Tuberculosis and multi-drug resistant tuberculosis: immunologic mechanisms and tools for controlling the disease
DOI:
https://doi.org/10.3395/reciis.v2i1.831Keywords:
Tuberculosis, multi-drug resistant, diagnosis, IFN-y, immunologic mechanismsAbstract
It is estimated that one third of the world’s population is infected with Mycobacterium tuberculosis. In 2005, the World Health Organization estimated that eight million people died from tuberculosis worldwide. The official indicators point to a decline in tuberculosis rates in the past century but since 1990 the incidence rates are increasing again. Despite the existence of medicines effective in the control of tuberculosis, the cases of multi-drug resistance have increased worldwide. Recently the problem became even worse with the emergence of strains extremely resistant to drugs, responsible for what the WHO calls XDRTB (extensively drug resistant tuberculosis). The only vaccine available against this disease, the BCG vaccine, is efficient in preventing severe forms of tuberculosis in children. Its efficiency in adults however varies considerably and it has been demonstrated that revaccination does not increase the degree of protection in adolescents and adults. Various studies demonstrated that, in the attempt to contain the infection, the host cells develop immunoregulatory and mycobactericide mechanisms, and that failures in these mechanisms allow the disease to advance. The aim of this article is to review the data related to the immune response in patients with tuberculosis and multi-drug resistant tuberculosis (MDR-TB) and to show how these findings can contribute to the development of new diagnostic strategies and/or vaccines to control the disease.Downloads
Published
How to Cite
Issue
Section
License
Author’s rights: The author retains unrestricted rights over his work.
Rights to reuse: Reciis adopts the Creative Commons License, CC BY-NC non-commercial attribution according to the Policy on Open Access to Knowledge by Oswaldo Cruz Foundation. With this license, access, download, copy, print, share, reuse, and distribution of articles is allowed, provided that it is for non-commercial use and with source citation, granting proper authorship credits and reference to Reciis. In such cases, no permission is required from the authors or editors.
Rights of authors’s deposit / self-archiving: The authors are encouraged to deposit the published version, along with the link of their article in Reciis, in institutional repositories.