Email updates

Keep up to date with the latest news and content from BMC Proceedings and BioMed Central.

This article is part of the supplement: Proceedings of Immunodiagnosis of Tuberculosis: New Questions, New Tools

Open Access Oral presentation

Host response to tuberculosis as basis for rational design of vaccines and biomarkers

Stefan HE Kaufmann

Author Affiliations

Department of Immunology, Max Planck Institute for Infection Biology, Berlin, 10117, Germany

BMC Proceedings 2010, 4(Suppl 3):O7  doi:10.1186/1753-6561-4-S3-O7


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/4/S3/O7


Published:17 December 2010

© 2010 Kaufmann; licensee BioMed Central Ltd.

Oral presentation

The current diagnostic techniques are not effective in key areas of tuberculosis (TB) research, such as predicting susceptibility, treatment outcome, and monitoring the effectiveness of drug or vaccine trials. Hence, more emphasis is to be placed on biomarker research. A biomarker is a characteristic feature that is objectively measured and evaluated as an indicator of a biological or pathological process or a response to therapy or prevention. Peripheral blood cells may not provide an accurate picture of what is happening in a TB patient at the site of disease manifestation, i.e., the granuloma. The fact that granulomas reach a point where they become largely autonomous and the immune response controls itself in the granuloma, has presented challenges. To address this point, our team infected splenectomized lymphotoxin β-receptor-deficient mice, which have no secondary lymphoid organs, with a small dose of Mycobacterium tuberculosis (M.tb). Without lymph nodes and spleen, the mice mounted an immune response and survived. Upon further analysis, CD8 and CD4 T-cells were generated in the granulomas as well as central memory and multifunctional T cells. Mice were then infected with M.tb, cured with antibiotics and then reinfected. When reinfected mice were compared to mice with a primary infection, we found that protective memory had developed. We conclude that granulomas can develop an immune response in the absence of lymph nodes and spleen. Moreover, in a study of TB lesions in humans, we found that the same appears to occur.

Using metabolomics, and working with the company Metabalon, we examined a combination of metabolites in latently infected individuals and patients with active TB disease to define a profile to differentiate healthy infected from diseased individuals. Diagnoses made by metabolomics profiles were equally accurate as clinical diagnoses. Metabolomics was also used to identify markers for cell exhaustion, which can lead to reinfection. In particular, we studied the metabolite tryptophan, the degradation of which is involved in suppressive mechanisms. These studies were complemented using transcriptomics. Dendritic cells were stimulated with ManLam, a bacterial cell wall lipid component that binds to DC-SIGN, a host cell receptor known to be involved in immunosupression. This binding also caused the cells to over-express the enzymes involved in the degradation of tryptophan. We consider this pathway to be involved in reactivation of TB and sustenance of active disease.