E. Kudo et al., DETECTION OF HERPES-SIMPLEX VIRUS-DNA IN TEAR FLUID OF STROMAL HERPETIC-KERATITIS PATIENTS BY NESTED POLYMERASE CHAIN-REACTION, Japanese Journal of Ophthalmology, 40(3), 1996, pp. 390-396
The value of the polymerase chain reaction (PCR) in the diagnosis of s
tromal herpetic keratitis was examined using tear fluid specimens; the
sensitivity of the nested PCR method in detecting the herpes simplex
virus (HSV) genome was 1 plaque-forming unit/mL. PCR assay of 72 tear
samples from the eyes of 15 patients with stromal herpetic keratitis d
etected the HSV genome in 5 (33.3%). No positive band was detected in
20 tear samples from both eyes of 10 healthy volunteers. Seven of 38 t
ear samples (18.4%) and 1 of 34 samples (2.9%) collected from the dise
ased eye and the contralateral normal eye, respectively, produced posi
tive results; the difference in rates was statistically significant (P
<0.05). The positive rate of samples collected from the diseased eye
during an active phase was 16.0% (4 of 25 samples); in the quiescent p
hase, 23.1% (3 of 13 samples); the difference was not significant (P=0
.45). In HSV genome-positive cases, the average number of tear collect
ions needed to detect the HSV genome was 3.3. Results indicate that PC
R assay of tear fluid provides valuable information for the diagnosis
of stromal herpetic keratitis, and that repeated tear samples should b
e collected regardless of the phase of disease activity.