02863nas a2200409 4500000000100000008004100001260001300042653001200055653001500067653002000082653001700102653001100119653002900130653001200159653002400171653001300195653002100208653001500229653002400244653000900268653001100277653003000288653002200318100001400340700001500354700001600369700001600385700001400401700001700415245016000432856005100592300001000643490000700653050003200660520174700692022001402439 2006 d c2006 Jun10aAnimals10aAntibodies10aChronic Disease10aCyclosporine10aHumans10aImmunosuppressive Agents10aleprosy10aNerve Growth Factor10aNeuritis10aPain Measurement10aPC12 Cells10aProspective Studies10aRats10aReflex10aSeverity of Illness Index10aTreatment Outcome1 aSena CBCD1 aSalgado CG1 aTavares CMP1 aDa Cruz CAV1 aXavier MB1 aNascimento J00aCyclosporine A treatment of leprosy patients with chronic neuritis is associated with pain control and reduction in antibodies against nerve growth factor. uhttps://leprosyreview.org/article/77/2/12-1129 a121-90 v77 aInfolep Library - available3 a
OBJECTIVES: Chronic neuritis (CN) is still a major problem in leprosy and is difficult to manage in patients who do not respond well to prednisone. In this study we (i) evaluate the efficacy of cyclosporine A (CyA) in controlling CN patients, and (ii) analyse the presence of anti-NGF antibodies in the sera of leprosy patients, and their behaviour during CyA treatment.
DESIGN: This was an open, prospective, non-comparative study. Sixty-seven leprosy patients in three different institutions in ParĂ¡, Brazil were studied from January, 2001 to January, 2004. Of these, 47 had no CN and 20 were leprosy patients suffering from CN and taking at least 40 mg/day prednisone to control nerve impairment and pain. Patients received 12 months reducing course CyA starting at 5 mg/kg per day. The outcome measure was sensory impairment, assessed using Semmes-Weinstein monofilament examination (SWME), muscular force and spontaneous or palpation-related pain.
RESULTS: Antibodies against NGF were detected in the sera of leprosy patients, which may explain the depletion of NGF in leprosy contributing to neuritis, inflammation and loss of cutaneous nociception. The levels of these antibodies in CN patients were slightly lower than in patients with no CN. However, anti-NGF titres in CN patients treated with CyA were lowered to levels similar to those in the normal subjects. There was also improvement in sensory impairment, muscular force and pain.
CONCLUSIONS: These data suggest that anti-NGF antibodies are present in the sera of leprosy patients and may influence the outcome of neuritis, and that CyA might be a useful drug in controlling nerve impairment and pain in leprosy patients.
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