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1.
Cell Physiol Biochem ; 37(2): 409-18, 2015.
Article in English | MEDLINE | ID: mdl-26314826

ABSTRACT

Treatment for tuberculosis is effective with the use of proper antibiotics, but the number of drug-resistant cases is increasing. Drug resistance occurred in 650,000 cases of the 20 million patients in treatment worldwide in 2011, which demonstrates the necessity of finding new therapeutic approaches. In this context, the search for new medicines and immunomodulators could help reduce the prevalence and incidence of multi-drug-resistant tuberculosis cases. Thus several preclinical studies demonstrate the involvement of the P2X7 receptor (P2X7R) in the control of Mycobacterium tuberculosis (MTB) infection. Adenosine triphosphate (ATP), a natural agonist for P2X7R, promotes MTB death and the induction of apoptosis in monocytes and macrophages infected with MTB via activation of P2X7R by extracellular ATP. In addition, P2X7R activation in the presence of ATP increases the expression of major histocompatibility complex (MHC) class II by macrophages infected with Mycobacterium bovis (BCG) or MTB, which contributes to the generation of the antimicrobial immune response via T cells. Nevertheless, one idea that seems overlooked by the "purinergic community" is the use of the high-conductance channel associated with P2X7R to increase the passage of hydrophilic drugs to the cytoplasm of cells that express the P2X7 pore, a potential method for a drug delivery system. In this work, we propose the use of P2X7 agonists in conjunction with low molecular weight anti-tuberculosis medicines for the treatment of multi-drug-resistant tuberculosis.


Subject(s)
Adenosine Triphosphate/pharmacology , Receptors, Purinergic P2X7/metabolism , Tuberculosis/drug therapy , Adenosine Triphosphate/therapeutic use , Animals , Antitubercular Agents/therapeutic use , Drug Resistance, Bacterial , Drug Therapy, Combination , Gene Expression Regulation/drug effects , Humans , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/immunology , Receptors, Purinergic P2X7/genetics , Tuberculosis/genetics , Tuberculosis/metabolism
2.
Mem Inst Oswaldo Cruz ; 100(5): 459-65, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16184220

ABSTRACT

The vaccine Bacillus of Calmette Guérin (BCG) was originally developed in France as an oral vaccine against tuberculosis. The oral use of this vaccine was replaced by the parenteral route in almost all countries after the Lubeck disaster. In contrast, Brazil retained the oral delivery of the vaccine until the mid-seventies when it was replaced by the intradermal route. This change in route of delivery was mainly secondary to pressure by medical practitioners based on the poor responses of oral immunized subjects to purified protein derivative (PPD) skin tests. Even after the change of route of delivery, Ataulpho de Paiva Foundation continued making the oral vaccine. Currently, BCG Moreau has been described as one of the most immunogenic and with fewer side effects than other BCGs. The genomics, proteomics and vaccine trials for oral BCG Moreau Rio de Janeiro are currently under investigation. In this review, we intend to describe the history of BCG Moreau Rio de Janeiro in Brazil.


Subject(s)
BCG Vaccine/administration & dosage , Tuberculosis, Pulmonary/prevention & control , Vaccination/history , BCG Vaccine/history , Brazil , History, 19th Century , History, 20th Century , Tuberculosis, Pulmonary/history
3.
Mem. Inst. Oswaldo Cruz ; 100(5): 459-465, Aug. 2005. ilus
Article in English | LILACS | ID: lil-409960

ABSTRACT

The vaccine Bacillus of Calmette Guérin (BCG) was originally developed in France as an oral vaccine against tuberculosis. The oral use of this vaccine was replaced by the parenteral route in almost all countries after the Lubeck disaster. In contrast, Brazil retained the oral delivery of the vaccine until the mid-seventies when it was replaced by the intradermal route. This change in route of delivery was mainly secondary to pressure by medical practitioners based on the poor responses of oral immunized subjects to purified protein derivative (PPD) skin tests. Even after the change of route of delivery, Ataulpho de Paiva Foundation continued making the oral vaccine. Currently, BCG Moreau has been described as one of the most immunogenic and with fewer side effects than other BCGs. The genomics, proteomics and vaccine trials for oral BCG Moreau Rio de Janeiro are currently under investigation. In this review, we intend to describe the history of BCG Moreau Rio de Janeiro in Brazil.


Subject(s)
Humans , Infant, Newborn , Infant , History, 19th Century , History, 20th Century , BCG Vaccine/administration & dosage , Tuberculosis, Pulmonary/prevention & control , Vaccination/history , BCG Vaccine/history , Brazil , Tuberculosis, Pulmonary/history
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