@article{25026, keywords = {Brazil; Diagnosis; Leprosy; Mycobacterium leprae; Serology}, author = {Souza MM and Netto EM and Nakatani M and Duthie M}, title = {Utility of recombinant proteins LID-1 and PADL in screening for Mycobacterium leprae infection and leprosy.}, abstract = {

BACKGROUND: Despite the widespread use of multidrug therapy, leprosy remains an important public health concern in many regions. Detection is generally limited to clinical exam.

METHODS: As a two-tiered active case finding strategy, we used the LID-1 (leprosy IDRI diagnostic-1), and PADL (protein advances for the diagnosis of leprosy) antigens for serological examination of 2526 individuals randomly selected from 10 472 residents in a leprosy hyperendemic area (Cajazeiras, Paraiba, Brazil). Almost all seropositive (95%) and a subset of seronegative (17%) subjects then underwent clinical evaluations.

RESULTS: Prevalence of clinically apparent leprosy was 2.3% (19 cases among 834 fully examined individuals). LID-1 and PADL demonstrated a high sensitivity for supporting leprosy diagnosis at 89% and 87%, with positive predictive values (PPV) of 3.5% and 3.7%. The specificity for clinically apparent leprosy was low at 42% and 38%, respectively, and was likely reduced due to the presence of many asymptomatic individuals infected with Mycobacterium leprae.

CONCLUSIONS: Our data indicate the utility of the LID-1 and PADL antigens as primary screening tools for the detection of M. leprae infection and identification of leprosy patients. The follow-up of seropositive subjects could clarify the predictive value and utility of detecting anti-LID-1 and PADL antibodies within leprosy control programs.

}, year = {2014}, journal = {Transactions of the Royal Society of Tropical Medicine & Hygiene}, volume = {108}, pages = {495-501}, issn = {1878-3503}, doi = {10.1093/trstmh/tru093}, language = {eng}, }