Table 5.
Method | Principle | Sample | Sensitivity | Specificity | Advantages | Disadvantages |
---|---|---|---|---|---|---|
Western blot |
Western blot HSV-1 |
Serum |
≈100% |
≈100% |
Reference (“gold standard”) test proposed by University of Washington (USA) |
Not commercially available |
Expensive | ||||||
[UW-WB] | ||||||
Specific of HSV-1 and HSV-2 |
2–3 days for results |
|||||
Western blot HSV-2 | ||||||
Detect early sero-conversion to HSV-2 in patient with prior HSV-1 infection | ||||||
Earliest sero-conversion : 13 days | ||||||
Enzyme immune-assay |
Monoclonal antibody-blocking EIA |
Serum’ |
≈100% |
≈100% |
Reference (“gold standard”) test proposed by the Central Public Health Laboratory in the United Kingdom; 98% concordance with WU-WB |
Not commercially available |
(African sera : 98%) |
(African sera : 97%) |
|||||
Distinguish between HSV-1 and HSV-2 | ||||||
Enzyme immune-assay |
ELISA |
Serum |
93–98% |
93–99% |
Commercially available |
May lack of sensitivity and specificity |
Distinguish between HSV-1 and HSV-2 |
Lack of specific on African sera |
|||||
Point of care tests |
Immuno-filtration |
Serum Capillaryblood |
96% |
87–98% |
Less expensive than Western blot |
Commercially available only for HSV-2 |
Accurate results rapidly (6 min.) |
Expensive |
|||||
Not for large volume screening | ||||||
Easily to carry out | ||||||
Detects seroconversion within 4 weeks of presentation of 80% of patients with HSV-2 episodes | Complexity nonwaived (moderate) |
ELISA:Enzyme-linked immunosorbent assay; EIA: Enzyme immunoassay;
UW-WB: Western blot test developed at the University of Washington.