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Recombinant Leishmania Antigens for Serodiagnosis of Visceral Leishmaniasis
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ABSTRACT
Serological tests with crude or recombinant
Leishmania
antigens are important tools for the diagnosis of leishmania infection. However, these tests are not markers of active visceral leishmaniasis (VL), since antibodies to these markers are often observed in individuals with subclinical
L. chagasi
infection and they do not fall shortly after therapy. In this study, levels of immunoglobulin G (IgG) against three recombinant
Leishmania
antigens (rH2A, KMP11, and the “Q” protein) were evaluated in sera from individuals with subclinical
L. chagasi
infection and in patients with VL pre- and posttherapy. The sensitivity of the serological test for diagnosis of VL was 100% with all three antigens. The titers of IgG fell significantly after therapy. While most of the individuals with subclinical
L. chagasi
infection had antibodies to rH2A and the “Q” protein, only 1 out of 15 individuals had antibodies to KMP11. These data indicate that KMP11 may be used to discriminate
L. chagasi
infection from active VL and may serve as a marker of response to therapy.
American Society for Microbiology
Title: Recombinant
Leishmania
Antigens for Serodiagnosis of Visceral Leishmaniasis
Description:
ABSTRACT
Serological tests with crude or recombinant
Leishmania
antigens are important tools for the diagnosis of leishmania infection.
However, these tests are not markers of active visceral leishmaniasis (VL), since antibodies to these markers are often observed in individuals with subclinical
L.
chagasi
infection and they do not fall shortly after therapy.
In this study, levels of immunoglobulin G (IgG) against three recombinant
Leishmania
antigens (rH2A, KMP11, and the “Q” protein) were evaluated in sera from individuals with subclinical
L.
chagasi
infection and in patients with VL pre- and posttherapy.
The sensitivity of the serological test for diagnosis of VL was 100% with all three antigens.
The titers of IgG fell significantly after therapy.
While most of the individuals with subclinical
L.
chagasi
infection had antibodies to rH2A and the “Q” protein, only 1 out of 15 individuals had antibodies to KMP11.
These data indicate that KMP11 may be used to discriminate
L.
chagasi
infection from active VL and may serve as a marker of response to therapy.
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