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Novel strategies to identify biomarkers in tuberculosis

  • Marc Jacobsen , Jens Mattow , Dirk Repsilber und Stefan H.E. Kaufmann
Veröffentlicht/Copyright: 27. März 2008
Biological Chemistry
Aus der Zeitschrift Band 389 Heft 5

Abstract

The more we learn about the immune response against tuberculosis (TB) and particularly about the features which distinguish protective immunity, disease susceptibility and pathology, the better we can define biomarkers which correlate with these different stages of infection. The most widely used biomarker in TB, which without a doubt is an important component of protective immunity, is IFNγ secreted by antigen-specific CD4 T-cells. However, the complexity of the immune response against TB makes it more than likely that additional biomarkers are required for a reliable correlate of protection. As a corollary, we assume that a set of biomarkers will be required, termed a biosignature.


Corresponding author

Published Online: 2008-03-27
Published in Print: 2008-05-01

©2008 by Walter de Gruyter Berlin New York

Artikel in diesem Heft

  1. Guest Editorial
  2. Novel paradigms in vaccine development: from small pox eradication to therapeutic vaccines
  3. Highlight: 3rd Semmering Conference 2007
  4. Adaptive immune responses to hepatitis C virus: from viral immunobiology to a vaccine
  5. Dendritic cell subtypes as primary targets of vaccines: the emerging role and cross-talk of pattern recognition receptors
  6. Novel strategies to identify biomarkers in tuberculosis
  7. Not to wake a sleeping giant: new insights into host-pathogen interactions identify new targets for vaccination against latent Mycobacterium tuberculosis infection
  8. Lipopolysaccharide: a tool and target in enterobacterial vaccine development
  9. The coming of age of virus-like particle vaccines
  10. Maintenance of serological memory
  11. Adjuvant activity of type I interferons
  12. Japanese encephalitis vaccines – needs, flaws and achievements
  13. Analysis of the human cytomegalovirus pp65-directed T-cell response in healthy HLA-A2-positive individuals
  14. Non-regulatory CD8+CD45RO+CD25+ T-lymphocytes may compensate for the loss of antigen-inexperienced CD8+CD45RA+ T-cells in old age
  15. Pre-clinical development of cell culture (Vero)-derived H5N1 pandemic vaccines
  16. Construction of an encapsulated ESAT-6-based anti-TB DNA vaccine and evaluation of its immunogenic properties
  17. Review
  18. RNA switches regulate initiation of translation in bacteria
  19. Protein Structure and Function
  20. Inhibition of bacterial oxidases by formamide and analogs
  21. Modeling of variant copies of subunit D1 in the structure of photosystem II from Thermosynechococcus elongatus
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