53,54 At 4��C DBS storage, measles antibody and EBV IgA www.selleckchem.com/products/carfilzomib-pr-171.html and IgG were stable for at least 24 weeks.49,52 Malaria. For the diagnosis and speciation of malaria, we found no evaluations of commercially available DBS assays using PCR in peer-reviewed journals. Two studies compared PCR on DBS against liquid whole blood and found a lower sensitivity, particularly for samples with low parasitaemia55,56 (Table 3). DBS PCR compared with microscopy achieves comparable performance or in some studies, is more sensitive.57 However, DBS PCR has a lower sensitivity than PCR on whole blood. Because both DBS PCR and microscopy may miss low-level parasitemia that whole-blood PCR detects, DBS PCR seems to have a higher specificity than whole-blood PCR. This result is because of the imperfect nature of the gold standard of microscopy.

56,58 Based on 10 papers included in this review, malaria detection using the nested PCR on DBS by Snounou and others59 seemed to be a suitable alternative to microscopy. DBS are also commonly used for detection of malaria resistance molecular markers.60 Table 3 Summary of studies evaluating DBS for malaria (malaria NAAT assays) Parasites. Non-malarial parasites cause many neglected tropical diseases afflicting hundreds of millions of people, predominantly in resource-poor regions with limited access to diagnostic facilities.61 The potential use of filter paper to aid diagnosis and understanding of the epidemiology of these diseases is, thus, very attractive. The mapping of lymphatic filariasis and monitoring of elimination programs provide an ideal role for DBS.

Three recent studies evaluated serological tests for Wuchereria bancrofti Og4C3 antigen on DBS compared with serum, giving sensitivities of > 93% and specificities of 82�C100%62�C64 (Table 4). An early study performed in Ghana reported a lower sensitivity (50%),65 possibly because of a difference in strain type (most other studies were performed in Asia), an assay cutoff that was set too high, or insufficient blood volume spotted onto filter paper. The CELISA (Cellabs Pty Ltd, Manly, Australia) (W. bancrofti and Brugia spp.) and Brugia Rapid (Reszon Diagnostics, Selangor, Malaysia) (Brugia spp.) tests performed on DBS eluate and compared with serum or plasma proved reasonably sensitive (71�C98%).66,67 Nucleic acid testing was evaluated for DBS versus microscopy for Brugian Brefeldin_A filariasis and Loa loa and seems sensitive, particularly for the latter at 96%.68�C70 African and American trypanosomiases have both been successfully diagnosed on DBS with high sensitivity and specificity,71�C74 but the sample size for Trypanosoma cruzi was relatively small.