Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig
► Mw induces differential expression of CXCL10 and CXCL11 in TB infections. ► Chemokines are expressed in MTB infection with/without therapeutic interventions. ► Mw alone also can provide partial protection against tuberculosis. ► RvChMw group has less CFU for entire study period. ► Mw with combinat...
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creator | Rawat, Krishna Dutta Chahar, Mamta Reddy, P.V.J. Gupta, Pushpa Shrivastava, Nalini Gupta, U.D. Natrajan, M. Katoch, V.M. Katoch, Kiran Chauhan, D.S. |
description | ► Mw induces differential expression of CXCL10 and CXCL11 in TB infections. ► Chemokines are expressed in MTB infection with/without therapeutic interventions. ► Mw alone also can provide partial protection against tuberculosis. ► RvChMw group has less CFU for entire study period. ► Mw with combination of chemotherapy showed better results.
Mycobacterium indicus pranii (earlier known as Mycobacterium w) has been used as an immunmodulatory agent in leprosy and tuberculosis by mediating the release of various cytokines and chemokines. CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines are involved in T-cell migration and stimulation of natural killer cells in Mycobacterium tuberculosis infection. In this study, the effect of heat killed M. indicus pranii (alone and in conjunction with chemotherapy) on disease progression was determined by colony forming units (CFUs) in guinea pig lung following their aerosol infection and the expression levels of CXCL10 and CXCL11 were studied by quantitative Reverse Transcriptase Polymerase Chain Reaction (qRT-PCR) and in situ RT-PCR. Four groups of animals included; infection only (Rv), immunoprophylaxis (RvMw), chemotherapy (RvCh) and combination of immunoprophylaxis with chemotherapy (RvChMw). In the group where immunoprophylaxis was given in combination with chemotherapy, the CFU counts reduced significantly at 4th week post-infection as compared to animals that received immunoprophylaxis or chemotherapy alone. At the same time, all groups of animals had elevated expression of CXCL 10 which was significantly high only in animals that received Mw with or without chemotherapy. Unlike to CXCL 10, study demonstrated suppressed expression CXCL 11 in both immunoprophylaxis as well as chemotherapy groups that became up-regulated in synergistic response of immunoprophylaxis and chemotherapy. Taken together, data indicates that the expression of CXCL10 and CXCL11 positively correlates with anti-tubercular treatment (at least with combination of immunoprophylaxis and chemotherapy). Therefore, prior immunization with Mw appears to be a good immunomodulator for release of chemokines and augments the effect of chemotherapy. |
doi_str_mv | 10.1016/j.meegid.2012.10.002 |
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Mycobacterium indicus pranii (earlier known as Mycobacterium w) has been used as an immunmodulatory agent in leprosy and tuberculosis by mediating the release of various cytokines and chemokines. CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines are involved in T-cell migration and stimulation of natural killer cells in Mycobacterium tuberculosis infection. In this study, the effect of heat killed M. indicus pranii (alone and in conjunction with chemotherapy) on disease progression was determined by colony forming units (CFUs) in guinea pig lung following their aerosol infection and the expression levels of CXCL10 and CXCL11 were studied by quantitative Reverse Transcriptase Polymerase Chain Reaction (qRT-PCR) and in situ RT-PCR. Four groups of animals included; infection only (Rv), immunoprophylaxis (RvMw), chemotherapy (RvCh) and combination of immunoprophylaxis with chemotherapy (RvChMw). In the group where immunoprophylaxis was given in combination with chemotherapy, the CFU counts reduced significantly at 4th week post-infection as compared to animals that received immunoprophylaxis or chemotherapy alone. At the same time, all groups of animals had elevated expression of CXCL 10 which was significantly high only in animals that received Mw with or without chemotherapy. Unlike to CXCL 10, study demonstrated suppressed expression CXCL 11 in both immunoprophylaxis as well as chemotherapy groups that became up-regulated in synergistic response of immunoprophylaxis and chemotherapy. Taken together, data indicates that the expression of CXCL10 and CXCL11 positively correlates with anti-tubercular treatment (at least with combination of immunoprophylaxis and chemotherapy). Therefore, prior immunization with Mw appears to be a good immunomodulator for release of chemokines and augments the effect of chemotherapy.</description><identifier>ISSN: 1567-1348</identifier><identifier>EISSN: 1567-7257</identifier><identifier>DOI: 10.1016/j.meegid.2012.10.002</identifier><identifier>PMID: 23107775</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Bacterial Load ; Chemokine CXCL10 - genetics ; Chemokine CXCL11 - genetics ; Chemokines ; CXCL10 ; CXCL11 ; Gene Expression ; Guinea Pigs ; Immunoprophylaxis ; Lung - metabolism ; Lung - microbiology ; Lung - pathology ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - immunology ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Time Factors ; Tuberculosis - genetics ; Tuberculosis - microbiology ; Tuberculosis - prevention & control</subject><ispartof>Infection, genetics and evolution, 2013-01, Vol.13, p.11-17</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-b7a5524e6b064ad5605ae5b0459b3bfd71a7d939325406b046dd11ae2e90d30b3</citedby><cites>FETCH-LOGICAL-c362t-b7a5524e6b064ad5605ae5b0459b3bfd71a7d939325406b046dd11ae2e90d30b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1567134812003255$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23107775$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rawat, Krishna Dutta</creatorcontrib><creatorcontrib>Chahar, Mamta</creatorcontrib><creatorcontrib>Reddy, P.V.J.</creatorcontrib><creatorcontrib>Gupta, Pushpa</creatorcontrib><creatorcontrib>Shrivastava, Nalini</creatorcontrib><creatorcontrib>Gupta, U.D.</creatorcontrib><creatorcontrib>Natrajan, M.</creatorcontrib><creatorcontrib>Katoch, V.M.</creatorcontrib><creatorcontrib>Katoch, Kiran</creatorcontrib><creatorcontrib>Chauhan, D.S.</creatorcontrib><title>Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig</title><title>Infection, genetics and evolution</title><addtitle>Infect Genet Evol</addtitle><description>► Mw induces differential expression of CXCL10 and CXCL11 in TB infections. ► Chemokines are expressed in MTB infection with/without therapeutic interventions. ► Mw alone also can provide partial protection against tuberculosis. ► RvChMw group has less CFU for entire study period. ► Mw with combination of chemotherapy showed better results.
Mycobacterium indicus pranii (earlier known as Mycobacterium w) has been used as an immunmodulatory agent in leprosy and tuberculosis by mediating the release of various cytokines and chemokines. CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines are involved in T-cell migration and stimulation of natural killer cells in Mycobacterium tuberculosis infection. In this study, the effect of heat killed M. indicus pranii (alone and in conjunction with chemotherapy) on disease progression was determined by colony forming units (CFUs) in guinea pig lung following their aerosol infection and the expression levels of CXCL10 and CXCL11 were studied by quantitative Reverse Transcriptase Polymerase Chain Reaction (qRT-PCR) and in situ RT-PCR. Four groups of animals included; infection only (Rv), immunoprophylaxis (RvMw), chemotherapy (RvCh) and combination of immunoprophylaxis with chemotherapy (RvChMw). In the group where immunoprophylaxis was given in combination with chemotherapy, the CFU counts reduced significantly at 4th week post-infection as compared to animals that received immunoprophylaxis or chemotherapy alone. At the same time, all groups of animals had elevated expression of CXCL 10 which was significantly high only in animals that received Mw with or without chemotherapy. Unlike to CXCL 10, study demonstrated suppressed expression CXCL 11 in both immunoprophylaxis as well as chemotherapy groups that became up-regulated in synergistic response of immunoprophylaxis and chemotherapy. Taken together, data indicates that the expression of CXCL10 and CXCL11 positively correlates with anti-tubercular treatment (at least with combination of immunoprophylaxis and chemotherapy). Therefore, prior immunization with Mw appears to be a good immunomodulator for release of chemokines and augments the effect of chemotherapy.</description><subject>Animals</subject><subject>Bacterial Load</subject><subject>Chemokine CXCL10 - genetics</subject><subject>Chemokine CXCL11 - genetics</subject><subject>Chemokines</subject><subject>CXCL10</subject><subject>CXCL11</subject><subject>Gene Expression</subject><subject>Guinea Pigs</subject><subject>Immunoprophylaxis</subject><subject>Lung - metabolism</subject><subject>Lung - microbiology</subject><subject>Lung - pathology</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - immunology</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Time Factors</subject><subject>Tuberculosis - genetics</subject><subject>Tuberculosis - microbiology</subject><subject>Tuberculosis - prevention & control</subject><issn>1567-1348</issn><issn>1567-7257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcuO0zAUjRCIecAfIORlu0ixnTiebpBG0TCM1BEsBomd5di37S1JHOx4ZvpZ_CGOUliwYGHZOj6Pa58se8foilFWfTisOoAd2hWnjCdoRSl_kZ0zUclcciFfns6sKK_OsosQDpQySfnV6-yMF4xKKcV59uvmefAQArqeuC2pv9cbRsni7mvO6JLo3s4QS1D-cF0vidlD535gD4HY6LHfkfujcY02I3iMHRljA97E1gUMBPstmHHynpyw62LvBu-G_bHVz-n-Ccf9P3rsLZoYyOB1j0gW90_LhJFdTJGaDLh7k73a6jbA29N-mX37dPNQf843X27v6utNboqKj3kjtRC8hKqhVamtqKjQIBpainVTNFsrmZZ2XawLLkqaSGVlLWMaOKypLWhTXGaL2TcN_DNCGFWHwUDb6h5cDIpxWXCaFk_UcqYa70LwsFWDx077o2JUTWWpg5rLUlNZE5rKSrL3p4TYdGD_iv60kwgfZwKkdz4ieBUMQm_Aok__qqzD_yf8BrKep4U</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Rawat, Krishna Dutta</creator><creator>Chahar, Mamta</creator><creator>Reddy, P.V.J.</creator><creator>Gupta, Pushpa</creator><creator>Shrivastava, Nalini</creator><creator>Gupta, U.D.</creator><creator>Natrajan, M.</creator><creator>Katoch, V.M.</creator><creator>Katoch, Kiran</creator><creator>Chauhan, D.S.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201301</creationdate><title>Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig</title><author>Rawat, Krishna Dutta ; Chahar, Mamta ; Reddy, P.V.J. ; Gupta, Pushpa ; Shrivastava, Nalini ; Gupta, U.D. ; Natrajan, M. ; Katoch, V.M. ; Katoch, Kiran ; Chauhan, D.S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-b7a5524e6b064ad5605ae5b0459b3bfd71a7d939325406b046dd11ae2e90d30b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Bacterial Load</topic><topic>Chemokine CXCL10 - genetics</topic><topic>Chemokine CXCL11 - genetics</topic><topic>Chemokines</topic><topic>CXCL10</topic><topic>CXCL11</topic><topic>Gene Expression</topic><topic>Guinea Pigs</topic><topic>Immunoprophylaxis</topic><topic>Lung - metabolism</topic><topic>Lung - microbiology</topic><topic>Lung - pathology</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - immunology</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Time Factors</topic><topic>Tuberculosis - genetics</topic><topic>Tuberculosis - microbiology</topic><topic>Tuberculosis - prevention & control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rawat, Krishna Dutta</creatorcontrib><creatorcontrib>Chahar, Mamta</creatorcontrib><creatorcontrib>Reddy, P.V.J.</creatorcontrib><creatorcontrib>Gupta, Pushpa</creatorcontrib><creatorcontrib>Shrivastava, Nalini</creatorcontrib><creatorcontrib>Gupta, U.D.</creatorcontrib><creatorcontrib>Natrajan, M.</creatorcontrib><creatorcontrib>Katoch, V.M.</creatorcontrib><creatorcontrib>Katoch, Kiran</creatorcontrib><creatorcontrib>Chauhan, D.S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Infection, genetics and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rawat, Krishna Dutta</au><au>Chahar, Mamta</au><au>Reddy, P.V.J.</au><au>Gupta, Pushpa</au><au>Shrivastava, Nalini</au><au>Gupta, U.D.</au><au>Natrajan, M.</au><au>Katoch, V.M.</au><au>Katoch, Kiran</au><au>Chauhan, D.S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig</atitle><jtitle>Infection, genetics and evolution</jtitle><addtitle>Infect Genet Evol</addtitle><date>2013-01</date><risdate>2013</risdate><volume>13</volume><spage>11</spage><epage>17</epage><pages>11-17</pages><issn>1567-1348</issn><eissn>1567-7257</eissn><abstract>► Mw induces differential expression of CXCL10 and CXCL11 in TB infections. ► Chemokines are expressed in MTB infection with/without therapeutic interventions. ► Mw alone also can provide partial protection against tuberculosis. ► RvChMw group has less CFU for entire study period. ► Mw with combination of chemotherapy showed better results.
Mycobacterium indicus pranii (earlier known as Mycobacterium w) has been used as an immunmodulatory agent in leprosy and tuberculosis by mediating the release of various cytokines and chemokines. CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines are involved in T-cell migration and stimulation of natural killer cells in Mycobacterium tuberculosis infection. In this study, the effect of heat killed M. indicus pranii (alone and in conjunction with chemotherapy) on disease progression was determined by colony forming units (CFUs) in guinea pig lung following their aerosol infection and the expression levels of CXCL10 and CXCL11 were studied by quantitative Reverse Transcriptase Polymerase Chain Reaction (qRT-PCR) and in situ RT-PCR. Four groups of animals included; infection only (Rv), immunoprophylaxis (RvMw), chemotherapy (RvCh) and combination of immunoprophylaxis with chemotherapy (RvChMw). In the group where immunoprophylaxis was given in combination with chemotherapy, the CFU counts reduced significantly at 4th week post-infection as compared to animals that received immunoprophylaxis or chemotherapy alone. At the same time, all groups of animals had elevated expression of CXCL 10 which was significantly high only in animals that received Mw with or without chemotherapy. Unlike to CXCL 10, study demonstrated suppressed expression CXCL 11 in both immunoprophylaxis as well as chemotherapy groups that became up-regulated in synergistic response of immunoprophylaxis and chemotherapy. Taken together, data indicates that the expression of CXCL10 and CXCL11 positively correlates with anti-tubercular treatment (at least with combination of immunoprophylaxis and chemotherapy). Therefore, prior immunization with Mw appears to be a good immunomodulator for release of chemokines and augments the effect of chemotherapy.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23107775</pmid><doi>10.1016/j.meegid.2012.10.002</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Bacterial Load Chemokine CXCL10 - genetics Chemokine CXCL11 - genetics Chemokines CXCL10 CXCL11 Gene Expression Guinea Pigs Immunoprophylaxis Lung - metabolism Lung - microbiology Lung - pathology Mycobacterium tuberculosis Mycobacterium tuberculosis - immunology RNA, Messenger - genetics RNA, Messenger - metabolism Time Factors Tuberculosis - genetics Tuberculosis - microbiology Tuberculosis - prevention & control |
title | Expression of CXCL10 (IP-10) and CXCL11 (I-TAC) chemokines during Mycobacterium tuberculosis infection and immunoprophylaxis with Mycobacterium indicus pranii (Mw) in guinea pig |
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