Modification of phagocytosis and cytokine production in peritoneal and splenic murine cells by erythromycin A, azithromycin and josamycin
Objectives: The aim of this study was to determine whether pre-incubation of peritoneal or splenic cells with different doses of the macrolides erythromycin A (14-membered ring), azithromycin (15-membered ring) and josamycin (16-membered ring) affects their phagocytic activity or cytokine production...
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Veröffentlicht in: | Journal of antimicrobial chemotherapy 2004-02, Vol.53 (2), p.367-370 |
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creator | Ortega, Elena Escobar, M. Antonia Gaforio, José Juan Algarra, Ignacio Alvarez de Cienfuegos, Gerardo |
description | Objectives: The aim of this study was to determine whether pre-incubation of peritoneal or splenic cells with different doses of the macrolides erythromycin A (14-membered ring), azithromycin (15-membered ring) and josamycin (16-membered ring) affects their phagocytic activity or cytokine production. Methods: Peritoneal and splenic cells from BALB/c mice were pre-incubated with different concentrations of these antibiotics, those similar to serum levels attained with the treatment schedules used in human therapy. Results: From our observations of phagocytic activity and IL-12 production by peritoneal cells, these macrolide antibiotics seem to act mainly as immunosuppressive agents, although they induce peritoneal cells to increase IL-18 production and splenic cells IL-4 production. Conclusions: Macrolide antibiotics can interfere with the Th1 cell-amplifying activity of IL-18 in conjunction with IL-12 and, in contrast, may induce a Th2 cell response in an IL-4-dependent manner. These results could improve their therapeutic use especially in immunosuppressed patients. |
doi_str_mv | 10.1093/jac/dkh069 |
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Antonia ; Gaforio, José Juan ; Algarra, Ignacio ; Alvarez de Cienfuegos, Gerardo</creator><creatorcontrib>Ortega, Elena ; Escobar, M. Antonia ; Gaforio, José Juan ; Algarra, Ignacio ; Alvarez de Cienfuegos, Gerardo</creatorcontrib><description>Objectives: The aim of this study was to determine whether pre-incubation of peritoneal or splenic cells with different doses of the macrolides erythromycin A (14-membered ring), azithromycin (15-membered ring) and josamycin (16-membered ring) affects their phagocytic activity or cytokine production. Methods: Peritoneal and splenic cells from BALB/c mice were pre-incubated with different concentrations of these antibiotics, those similar to serum levels attained with the treatment schedules used in human therapy. Results: From our observations of phagocytic activity and IL-12 production by peritoneal cells, these macrolide antibiotics seem to act mainly as immunosuppressive agents, although they induce peritoneal cells to increase IL-18 production and splenic cells IL-4 production. Conclusions: Macrolide antibiotics can interfere with the Th1 cell-amplifying activity of IL-18 in conjunction with IL-12 and, in contrast, may induce a Th2 cell response in an IL-4-dependent manner. These results could improve their therapeutic use especially in immunosuppressed patients.</description><identifier>ISSN: 0305-7453</identifier><identifier>ISSN: 1460-2091</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkh069</identifier><identifier>PMID: 14729765</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animals ; Anti-Bacterial Agents - pharmacology ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Azithromycin - pharmacology ; Biological and medical sciences ; Candida albicans - immunology ; Cytokines - biosynthesis ; Enzyme-Linked Immunosorbent Assay ; Erythromycin - pharmacology ; IL-12 ; IL-18 ; IL-4 ; immunomodulation ; In Vitro Techniques ; Interleukin-12 - biosynthesis ; Interleukin-18 - biosynthesis ; Interleukin-4 - biosynthesis ; Josamycin - pharmacology ; macrolide antibiotics ; Macrophages, Peritoneal - drug effects ; Macrophages, Peritoneal - metabolism ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Phagocytosis - drug effects ; Pharmacology. 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Antonia</creatorcontrib><creatorcontrib>Gaforio, José Juan</creatorcontrib><creatorcontrib>Algarra, Ignacio</creatorcontrib><creatorcontrib>Alvarez de Cienfuegos, Gerardo</creatorcontrib><title>Modification of phagocytosis and cytokine production in peritoneal and splenic murine cells by erythromycin A, azithromycin and josamycin</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J. Antimicrob. Chemother</addtitle><description>Objectives: The aim of this study was to determine whether pre-incubation of peritoneal or splenic cells with different doses of the macrolides erythromycin A (14-membered ring), azithromycin (15-membered ring) and josamycin (16-membered ring) affects their phagocytic activity or cytokine production. Methods: Peritoneal and splenic cells from BALB/c mice were pre-incubated with different concentrations of these antibiotics, those similar to serum levels attained with the treatment schedules used in human therapy. Results: From our observations of phagocytic activity and IL-12 production by peritoneal cells, these macrolide antibiotics seem to act mainly as immunosuppressive agents, although they induce peritoneal cells to increase IL-18 production and splenic cells IL-4 production. Conclusions: Macrolide antibiotics can interfere with the Th1 cell-amplifying activity of IL-18 in conjunction with IL-12 and, in contrast, may induce a Th2 cell response in an IL-4-dependent manner. These results could improve their therapeutic use especially in immunosuppressed patients.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Azithromycin - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Candida albicans - immunology</subject><subject>Cytokines - biosynthesis</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Erythromycin - pharmacology</subject><subject>IL-12</subject><subject>IL-18</subject><subject>IL-4</subject><subject>immunomodulation</subject><subject>In Vitro Techniques</subject><subject>Interleukin-12 - biosynthesis</subject><subject>Interleukin-18 - biosynthesis</subject><subject>Interleukin-4 - biosynthesis</subject><subject>Josamycin - pharmacology</subject><subject>macrolide antibiotics</subject><subject>Macrophages, Peritoneal - drug effects</subject><subject>Macrophages, Peritoneal - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Phagocytosis - drug effects</subject><subject>Pharmacology. Drug treatments</subject><subject>Spleen - cytology</subject><subject>Spleen - drug effects</subject><subject>Spleen - metabolism</subject><issn>0305-7453</issn><issn>1460-2091</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0UFvFCEUAGBiNHatXvwBhpjowTgWFgaGY9PY1qSNMWrSeCFvgXHZnRlGmEkc_0H_tczuppv0Ao_wPXjwEHpNySdKFDvbgDmz2zUR6glaUC5IsSSKPkULwkhZSF6yE_QipQ0hRJSieo5OKJdLJUW5QPe3wfraGxh86HCocb-G38FMQ0g-YegsnuOt7xzuY7Cj2Tnf4d5FP4TOQbNTqW9c5w1uxzhb45om4dWEXZyGdQztZHLO-UcM__xxPSduQoLd6iV6VkOT3KvDfIp-Xn7-cXFd3Hy9-nJxflMYTvkwj86KUjGgzNVLVVbUSSEALLPUrRyvqRS1yiEDUXGiwNbKSqsUFfmHVuwUvd-fm9_zZ3Rp0K1Pc73QuTAmXRHKGZUyw7eP4CaMscu16WW-o5JczejDHpkYUoqu1n30LcRJU6Ln7ujcHb3vTsZvDieOq9bZIz20I4N3BwDJQFNH6IxPR1fyqpRydsXe-TS4vw_7ELdaSCZLfX33S19efefk7lsug_0H42KqlQ</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Ortega, Elena</creator><creator>Escobar, M. 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Antonia ; Gaforio, José Juan ; Algarra, Ignacio ; Alvarez de Cienfuegos, Gerardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-c41ed6593a13ef29581e766aad3d1ebe4f176f91eb3a68409adf9d7d9916069b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Azithromycin - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Candida albicans - immunology</topic><topic>Cytokines - biosynthesis</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Erythromycin - pharmacology</topic><topic>IL-12</topic><topic>IL-18</topic><topic>IL-4</topic><topic>immunomodulation</topic><topic>In Vitro Techniques</topic><topic>Interleukin-12 - biosynthesis</topic><topic>Interleukin-18 - biosynthesis</topic><topic>Interleukin-4 - biosynthesis</topic><topic>Josamycin - pharmacology</topic><topic>macrolide antibiotics</topic><topic>Macrophages, Peritoneal - drug effects</topic><topic>Macrophages, Peritoneal - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Phagocytosis - drug effects</topic><topic>Pharmacology. 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Antonia</au><au>Gaforio, José Juan</au><au>Algarra, Ignacio</au><au>Alvarez de Cienfuegos, Gerardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modification of phagocytosis and cytokine production in peritoneal and splenic murine cells by erythromycin A, azithromycin and josamycin</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J. Antimicrob. Chemother</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>53</volume><issue>2</issue><spage>367</spage><epage>370</epage><pages>367-370</pages><issn>0305-7453</issn><issn>1460-2091</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Objectives: The aim of this study was to determine whether pre-incubation of peritoneal or splenic cells with different doses of the macrolides erythromycin A (14-membered ring), azithromycin (15-membered ring) and josamycin (16-membered ring) affects their phagocytic activity or cytokine production. Methods: Peritoneal and splenic cells from BALB/c mice were pre-incubated with different concentrations of these antibiotics, those similar to serum levels attained with the treatment schedules used in human therapy. Results: From our observations of phagocytic activity and IL-12 production by peritoneal cells, these macrolide antibiotics seem to act mainly as immunosuppressive agents, although they induce peritoneal cells to increase IL-18 production and splenic cells IL-4 production. Conclusions: Macrolide antibiotics can interfere with the Th1 cell-amplifying activity of IL-18 in conjunction with IL-12 and, in contrast, may induce a Th2 cell response in an IL-4-dependent manner. These results could improve their therapeutic use especially in immunosuppressed patients.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>14729765</pmid><doi>10.1093/jac/dkh069</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anti-Bacterial Agents - pharmacology Antibiotics. Antiinfectious agents. Antiparasitic agents Azithromycin - pharmacology Biological and medical sciences Candida albicans - immunology Cytokines - biosynthesis Enzyme-Linked Immunosorbent Assay Erythromycin - pharmacology IL-12 IL-18 IL-4 immunomodulation In Vitro Techniques Interleukin-12 - biosynthesis Interleukin-18 - biosynthesis Interleukin-4 - biosynthesis Josamycin - pharmacology macrolide antibiotics Macrophages, Peritoneal - drug effects Macrophages, Peritoneal - metabolism Male Medical sciences Mice Mice, Inbred BALB C Phagocytosis - drug effects Pharmacology. Drug treatments Spleen - cytology Spleen - drug effects Spleen - metabolism |
title | Modification of phagocytosis and cytokine production in peritoneal and splenic murine cells by erythromycin A, azithromycin and josamycin |
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