TY - JOUR KW - Adult KW - Aged KW - Chemokine CCL11 KW - Chemokine CCL24 KW - Chemokines KW - Clofazimine KW - Dapsone KW - Drug Therapy, Combination KW - Female KW - Humans KW - Laboratories KW - Leprostatic Agents KW - leprosy KW - Male KW - Middle Aged KW - Mycobacterium leprae KW - Rifampin KW - Treatment Outcome AU - Mendonça VA AU - Costa RD AU - Lyon S AU - Penido RA AU - Borges VO AU - Bretas TL AU - Antunes CM AU - Teixeira MM AU - Teixeira AL AB -

Leprosy, whose etiologic agent is Mycobacterium leprae, is an illness of ample clinical and immunopathological spectrum. Although chemokines seem to be involved in the immunopathogenesis of leprosis, few studies have been carried out to unveil the potential of chemokines as biological markers of the disease. The purpose of this study was to investigate the value of measuring CCL2, CCL3, CCL11 and CCL24 in plasma of patients with leprosy (LE) at different stages of multi-drug therapy (MDT). Chemokines were measured by ELISA in plasma of 30 non-infected individuals (NI) and 33 LE patients before and at different stages of treatment. The plasma concentration of CCL11 (p<0.01) and CCL24 (p<0.05) was increased in LE patients before treatment when compared to NI individuals. The plasma concentration of CCL24 decreased after MDT (p<0.05). No differences were observed in the concentration of CCL2 and CCL3 in plasma of NI and LE individuals. The elevated levels of CCL11 and CCL24 in plasma of patients with LE suggest that these chemokines may play a role in disease pathogenesis. Moreover, the decrease of CCL24 after treatment suggests that this chemokine might be useful as a biomarker of response to MDT in patients with leprosy.

BT - Acta tropica C1 - http://www.ncbi.nlm.nih.gov/pubmed/19874796?dopt=Abstract DA - 2010 Feb DO - 10.1016/j.actatropica.2009.10.010 IS - 2 J2 - Acta Trop. LA - eng N2 -

Leprosy, whose etiologic agent is Mycobacterium leprae, is an illness of ample clinical and immunopathological spectrum. Although chemokines seem to be involved in the immunopathogenesis of leprosis, few studies have been carried out to unveil the potential of chemokines as biological markers of the disease. The purpose of this study was to investigate the value of measuring CCL2, CCL3, CCL11 and CCL24 in plasma of patients with leprosy (LE) at different stages of multi-drug therapy (MDT). Chemokines were measured by ELISA in plasma of 30 non-infected individuals (NI) and 33 LE patients before and at different stages of treatment. The plasma concentration of CCL11 (p<0.01) and CCL24 (p<0.05) was increased in LE patients before treatment when compared to NI individuals. The plasma concentration of CCL24 decreased after MDT (p<0.05). No differences were observed in the concentration of CCL2 and CCL3 in plasma of NI and LE individuals. The elevated levels of CCL11 and CCL24 in plasma of patients with LE suggest that these chemokines may play a role in disease pathogenesis. Moreover, the decrease of CCL24 after treatment suggests that this chemokine might be useful as a biomarker of response to MDT in patients with leprosy.

PY - 2010 SP - 151 EP - 4 T2 - Acta tropica TI - Plasma levels of chemokines during leprosy specific treatment. VL - 113 SN - 1873-6254 ER -