EVALUATION OF PARACOCCIDIOIDES-BRASILIENSIS EXOANTIGEN IN THE DETECTION OF DELAYED DERMAL HYPERSENSITIVITY IN EXPERIMENTAL AND HUMAN PARACOCCIDIOIDOMYCOSIS
M. Marques et al., EVALUATION OF PARACOCCIDIOIDES-BRASILIENSIS EXOANTIGEN IN THE DETECTION OF DELAYED DERMAL HYPERSENSITIVITY IN EXPERIMENTAL AND HUMAN PARACOCCIDIOIDOMYCOSIS, Journal of medical and veterinary mycology, 34(4), 1996, pp. 265-272
The exoantigen of Paracoccidioides brasiliensis standardized by Camarg
o et al. [1] (AgR) was used to evaluate the in vivo and in vitro cell
immune response of experimental animals and of patients with paracocci
dioidomycosis (PBM). Fava Netto antigen (AgF) was tested in parallel a
s a control antigen. The study was conducted with mice and guinea pigs
infected with P. brasiliensis or immunized with its fungal antigens,
on patients with PBM and on their respective control groups. The cell
immune response was analysed by skin tests, and by the macrophage and
leucocyte migration inhibition tests (MMIT and LMIT) in the animals an
d in the patients, respectively. The skin test with AgR as paracoccidi
oidin was positive in infected or immunized mice and guinea pigs and n
egative in control animals. The skin tests with AgR (24 h) showed 96.7
% positivity in patients with PBM and were negative in control individ
uals. Histopathological study of the in vivo tests in the different ex
perimental models was consistent with a delayed hypersensitivity respo
nse (DHR). Immunohistochemical study of the skin tests of PBM patients
demonstrated a predominance of T lymphocytes, confirming the nature o
f a DHR to the fungal antigens. The in vitro cell immune response show
ed variable results for the various experimental models, i.e. signific
ant rates of MMIT in immunized mice, a tendency to positivity in infec
ted guinea pigs, and the absence of migration inhibition in PBM patien
ts. Taken together, the data indicate that the AgR is efficient as par
acoccidioidin in the evaluation of DHR in PBM, with an optimum time of
reading the test of 24 h.