Rajiv Hira, Vishwas Sarangdhar, S. Hira, H. Dupont
{"title":"在印度孟买检测艾滋病毒/艾滋病患者外周血结核分枝杆菌的PCR","authors":"Rajiv Hira, Vishwas Sarangdhar, S. Hira, H. Dupont","doi":"10.5580/1396","DOIUrl":null,"url":null,"abstract":"Background: Since the co-infection of Mycobacterium tuberculosis (MTB) and HIV is recognized as a lethal combination, there is need for a reliable diagnostic test that can be conducted on a readily available specimen such as peripheral blood to periodically screen HIV-infected individuals for MTB at an early stage. Methods: A study was designed to assess the diagnostic value of PCR targeted to IS 1081 in peripheral blood of HIV-infected individuals because of ease of obtaining periodic samples. A cohort of 129 individuals was recruited for this purpose. It contained of adult, non-pregnant HIV sero-positive as well as HIV sero-negative individuals who were naïve to anti-Koch’s treatment at two teaching hospitals in Mumbai. Results: The cohort of 129 individuals was categorized into 5 groups based on their clinical TB and HIV status. The mean CD4 count for TB+HIV+(Groups 1,2,3) ranged between 381 and 525 cells/cmm suggesting early to moderate immune suppression.TB PCR assay was compared with the ‘gold’ standard, namely the LJ culture in each of the 5 groups. Overall, the sensitivity of PCR was 83.3% and specificity was 97.1%. PCR+ LJ-were subjected to sequential TB PCR tests at intervals of two weeks after initiation of AKT.TB PCR+ patients converted to TB PCR negative between 6-8 weeks. Conclusions: The study established that PCR targeted to IS 1081 is a valuable test for early diagnosis of TB from peripheral blood at an early point of TB activation when most patients (>85%) did not produce other traditional specimens such as the sputum and/or pleural fluid.","PeriodicalId":22514,"journal":{"name":"The Internet journal of microbiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2009-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Peripheral blood PCR for detection of Mycobacterium tuberculosis in patients with Hiv/Aids In Mumbai, India\",\"authors\":\"Rajiv Hira, Vishwas Sarangdhar, S. Hira, H. Dupont\",\"doi\":\"10.5580/1396\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Since the co-infection of Mycobacterium tuberculosis (MTB) and HIV is recognized as a lethal combination, there is need for a reliable diagnostic test that can be conducted on a readily available specimen such as peripheral blood to periodically screen HIV-infected individuals for MTB at an early stage. Methods: A study was designed to assess the diagnostic value of PCR targeted to IS 1081 in peripheral blood of HIV-infected individuals because of ease of obtaining periodic samples. A cohort of 129 individuals was recruited for this purpose. It contained of adult, non-pregnant HIV sero-positive as well as HIV sero-negative individuals who were naïve to anti-Koch’s treatment at two teaching hospitals in Mumbai. Results: The cohort of 129 individuals was categorized into 5 groups based on their clinical TB and HIV status. The mean CD4 count for TB+HIV+(Groups 1,2,3) ranged between 381 and 525 cells/cmm suggesting early to moderate immune suppression.TB PCR assay was compared with the ‘gold’ standard, namely the LJ culture in each of the 5 groups. Overall, the sensitivity of PCR was 83.3% and specificity was 97.1%. PCR+ LJ-were subjected to sequential TB PCR tests at intervals of two weeks after initiation of AKT.TB PCR+ patients converted to TB PCR negative between 6-8 weeks. Conclusions: The study established that PCR targeted to IS 1081 is a valuable test for early diagnosis of TB from peripheral blood at an early point of TB activation when most patients (>85%) did not produce other traditional specimens such as the sputum and/or pleural fluid.\",\"PeriodicalId\":22514,\"journal\":{\"name\":\"The Internet journal of microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Internet journal of microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5580/1396\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Internet journal of microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5580/1396","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Peripheral blood PCR for detection of Mycobacterium tuberculosis in patients with Hiv/Aids In Mumbai, India
Background: Since the co-infection of Mycobacterium tuberculosis (MTB) and HIV is recognized as a lethal combination, there is need for a reliable diagnostic test that can be conducted on a readily available specimen such as peripheral blood to periodically screen HIV-infected individuals for MTB at an early stage. Methods: A study was designed to assess the diagnostic value of PCR targeted to IS 1081 in peripheral blood of HIV-infected individuals because of ease of obtaining periodic samples. A cohort of 129 individuals was recruited for this purpose. It contained of adult, non-pregnant HIV sero-positive as well as HIV sero-negative individuals who were naïve to anti-Koch’s treatment at two teaching hospitals in Mumbai. Results: The cohort of 129 individuals was categorized into 5 groups based on their clinical TB and HIV status. The mean CD4 count for TB+HIV+(Groups 1,2,3) ranged between 381 and 525 cells/cmm suggesting early to moderate immune suppression.TB PCR assay was compared with the ‘gold’ standard, namely the LJ culture in each of the 5 groups. Overall, the sensitivity of PCR was 83.3% and specificity was 97.1%. PCR+ LJ-were subjected to sequential TB PCR tests at intervals of two weeks after initiation of AKT.TB PCR+ patients converted to TB PCR negative between 6-8 weeks. Conclusions: The study established that PCR targeted to IS 1081 is a valuable test for early diagnosis of TB from peripheral blood at an early point of TB activation when most patients (>85%) did not produce other traditional specimens such as the sputum and/or pleural fluid.