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Variation in Gamma Interferon Responses to Different Infecting Strains of Mycobacterium tuberculosisin Acid-Fast Bacillus Smear-Positive Patients and Household Contacts in Antananarivo, Madagascar
- Source :
- Clinical and Vaccine Immunology (formerly CDLI); July 2010, Vol. 17 Issue: 7 p1094-1103, 10p
- Publication Year :
- 2010
-
Abstract
- ABSTRACTThe majority of healthy individuals exposed to Mycobacterium tuberculosiswill not develop tuberculosis (TB), though many may become latently infected. More precise measurement of the human immune response to M. tuberculosisinfection may help us understand this difference and potentially identify those subjects most at risk of developing active disease. Gamma interferon (IFN-?) production has been widely used as a proxy marker to study infection and to examine the human immune response to specific M. tuberculosisantigens. It has been suggested that genetically distinct M. tuberculosisstrains may invoke different immune responses, although how these differences influence the immune responses and clinical outcome in human tuberculosis is still poorly understood. We therefore evaluated the antigen-specific IFN-? production responses in peripheral blood mononuclear cells from two cohorts of subjects recruited in Antananarivo, Madagascar, from 2004 to 2006 and examined the influence of the infecting M. tuberculosisstrains on this response. The cohorts were sputum-positive index cases and their household contacts. Clinical strains isolated from the TB patients were typed by spoligotyping. Comparison of the IFN-? responses with the spoligotype of the infecting clinical strains showed that “modern” M. tuberculosisstrains, like Beijing and Central Asian (CAS) strains, tended to induce lower IFN-? responses than “ancient” strains, like East African-Indian (EAI) strains, in index cases and their household contacts. These results suggest that new strains may have evolved to induce a host response different from that of ancient strains. These findings could have important implications in the development of therapeutic and diagnostic strategies.
Details
- Language :
- English
- ISSN :
- 15566811 and 1556679X
- Volume :
- 17
- Issue :
- 7
- Database :
- Supplemental Index
- Journal :
- Clinical and Vaccine Immunology (formerly CDLI)
- Publication Type :
- Periodical
- Accession number :
- ejs57510734
- Full Text :
- https://doi.org/10.1128/CVI.00049-10