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Journal of Clinical Microbiology, April 1999, p. 1233-1233, Vol. 37, No. 4
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
LETTERS TO THE EDITOR
Study of False Positivity of Two Rapid Antigen Detection Tests
for Diagnosis of Plasmodium falciparum Malaria
 |
LETTER |
Presently, two rapid antigen detection tests are available for the
diagnosis of Plasmodium falciparum malaria (ParaSight F; Becton Dickinson, Tropical Disease Diagnostics, Sparks, Md., and ICT
Malaria Pf; ICT Diagnostics, Sydney, Australia). Both these tests are
based on the detection of histidine-rich protein 2 (HRP-2) antigen,
secreted by asexual stages of P. falciparum. Both the ParaSight F and ICT Malaria Pf tests have been reported as highly sensitive and specific by several authors (1, 4). Recently, however, false-positive test results with rheumatoid factor
(RF)-positive samples have been reported by investigators using the
ParaSight F kit (2). This prompted us to carry out a
comparative study between these two available tests to determine the
status of false positivity in RF-positive patients.
We tested blood samples of 25 RF-positive patients (2 were positive for
both RF and antinuclear antibody) who were negative for the malaria
parasite by Giemsa-stained thick-smear examination. ParaSight F tests
were falsely positive for 60% (15 of 25) of patients, a result which
is comparable to the finding of Laferl et al. (2) (67%
false positive). All 25 samples were tested in parallel by the ICT
Malaria Pf test. None of these samples were falsely positive.
No correlation between ParaSight F positivity and the titer of RF, the
type of collagen disease, or the age or sex of the patients was found.
The RF titer had no correlation with the intensity of the color on the strips.
The ParaSight F and ICT strips were used to test 20 smear-positive
P. falciparum samples. Both systems showed positive bands for all 20 samples. In addition to this, samples from 15 patients with
smear-positive P. vivax malaria, 1 patient with
P. malariae malaria, 4 with kala-azar, four with
tuberculosis, and six with typhoid fever were tested in parallel by
both tests. ParaSight F and ICT gave consistently negative results for
all these samples.
The discrepancy between the results of these two tests in the presence
of RF could be due to the nature of the capture monoclonal antibody
(Ab) on the strip. In the ParaSight F test, the coated Ab is
immunoglobulin G1 (IgG1) (1). Nonspecific attachment of RF
may be responsible for false-positive results. The capture monoclonal
antibody in the ICT test is IgM (3), to which RF does not
bind, thus there is no false positivity.
 |
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| | | | |
Baijayantimala Mishra
Jyotish Chandra Samantaray
Ashok Kumar
Bijay Ranjan Mirdha
All India Institute of Medical Sciences New Delhi 110029, India
|
Journal of Clinical Microbiology, April 1999, p. 1233-1233, Vol. 37, No. 4
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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