Em. Haller et al., EVALUATION OF 2 NONCULTURE ANTIGEN TESTS AND 3 SEROTESTS FOR DETECTION OF ANTI-CHLAMYDIAL ANTIBODIES IN THE DIAGNOSIS OF OCULAR CHLAMYDIAL INFECTIONS, Graefe's archive for clinical and experimental ophthalmology, 234(8), 1996, pp. 510-514
Background: Diagnosis of chlamydial conjunctivitis is difficult in chr
onic diseases because chlamydial elementary bodies are mostly undetect
able in conjunctival scrapings by cell culture. We therefore compared
two nonculture antigen tests and three different serotests for anti-ch
lamydial antibodies with McCoy cell culture, the ''gold standard'' of
chlamydial diagnosis. Conjunctival scrapings and serum samples of 93 p
atients attending the outpatient eye clinic in Graz because of chronic
follicular conjunctivitis were tested. Methods: A total of 558 conjun
ctival scrapings and 93 serum samples were investigated. Chlamydial an
tigen detection was done by McCoy cell culture, polymerase chain react
ion (PCR; Amplicor, Roche), and direct immunofluorescence assay (DFA;
Microtrak, Syva). Antichlamydial IgA and IgG antibodies in the sera we
re detected by an immunoperoxidase assay (IPAzyme, Savyon) and two dif
ferent enzyme-linked immunosorbent assays (SeroELISA, Savyon and rELIS
A, medac). Results: Cell culture and PCR yielded identical results. Th
e positivity rate for chlamydial conjunctivitis was 8.6% (8 of 93 pati
ents). PCR proved most sensitive and most specific. IPAzyme was 75% se
nsitive for IgA and 100% for IgG; SeroELISA and rELISA were less sensi
tive. IPAzyme was 81% specific for IgA and 47.3% for IgG. SeroELISA an
d rELISA were less specific for IgA, but more specific for IgG. Post-t
est likelihood of disease was greatest in IPAzyme. Conclusions: PCR pr
oved to be a good alternative to cell culture; DFA is useful for quick
diagnosis. Genus-specific serotests cannot compete with chlamydial an
tigen detection. They differ in sensitivity and specificity because of
the antigen type they present. They are still of only supportive valu
e in cases where chlamydial antigen detection is not possible. Recentl
y introduced species-specific antibody tests should be of greater valu
e.