.humimm.2004.01.005 – ident: e_1_2_11_75_1 doi: 10.1016/j.nut.2018.02.005 – ident: e_1_2_11_3_1 doi: 10.1007/s12519-019-00229-3 – ident: e_1_2_11_54_1 doi: 10.1371/journal.pone.0008668 – ident: e_1_2_11_47_1 doi: 10.1016/j.cyto.2022.155873 – ident: e_1_2_11_30_1 doi: 10.3390/foods12040692 – ident: e_1_2_11_88_1 doi: 10.1080/20013078.2020.1793514 – ident: e_1_2_11_68_1 doi: 10.3389/fonc.2019.01512 – ident: e_1_2_11_24_1 doi: 10.1016/j.jaut.2019.01.004 – ident: e_1_2_11_63_1 doi: 10.1016/j.molimm.2017.05.027 – ident: e_1_2_11_55_1 doi: 10.1016/B0-12-370879-6/00063-6 – ident: e_1_2_11_57_1 doi: 10.1191/0961203302lu201oa – ident: e_1_2_11_41_1 doi: 10.1016/j.jff.2014.12.040 – ident: e_1_2_11_49_1 doi: 10.3389/fimmu.2021.734008 – volume: 2 start-page: 93 issue: 1 year: 2007 ident: e_1_2_11_61_1 article-title: Immunopathogenesis of systemic lupus erythematosus publication-title: Int J Clin Rheumatol – ident: e_1_2_11_2_1 doi: 10.1002/jcb.27203 – ident: e_1_2_11_21_1 doi: 10.3389/fimmu.2022.913007 – ident: e_1_2_11_64_1 doi: 10.1038/s41598-017-08121-8 – volume: 20 start-page: 43 issue: 108 year: 2015 ident: e_1_2_11_16_1 article-title: Therapeutic targeting of macrophages in lupus nephritis publication-title: Discov Med – ident: e_1_2_11_77_1 doi: 10.1017/S0022029997002604 – ident: e_1_2_11_13_1 doi: 10.3389/fimmu.2014.00603 – ident: e_1_2_11_33_1 doi: 10.1007/s12602-021-09842-z – ident: e_1_2_11_76_1 doi: 10.1016/j.crfs.2020.02.002 – ident: e_1_2_11_71_1 doi: 10.20517/2574-1209.2019.04 – ident: e_1_2_11_45_1 doi: 10.1002/jcp.26819 – ident: e_1_2_11_48_1 doi: 10.1007/s11926-017-0708-y |
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Snippet | Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self‐tolerance, resulting in disease onset and... Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self-tolerance, resulting in disease onset and... |
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SubjectTerms | Anti-Inflammatory Agents - pharmacology Antigens Autoimmune diseases CD14 antigen CD80 antigen Chronic conditions Clusters Cytokines Cytokines - metabolism Differentiation Flow cytometry Growth factors Histocompatibility antigen HLA Humans Immunological tolerance Immunomodulation Inflammation Interleukin-10 Interleukin-12 - metabolism Interleukin-12 - pharmacology Interleukin-12 - therapeutic use Interleukins Lacticaseibacillus rhamnosus Lactobacilli Lactobacillus delbrueckii Lactobacillus delbrueckii - metabolism Lactobacillus rhamnosus Leukocytes Lipopolysaccharides Lipopolysaccharides - pharmacology Lupus Lupus Erythematosus, Systemic - drug therapy M0/M1/M2 macrophages macrophage Macrophages Macrophages - metabolism Monocytes Monocytes - metabolism Monocytes - pathology Patients Phagocytosis Polymerase chain reaction probiotic Probiotics Probiotics - pharmacology Systemic lupus erythematosus Transforming Growth Factor beta - metabolism Transforming growth factor-b Tumor Necrosis Factor-alpha - metabolism Tumor necrosis factor-TNF Tumor necrosis factor-α |
Title | Tolerogenic probiotics Lactobacillus delbrueckii and Lactobacillus rhamnosus promote anti‐inflammatory profile of macrophages‐derived monocytes of newly diagnosed patients with systemic lupus erythematosus |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcbf.3981 https://www.ncbi.nlm.nih.gov/pubmed/38509733 https://www.proquest.com/docview/2986770128 https://www.proquest.com/docview/2973101856 |
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