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1 donors were stimulated in vitro with soluble microfilarial Ag (MfAg) from the filarial parasite Brugi
3 gen-specific IL-5 production, and diminished microfilarial antigen-driven lymphocyte proliferation th
4 ve interleukin-5 (IL-5) and IL-10, increased microfilarial antigen-specific IL-5 production, and dimi
6 tervention-naive areas with 30%, 50%, or 70% microfilarial baseline prevalence (representative of hyp
8 ly and positively associated with increasing microfilarial burden (p<0.00001), but not with blindness
9 s combination (IDA) has improved efficacy of microfilarial clearance at 12 months in individually ran
11 n subjects with loiasis and had no effect on microfilarial clearance, the reduction in AEC appeared t
18 refore aimed to investigate changes in L loa microfilarial densities during TaNT campaigns run 18 mon
19 investigates the relationship between L. loa microfilarial density (Loa MFD) and the probability of t
20 However, the presence of MF (rho = 0.45) and microfilarial density (rho = 0.44) were significantly co
21 ivermectin distribution because of an L. loa microfilarial density above the risk threshold, and 397
22 was used to identify persons with an L. loa microfilarial density greater than 20,000 microfilariae
23 ivermectin treatment because of a high L loa microfilarial density in 2015, versus 283 (1.5%) individ
26 essed in all participants, was whether L loa microfilarial density was above or below the exclusion t
28 licable as a point-of-care method for L. loa microfilarial detection and quantification in resource-l
29 re and in 7 subjects with evidence of dermal microfilarial DNA and were compared with responses in 43
31 We evaluated Onchocerca volvulus community microfilarial intensity and prevalence in persons aged >
32 n treatment in Ghana has reduced O. volvulus microfilarial intensity and prevalence, but suboptimal r
33 e shown a direct relation between O volvulus microfilarial load and host mortality in a comprehensive
37 d an association between Onchocerca volvulus microfilarial load in childhood and risk of developing e
39 iasis has insufficient sensitivity when skin microfilarial (mf) densities are low, such as following
40 directed primarily against the intravascular microfilarial (MF) parasite stage and mediated in part b
43 cific serpin in the blood environment of the microfilarial parasite in protection from human immunity
45 We use the EPIONCHO-IBM model to project microfilarial prevalence trends across Togo's five regio
46 f at least one of the following assessments: microfilarial prevalence, nodule prevalence, Ov16 antibo
48 tin (standard) dose clears the skin-dwelling microfilarial progeny of adult worms (macrofilariae) and
53 itively associated with the village-specific microfilarial rate, mean intensity of microfilaremia, an
54 nal regression modeling to estimate rates of microfilarial repopulation of the skin in a cohort of 21
55 e did not find any clear association between microfilarial repopulation rate and the number of years
60 elicit high levels of host IL-4 whereas the microfilarial stage of the parasite induces IFN-gamma pr
62 age colony-stimulating factor) to adult- and microfilarial-stage antigens, but not antibody responses