1978
DOI: 10.1080/00034983.1978.11719308
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The micro-ELISA technique in the serodiagnosis of visceral leishmaniasis

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Cited by 126 publications
(59 citation statements)
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“…These methods tend to be created according to the preferences of each laboratory, and may cause discordant results between different laboratories. In addition, crude antigen preparations made from whole promastigotes or their soluble extracts limit the standardization of testing and the reproducibility of results [26][27][28] . When using ELISA as a serological test, we found significantly conflicting results when different antigen preparations were used.…”
Section: Discussionmentioning
confidence: 99%
“…These methods tend to be created according to the preferences of each laboratory, and may cause discordant results between different laboratories. In addition, crude antigen preparations made from whole promastigotes or their soluble extracts limit the standardization of testing and the reproducibility of results [26][27][28] . When using ELISA as a serological test, we found significantly conflicting results when different antigen preparations were used.…”
Section: Discussionmentioning
confidence: 99%
“…The most frequently reported cross-reactions occur in areas where diseases such as Chagas' disease and African trypanosomiasis co-exist with kala-azar. 17,18 As these two diseases do not occur in Yemen, this was not a problem in our setting, but crossreactions from cutaneous leishmaniasis 19,20 can affect specificity, In spite of some reports of cross-reaction of anti-leishmania antibodies with malaria, TB, and Hansen's disease, [18][19][20][21][22] Choudhry at al. did not observe any such cross-reactions.…”
Section: Discussionmentioning
confidence: 99%
“…In order to develop specific assays for the serodiagnosis of leishmaniasis, several promastigote and amastigote antigens, purified antigens such as FML, defined, synthetic peptides or recombinant antigens have been characterized and evaluated. Among the many antigens used in ELISA for the diagnosis of leishmaniasis are total soluble antigen (Hommel et al 1978), dp72 Zalis 1988), gp 63 (Okong'o-Odera et al 1993), 78 kDa (Ravindran et al 2004) and rK39, a recombinant and a kinesin-related protein (Burns et al 1993). Some other antigens from L. infantum such as the acidic ribosomal proteins P2a and P2b, the ribosomal protein P0, the histones H2A (Soto et al 1995) and H3 were isolated and characterized for diagnosing canine VL.…”
Section: Discussionmentioning
confidence: 99%