Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/310
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dc.contributor.authorNg'ang'a, Zipporah W.
dc.contributor.authorKiptoo, Michael K.
dc.contributor.authorMpoke, Solomon S.
dc.contributor.authorOsman, Saida
dc.contributor.authorMwangi, Ann
dc.contributor.authorSongok, Elijah M.
dc.date.accessioned2014-12-03T11:22:10Z
dc.date.available2014-12-03T11:22:10Z
dc.date.issued2009
dc.identifier.citationInternational Journal of Integrative Biology 01/2009en_US
dc.identifier.issn09738363
dc.identifier.urihttp://www.researchgate.net/publication/228759302_Indirect_Immunofluorescence_assay_Particle_Agglutination_and_ELISA_for_the_detection_of_HIV_type
dc.identifier.urihttp://hdl.handle.net/123456789/310
dc.description.abstractScreening of blood and blood products for human immunodeficiency virus (HIV) is routinely performed using the enzyme-linked immunosorbent assay (ELISA), and the results confirmed by western blot (WB). In an effort to identify alternative techniques, two locally prepared test kits were evaluated to determine the performance in comparison to commercial kits. These diagnostic kits were indirect immunofluorescence assay (IFA) and particle agglutination (PA). Blood obtained from 400 patients seeking treatment for sexually transmitted infections (STI) at a special treatment clinic in Nairobi were tested for ant-HIV-1 antibody by ELISA, PA and IFA. Out of 160 samples that were HIV antibody positive by PA, 10 (6.3%) were HIV antibody negative by IFA. Out of 240 samples that were HIV antibody negative by PA, 1(0.4%) was HIV antibody positive by IFA. The IFA results agreed with those of PA with a consistency of 97.3% (389 out of 400). The sensitivity and specificity of IFA was 99.3% and 95.9% respectively. Out of 170 samples that were HIV antibody positive by ELISA, 22 (5.8%) were HIV antibody negative by IFA. The IFA results agreed with those of ELISA with a consistency of 93.8% (375 out of 400). The sensitivity and specificity of IFA was 98.0% and 91.2% respectively. This study demonstrates that PA can be used for epidemiological studies and as a screening test in resource poor settings.en_US
dc.language.isoenen_US
dc.publisherIJIBen_US
dc.subjectParticle agglutination assayen_US
dc.subjectImmunoflourescence assayen_US
dc.subjectSensitivityen_US
dc.subjectSpecificityen_US
dc.subjectDiagnosisen_US
dc.subjectHIVen_US
dc.titleIndirect immunofluorescence assay, particle agglutination and ELISA for the detection of HIV type 1en_US
dc.typeArticleen_US
Appears in Collections:School of Science and Computing (JA)

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