|
|
Peptides derived from mycobacterium leprae ML1601c discriminate between leprosy patients and healthy endemic controls
|
|
|
|
|
نویسنده
|
bobosha k. ,van der ploeg-van schip j.j. ,esquenazi d.a. ,guimarães m.m. ,martins m.v. ,bekele y. ,fantahun y. ,aseffa a. ,franken k.l.m.c. ,gismondi r.c. ,pessolani m.c.v. ,ottenhoff t.h.m. ,pereira g.m.b. ,geluk a.
|
منبع
|
journal of tropical medicine - 2012 - شماره : 0
|
چکیده
|
The stable incidence of new leprosy cases suggests that transmission of infection continues despite worldwide implementation of mdt. thus,specific tools are needed to diagnose early stage mycobacterium leprae infection,the likely sources of transmission. m. leprae antigens that induce t-cell responses in m. leprae exposed and/or infected individuals thus are major targets for new diagnostic tools. previously,we showed that ml1601c was immunogenic in patients and healthy household contacts (hhc). however,some endemic controls (ec) also recognized this protein. to improve the diagnostic potential,ifn-γ responses to ml1601c peptides were assessed using pbmc from brazilian leprosy patients and ec. five ml1601c peptides only induced ifn-γ in patients and hhc. moreover,24-hour whole-blood assay (wba),two ml1601c peptides could assess the level of m. leprae exposure in ethiopian ec. beside ifn-γ,also ip-10,il-6,il-1β,tnf-α,and mcp-1 were increased in ec from areas with high leprosy prevalence in response to these ml1601c peptides. thus,ml1601c peptides may be useful for differentiating m. leprae exposed or infected individuals and can also be used to indicate the magnitude of m. leprae transmission even in the context of various hla alleles as present in these different genetic backgrounds. copyright 2012 kidist bobosha et al.
|
|
|
آدرس
|
department of infectious diseases,lumc,p.o. box 9600,2300 rc leiden,netherlands,leprosy section,armauer hansen research institute,p.o. box 1005, Ethiopia, department of infectious diseases,lumc,p.o. box 9600, Netherlands, laboratory of cellular microbiology,oswaldo cruz institute,fiocruz,21040-360 rio de janeiro,rj,brazil,school of medical sciences,state university of rio de janeiro,20550-170 rio de janeiro, Brazil, laboratory of cellular microbiology,oswaldo cruz institute,fiocruz,21040-360 rio de janeiro, Brazil, laboratory of cellular microbiology,oswaldo cruz institute,fiocruz,21040-360 rio de janeiro, Brazil, leprosy section,armauer hansen research institute,p.o. box 1005, Ethiopia, leprosy section,armauer hansen research institute,p.o. box 1005, Ethiopia, leprosy section,armauer hansen research institute,p.o. box 1005, Ethiopia, department of infectious diseases,lumc,p.o. box 9600, Netherlands, school of medical sciences,state university of rio de janeiro,20550-170 rio de janeiro, Brazil, laboratory of cellular microbiology,oswaldo cruz institute,fiocruz,21040-360 rio de janeiro, Brazil, department of infectious diseases,lumc,p.o. box 9600, Netherlands, laboratory of cellular microbiology,oswaldo cruz institute,fiocruz,21040-360 rio de janeiro,rj,brazil,school of medical sciences,state university of rio de janeiro,20550-170 rio de janeiro, Brazil, department of infectious diseases,lumc,p.o. box 9600, Netherlands
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Authors
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|