M. K. Bhopale, H. Shah, Babu Lal Bamboria, A. Julka, I. Patel, V. K. Mahadik, M. Purohit
{"title":"Cytokine Responses in the Blood and Pleural Fluid of Pulmonary Tuberculosis Patients with and without HIV-1 Co-infection","authors":"M. K. Bhopale, H. Shah, Babu Lal Bamboria, A. Julka, I. Patel, V. K. Mahadik, M. Purohit","doi":"10.26502/JBB.2642-91280010","DOIUrl":null,"url":null,"abstract":"Tuberculosis (TB) is an opportunistic infectious disease with more severe forms in HIV-1 infected patients. The aim of the present study is to investigate the role of IFN-γ in the other cytokines belonging to Th1, Th17, Th22, and Th3 groups and CD4+ cell counts in the HIV-1 infection in patients co-infected with Mycobacterium tuberculosis. Clinically diagnosed patients of HIV-1, TB and HIV-1 co-infected with TB (HIV-1+TB) groups were selected to test IFN-γ IL-17, IL-22, TGF-β, and also CD4 counts in the blood for the study. Our results showed that IFN-γ and IL-17 cytokines were higher in HIV-1 and TB patients in serum when compared with healthy normal subjects, but there was an insignificant difference when compared with those in HIV-1+TB with TB patients’ samples. Pleural fluid samples of the HIV-1+TB patients showed significantly higher in IL-22 and IFN-γ cytokines than in TB patients, whereas IL-17 showed insignificant differences. CD4+ cells were counted in the blood of HIV-1, TB, and HIV-1+TB patients, however, the results showed that the counts were significantly lower than in the healthy normal group. There was a significantly lower CD4+ count in HIV-1+TB co-infected patients compared to TB patients, but not with HIV-1 patients. The present study suggests that IFN-γ and IL-17 play a significant role individually in HIV-1 and tuberculosis infected patients and IL-22 in pleural fluid in tuberculosis, which differs from those in HIV1 co-infected tuberculosis patients due to the severely affected immune system.","PeriodicalId":15066,"journal":{"name":"Journal of Biotechnology and Biomedicine","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biotechnology and Biomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26502/JBB.2642-91280010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Tuberculosis (TB) is an opportunistic infectious disease with more severe forms in HIV-1 infected patients. The aim of the present study is to investigate the role of IFN-γ in the other cytokines belonging to Th1, Th17, Th22, and Th3 groups and CD4+ cell counts in the HIV-1 infection in patients co-infected with Mycobacterium tuberculosis. Clinically diagnosed patients of HIV-1, TB and HIV-1 co-infected with TB (HIV-1+TB) groups were selected to test IFN-γ IL-17, IL-22, TGF-β, and also CD4 counts in the blood for the study. Our results showed that IFN-γ and IL-17 cytokines were higher in HIV-1 and TB patients in serum when compared with healthy normal subjects, but there was an insignificant difference when compared with those in HIV-1+TB with TB patients’ samples. Pleural fluid samples of the HIV-1+TB patients showed significantly higher in IL-22 and IFN-γ cytokines than in TB patients, whereas IL-17 showed insignificant differences. CD4+ cells were counted in the blood of HIV-1, TB, and HIV-1+TB patients, however, the results showed that the counts were significantly lower than in the healthy normal group. There was a significantly lower CD4+ count in HIV-1+TB co-infected patients compared to TB patients, but not with HIV-1 patients. The present study suggests that IFN-γ and IL-17 play a significant role individually in HIV-1 and tuberculosis infected patients and IL-22 in pleural fluid in tuberculosis, which differs from those in HIV1 co-infected tuberculosis patients due to the severely affected immune system.