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   Host Immune Responses Differ between M. africanum- and M. tuberculosis-Infected Patients following Standard Anti-tuberculosis Treatment  
   
نویسنده tientcheu l.d. ,haks m.c. ,agbla s.c. ,sutherland j.s. ,adetifa i.m. ,donkor s. ,quinten e. ,daramy m. ,antonio m. ,kampmann b. ,ottenhoff t.h.m. ,dockrell h.m. ,ota m.o.
منبع plos neglected tropical diseases - 2016 - دوره : 10 - شماره : 5
چکیده    Epidemiological differences exist between mycobacterium africanum (maf)- and mycobacterium tuberculosis (mtb)-infected patients,but to date,contributing host factors have not been characterised. we analysed clinical outcomes,as well as soluble markers and gene expression profiles in unstimulated,and esat6/cfp-10-,whole-maf- and mtb-stimulated blood samples of 26 maf- and 49 mtb-hiv-negative tuberculosis patients before,and after 2 and 6 months of anti-tuberculosis therapy. before treatment,both groups had similar clinical parameters,but differed in few cytokines concentration and gene expression profiles. following treatment the body mass index,skinfold thickness and chest x-ray scores showed greater improvement in the mtb- compared to maf-infected patients,after adjusting for age,sex and ethnicity (p = 0.02; 0.04 and 0.007,respectively). in addition,in unstimulated blood,il-12p70,il12a and tlr9 were significantly higher in maf-infected patients,while il-15,il-8 and mip-1α were higher in mtb-infected patients. overnight stimulation with esat-6/cfp-10 induced significantly higher levels of ifn-γ and tnf-α production,as well as gene expression of ccl4,il1b and tlr4 in mtb- compared to maf-infected patients. our study confirms differences in clinical features and immune genes expression and concentration of proteins associated with inflammatory processes between mtb- and maf-infected patients following anti-tuberculosis treatment these findings have public health implications for treatment regimens,and biomarkers for tuberculosis diagnosis and susceptibility. © 2016 tientcheu et al.
آدرس vaccines and immunity theme,medical research council unit,banjul,gambia,department of immunology and infection,faculty of infectious and tropical diseases,london school of hygiene and tropical medicine,london,united kingdom,department of biochemistry,faculty of science,university of yaoundé 1,yaoundé, Cameroon, department of infectious diseases,leiden university medical center,leiden, Netherlands, vaccines and immunity theme,medical research council unit,banjul,gambia,department of medical statistics,faculty of epidemiology and population health,london school of hygiene and tropical medicine,london, United Kingdom, vaccines and immunity theme,medical research council unit,banjul, Gambia, disease control and elimination theme,medical research council unit,fajara,gambia,department of infectious diseases epidemiology,faculty of epidemiology and population health,london school of hygiene and tropical medicine,london, United Kingdom, vaccines and immunity theme,medical research council unit,banjul, Gambia, department of infectious diseases,leiden university medical center,leiden, Netherlands, vaccines and immunity theme,medical research council unit,banjul, Gambia, vaccines and immunity theme,medical research council unit,banjul,gambia,department of pathogen molecular biology,faculty of infectious and tropical diseases,london school of hygiene & tropical medicine,london,united kingdom,microbiology and infection unit,warwick medical school,university of warwick,coventry, United Kingdom, vaccines and immunity theme,medical research council unit,banjul, Gambia, department of infectious diseases,leiden university medical center,leiden, Netherlands, department of immunology and infection,faculty of infectious and tropical diseases,london school of hygiene and tropical medicine,london, United Kingdom, vaccines and immunity theme,medical research council unit,banjul,gambia,world health organization regional office for africa,brazzaville, Congo
 
     
   
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