02648nas a2200433 4500000000100000008004100001260001300042653001000055653002500065653001100090653001900101653001100120653002500131653002500156653002100181653001600202653000900218653001600227653002100243653002500264653001600289100001800305700002400323700001600347700001500363700001400378700002200392700002400414700002100438700001700459700001700476245008300493856005100576300001200627490000700639050001800646520153600664022001402200 2011 d c2011 Dec10aAdult10aCase-Control Studies10aFemale10aFlow Cytometry10aHumans10aLeprosy, lepromatous10aLeprosy, Tuberculoid10aLymphocyte Count10aLymphocytes10aMale10aMiddle Aged10aReceptors, CXCR410aReceptors, Chemokine10aYoung Adult1 aMendonça V A1 aAlvim de Melo G E B1 aAraújo M G1 aBorges V O1 aCosta R D1 aMartins-Filho O A1 aTeixeira-Carvalho A1 aSathler-Avelar R1 aTeixeira M M1 aTeixeira A L00aExpression of the chemokine receptor CXCR4 on lymphocytes of leprosy patients. uhttp://www.scielo.br/pdf/bjmbr/v44n12/1193.pdf a1256-600 v44 aMENDONҪA20113 a

Leprosy is caused by Mycobacterium leprae, which induces chronic granulomatous infection of the skin and peripheral nerves. The disease ranges from the tuberculoid to the lepromatous forms, depending on the cellular immune response of the host. Chemokines are thought to be involved in the immunopathogenesis of leprosy, but few studies have investigated the expression of chemokine receptors on leukocytes of leprosy patients. In the present study, we evaluated 21 leprosy patients (M/F: 16/5) with a new diagnosis from the Dermatology Outpatient Clinic of the University Hospital, Federal University of Minas Gerais. The control group was composed of 20 healthy members (M/F: 15/5) of the community recruited by means of announcements. The expression of CCR2, CCR3, CCR5, and CXCR4 was investigated by flow cytometry on the surface of peripheral blood lymphocytes. There was a decrease in percentage of CD3+CXCR4+ and CD4+CXCR4+ lymphocytes in the peripheral blood of leprosy patients (median [range], 17.6 [2.7-41.9] and 65.3 [3.9-91.9], respectively) compared to the control group (median [range], 43.0 [3.7-61.3] and 77.2 [43.6-93.5], respectively). The percentage of CD4+CXCR4+ was significantly lower in patients with the tuberculoid form (median [range], 45.7 [0.0-83.1]) of the disease, but not in lepromatous patients (median [range], 81.5 [44.9-91.9]). The CXCR4 chemokine receptor may play a role in leprosy immunopathogenesis, probably directing cell migration to tissue lesions in tuberculoid leprosy patients.

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