Sm. Vanbeers et al., AN EPIDEMIOLOGIC-STUDY OF LEPROSY INFECTION BY SEROLOGY AND POLYMERASE CHAIN-REACTION, International journal of leprosy and other mycobacterial diseases, 62(1), 1994, pp. 1-9
A population-based study has been carried out in two adjacent villages
in a highly leprosy-endemic area of South Sulawesi, Indonesia; The pr
evalence of clinical leprosy was 10.0 per 1000 inhabitants. A total of
1015 serum samples and 1228 nasal swab specimens were collected. IgM
antibodies in blood to phenolic glycolipid-I (PGL-I) of Mycobacterium
leprae were demonstrated by the gelatin particle agglutination test (M
LPA) and by indirect ELISA (IgM-PGL). IgG antibodies to PGL-I (IgG-PGL
) and lipoarabinomannan-B (IgG-LAM) were measured by indirect ELISA. T
he presence of M. leprae in nasal swab specimens was established by a
polymerase chain reaction (PCR). The seropositivity rates in the popul
ation were 32% for MLPA, 30.8% for IgM-PGL, 6.7% for IgG-PGL, and 11.6
% for IgG-LAM. Seropositivity rates for MLPA and IgM-PGL were highest
in the younger age groups. There was no difference in seropositivity i
n any of the tests between household contacts of leprosy patients and
noncontacts. The seropositivity rates in the MLPA and IgM-PGL were not
randomly distributed among all households. The presence of M. leprae
by PCR was demonstrated in 7.8% of the nasal swab specimens. No correl
ation was found between the results of the PCR and serology. This stud
y indicates that M. leprae is widespread in the population, and that i
n endemic areas many individuals carry M. leprae in their nasal caviti
es without having obvious symptoms of leprosy.