Detection of the 70-kilodalton Histoplasma capsulatum antigen in serum of histoplasmosis patients: Correlation between antigenemia and therapy duringfollow-up
Bl. Gomez et al., Detection of the 70-kilodalton Histoplasma capsulatum antigen in serum of histoplasmosis patients: Correlation between antigenemia and therapy duringfollow-up, J CLIN MICR, 37(3), 1999, pp. 675-680
Histoplasmosis is an important systemic fungal infection, particularly amon
g immunocompromised individuals, who may develop a progressive disseminated
form which is often fatal if it is untreated. In such patients, the detect
ion of antibody responses for both diagnosis and follow-up may be of limite
d use, whereas the detection of Histoplasma capsulatum var, capsulatum anti
gens may provide a more practical approach. We have recently described an i
nhibition enzyme-linked immunosorbent assay (ELISA) for the detection in pa
tients' sera of a 69- to 70-kDa H. capsulatum var, capsulatum-specific anti
gen which appears to be useful in diagnosis. To investigate its potential f
or the follow-up of histoplasmosis patients during treatment, antigen titer
s in the sera of 16 patients presenting with different clinical forms of hi
stoplasmosis were monitored at regular intervals for up to 80 weeks. Sera f
rom four of five patients with the acute form of the disease showed rapid f
alls in antigenemia, becoming antigen negative by week 14 (range, weeks 10
to 16). Sera from four patients with disseminated histoplasmosis showed fal
ls in antigen levels; three of them became antigen negative by week 32; the
fourth patient became negative by week 48. In contrast, antigen titers in
four of six AIDS patients with the disseminated form of the disease remaine
d positive throughout follow-up. Sera from only one patient who presented w
ith the chronic form of the disease were analyzed, and this individual's se
rum became antigen negative by week 9. The inhibition ELISA is shown to be
of particular use in the monitoring of non-AIDS patients with the acute and
disseminated forms of the disease and may complement existing means of fol
low-up.