|
By
Do Quang Ha, Cao
Minh Thang, Tran Ton, Vu thi Que Huong,
Huynh thi Kim Loan, Hoang thi
Nhu Dao and Tran thi Hue
Tam
Pasteur Institute, Ho Chi Minh
City,
Viet Nam
Table 5. Comparison of the CPD IgG
assays with the HAI and virus isolations*
|
Sera
|
CPD IgG
|
HAI
and Virus isolation
|
|
Positive
|
Sensitivity
|
Positive
|
Sensitivity
|
|
S1
|
41/53
|
77.36%
|
Inconclusive
|
|
|
S2
|
50/53
|
94.34%
|
|
|
|
Paired
sera
|
50/53
|
94.34%
|
50/53
|
94.34%
|
*By
the Chi-Squares Mantel-Haenszel, c 2 was 0.00, P
=0.660.
The specificity of the CPD IgM-IgG
Forty-two
single sera were taken on the day of admission from children with clinical
diagnosis as measles, out of which there were 25 positives and 17 negatives
by measles IgM capture-ELISA. These sera were
retested with CPD IgM-IgG and the Mac-ELISA, HAI
for dengue. The results are given in Table 6.
Table 6. Performance of CPD IgM
and Mac-ELISA with measles sera*
|
Measles
|
CPD IgM
|
Mac-ELISA
|
|
Mac-
ELISA
|
Negative
|
Specificity
|
Negative
|
Specificity
|
|
25 (+)
|
21/25
|
84%
|
25/25
|
100%
|
|
17 (-)
|
17/17
|
100%
|
17/17
|
100%
|
|
Total:
42 single sera
|
38/42
|
90.48%
|
42/42
|
100%
|
*By
the Chi-Squares Mantel-Haenszel, c 2 was 4.15, P
=0.058
Among
the 42 single sera, there were five sera having dengue antibody (³ 40 HAI
units), so we discarded them and only 37 measles sera without dengue antibody
were used for the specificity study of the CPD IgG.
Thirty-seven
measles sera without dengue antibody were tested with CPD IgG,
from which there were two false positive results and 35 negative. So, the CPD
IgG is specific to dengue IgG
with the rate of 94.59% (Table 7).
Table 7. Performance of the CPD IgG
and the HAI with measles sera without dengue antibody
|
Measles
|
CPD IgG
|
HAI
|
|
Mac-ELISA
|
Negative
|
Specificity
|
Negative
|
Specificity
|
|
21 (+)
|
21/21
|
100%
|
21/21
|
|
|
16 (-)
|
14/16
|
87.5%
|
16/16
|
|
|
Total:
37 single sera
|
35/37
|
94.59%
|
37/37
|
Inconclusive
|
Summation
The
total number of samples tested for CPD IgM and CPD IgG and their sensitivity and specificity are given
below:
|
Assay
evaluated
|
Sensitivity
|
Specificity
|
|
CPD IgM
|
98.11%
(52 of 53)
|
90.48%
(38 of 42)
|
|
CPD IgG
|
94.34%
(50 of 53)
|
94.59%
(35 of 37)
|
|
Mac-ELISA
|
98.11%
(52 of 53)
|
100%
(42 of 42)
|
|
HAI
(paired sera)
|
94.34%
(50 of 53)
|
Inconclusive
with single sera
|
The
CPD IgM-IgG evaluated in this report are suitable
for the detection of anti-dengue IgM and IgG antibodies. They should be useful for routine dengue
diagnosis, particularly in developing countries as in south-east Asia where dengue infections are
prevalent. For the prevention and control of dengue, the CPD IgM and the Mac-ELISA are good tools for the early
detection of dengue cases during the inter-epidemic period, or during the
pre-epidemic stage, for carrying out laboratory-based active surveillance.
Conclusion
The
Commercial Pathozyme Dengue IgM
and IgG are reliable, sensitive and specific
diagnostic tests for diagnosing primary and secondary dengue infections based
on antibody responses. It should be used in laboratories to support the
clinical diagnosis of dengue. The Commercial Pathozyme
Dengue IgM is also a very good tool for active
laboratory-based dengue surveillance with the aim of controlling dengue
epidemics in the tropical and sub-tropical regions.
References
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Quang Ha et al. (1993). Epidemiology of dengue in south VietNam
and the strategy of its control.Japan.
Trop. Med., 35 (4): 179-184.
2. Do
Quang Ha et al. (1996). Dengue haemorrhagic
fever in south VietNam,
1991-1994. Dengue Bulletin WHO 20: 55-61.
3. Gubler DJ (1996). Serological diagnosis of dengue/dengue haemorrhagic fever. Dengue Bull. 20: 20-23.
4. Innis, BL., Nisalak A, Nimmannitya S, Kusalerdchariya
S, Chongswasdi V, Suntayakorn
S, Puttisri P and Hoke CH
(1989). An enzyme-linked immunosorbent assay to
characterize dengue infections where dengue and Japanese encephalitis
co-circulate. Am. J. Trop. Med. 40: 418-427.
5. Clarke
DH, and Casals J (1958).
Techniques for haemagglutination and haemagglutination inhibition with arthropod-borne
viruses. Am. J. Trop. Med. Hyg. 7: 561-573.
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(1987): Detecting artificial anti-dengue IgM immune
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assay. Am. J. Trop. Med. Hyg., 36: 153-159.
7. World
Health Organization. (1986). Dengue haemorrhagic
fever diagnosis, treatment and control. WHO, Geneva,
Switzerland.

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