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Tumor necrosis factor-alpha and interleukin-10 in whole blood is associated with disease progression in pulmonary multidrug-resistant tuberculosis patients

DC Field Value Language
dc.contributor.author조상래-
dc.date.accessioned2015-05-19T17:06:07Z-
dc.date.available2015-05-19T17:06:07Z-
dc.date.issued2008-
dc.identifier.issn0025-7931-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/107508-
dc.description.abstractBACKGROUND: Cytokine production profiles may reflect the clinical pictures of patients with tuberculosis (TB). OBJECTIVE: We examined the relationship between cytokine levels and clinical parameters indicating the state of disease in active pulmonary TB patients. METHODS: We measured interferon (IFN)-gamma, tumor necrosis factor (TNF)-alpha and interleukin (IL)-10 levels in whole blood after stimulation with culture filtrate protein of Mycobacterium tuberculosis in 33 multi-drug resistant (MDR)-TB and 51 non-MDR-TB patients. RESULTS: No significant difference was found in IFN-gamma production between non-MDR-TB and MDR-TB patients, but there was a marked reduction in TNF-alpha production in MDR-TB patients accompanied by a moderate increase in IL-10 levels. In contrast, the presence of cavity was associated with a significant increase in IFN-gamma, whereas no difference in TNF-alpha between the cavity and non-cavity group was observed. Those who have TB lesions in the left lung showed lower levels of IFN-gamma and TNF-alpha and higher IL-10 levels than the patients with lesions on the right side. IFN-gamma levels were significantly increased in those with moderate or advanced lesions compared with patients with mild lesions. TNF-alpha and IL-10 levels did not change with disease severity. The number of M. tuberculosis bacilli in sputum was closely associated with TNF-alpha levels. The patient group with high value (+++) of sputum culture acid-fast bacilli produced significantly reduced levels of TNF-alpha compared with medium (++) and low (+) values. CONCLUSION: These findings suggest that IFN-gamma, TNF-alpha or IL-10 production patterns in whole blood are associated with disease progression in active pulmonary TB.-
dc.description.statementOfResponsibilityopen-
dc.format.extent331~337-
dc.relation.isPartOfRESPIRATION-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHDisease Progression*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHInterferon-gamma/blood-
dc.subject.MESHInterleukin-10/blood*-
dc.subject.MESHLung/diagnostic imaging-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRadiography-
dc.subject.MESHSeverity of Illness Index-
dc.subject.MESHSputum/microbiology-
dc.subject.MESHTuberculosis, Multidrug-Resistant/blood*-
dc.subject.MESHTuberculosis, Multidrug-Resistant/diagnostic imaging-
dc.subject.MESHTumor Necrosis Factor-alpha/blood*-
dc.titleTumor necrosis factor-alpha and interleukin-10 in whole blood is associated with disease progression in pulmonary multidrug-resistant tuberculosis patients-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Microbiology (미생물학)-
dc.contributor.googleauthorSeok-Yong Eum-
dc.contributor.googleauthorBo-Young Jeon-
dc.contributor.googleauthorJin-Hong Min-
dc.contributor.googleauthorSeung-Cheol Kim-
dc.contributor.googleauthorSungae Cho-
dc.contributor.googleauthorSeung-Kyu Park-
dc.contributor.googleauthorSang-Nae Cho-
dc.identifier.doi10.1159/000113932-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03824-
dc.relation.journalcodeJ02613-
dc.identifier.eissn1423-0356-
dc.identifier.pmid18212516-
dc.identifier.urlhttp://www.karger.com/Article/FullText/113932-
dc.subject.keywordPulmonary tuberculosis-
dc.subject.keywordMulti-drug resistance-
dc.subject.keywordCavity-
dc.subject.keywordAcid-fast bacilli-
dc.subject.keywordCytokines-
dc.contributor.alternativeNameCho, Sang Nae-
dc.contributor.affiliatedAuthorCho, Sang Nae-
dc.rights.accessRightsnot free-
dc.citation.volume76-
dc.citation.number3-
dc.citation.startPage331-
dc.citation.endPage337-
dc.identifier.bibliographicCitationRESPIRATION, Vol.76(3) : 331-337, 2008-
dc.identifier.rimsid56916-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers

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