R. Malik et al., A LATEX CRYPTOCOCCAL ANTIGEN AGGLUTINATION-TEST FOR DIAGNOSIS AND MONITORING OF THERAPY FOR CRYPTOCOCCOSIS, Australian Veterinary Journal, 74(5), 1996, pp. 358-364
A latex cryptococcal antigen agglutination test (LCAT) was performed o
n sera obtained during the first 14 days of treatment from 58 animals
(46 cats, 9 dogs, 2 koalas and 1 long billed corella) with cryptococco
sis. The same commercial kit was used for all samples, and most serum
samples were treated with pronase before testing. Sera from all 58 cas
es tested positive with the qualitative LCAT protocol (using undiluted
sera), while sera from all 26 cats without cryptococcosis rested nega
tive. Titres determined using the quantitative protocol ranged from 1
to greater than or equal to 131 072 (median titre between 2048 and 409
6), with 57 of 58 cases (including all 8 animals that presented for ne
urological signs) having tires greater than or equal to 2 and thus con
sidered positive according to the manufacturer's recommendations. The
LCAT titre was positively correlated with disease severity (r = 0.4169
; P = 0.0011), and patients with disseminated skin and/or lymph node i
nvolvement had significantly higher titres than those that did not (P
= 0.0157). The presence of neurological signs, the species of the pati
ent, concurrent viral disease (in cats) and the biotype of the isolate
had no significant association with the LCAT titre, Cats that died of
active cryptococcosis despite treatment did not have significantly hi
gher titres (P = 0.3010) than those that responded to treatment. Seque
ntial LCAT determinations obtained in 37 patients during treatment pro
vided a useful quantitative indication of clinical progress, although
the decline in titre lagged somewhat behind clinical improvement, Gene
rally, the antigen titre declined by 2 to 4 fold per month during succ
essful therapy. Although there are insufficent data to make unequivoca
l recommendations, we suggest that either antifungal therapy be contin
ued until the LCAT titre declines to less than 1, or therapy be discon
tinued after a 32 fold or greater reduction in titre, with periodic mo
nitoring of the serum antigen titre. Treatment of serum samples with p
ronase substantially increased the sensitivity of the LCAT.