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Ouma C Davenport GC Garcia S Kempaiah P Chaudhary A Were T Anyona SB Raballah E Konah SN Hittner JB Vulule JM Ong'echa JM Perkins DJ 《Human genetics》2012,131(2):289-299
Development of protective immunity against Plasmodium falciparum is partially mediated through binding of malaria-specific IgG to Fc gamma (γ) receptors. Variations in human FcγRIIA-H/R-131 and FcγRIIIB-NA1/NA2 affect differential binding of IgG sub-classes. Since variability in FcγR may play an important role in severe malarial anemia (SMA) pathogenesis by mediating phagocytosis of red blood cells and triggering cytokine production, the relationship between FcγRIIA-H/R131 and FcγRIIIB-NA1/NA2 haplotypes and susceptibility to SMA (Hb?6.0?g/dL) was investigated in Kenyan children (n?=?528) with acute malaria residing in a holoendemic P. falciparum transmission region. In addition, the association between carriage of the haplotypes and repeated episodes of SMA and all-cause mortality were investigated over a 3-year follow-up period. Since variability in FcγR can alter interferon (IFN)-γ production, a mediator of innate and adaptive immune responses, functional associations between the haplotypes and IFN-γ were also explored. During acute malaria, children with SMA had elevated peripheral IFN-γ levels (P?=?0.006). Although multivariate logistic regression analyses (controlling for covariates) revealed no associations between the FcγR haplotypes and susceptibility to SMA during acute infection, the FcγRIIA-131H/FcγRIIIB-NA1 haplotype was associated with decreased peripheral IFN-γ (P?=?0.046). Longitudinal analyses showed that carriage of the FcγRIIA-131H/FcγRIIIB-NA1 haplotype was associated with reduced risk of SMA (RR 0.65, 95% CI 0.46-0.90; P?=?0.012) and all-cause mortality (P?=?0.002). In contrast, carriers of the FcγRIIA-131H/FcγRIIIB-NA2 haplotype had increased susceptibility to SMA (RR 1.47, 95% CI 1.06-2.04; P?=?0.020). Results here demonstrate that variation in the FcγR gene alters susceptibility to repeated episodes of SMA and mortality, as well as functional changes in IFN-γ production. 相似文献
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Kempaiah P Anyona SB Raballah E Davenport GC Were T Hittner JB Ong'echa JM Perkins DJ 《Human genetics》2012,131(8):1375-1391
Severe malarial anemia (SMA) is a leading cause of pediatric morbidity and mortality in holoendemic Plasmodium falciparum transmission areas. Although dysregulation in cytokine production is an important etiology of SMA, the role of IFN-α in SMA has not been reported. As such, we investigated the relationship between IFN-α promoter polymorphisms [i.e., IFNA2 (A-173T) and IFNA8 (T-884A)], SMA, and functional changes in IFN-α production in children (n = 663; <36 months) residing in a holoendemic P. falciparum transmission region of Kenya. Children with SMA had lower circulating IFN-α than malaria-infected children without severe anemia (P = 0.025). Multivariate logistic regression analyses revealed that heterozygosity at -884 (TA) was associated with an increased risk of SMA [OR 2.80 (95 % CI 1.22-6.43); P = 0.015] and reduced IFN-α relative to wild type (TT; P = 0.038). Additional analyses demonstrated that carriage of the -173T/-884A (TA) haplotype was associated with increased susceptibility to SMA [OR 3.98 (95 % CI 1.17-13.52); P = 0.026] and lower IFN-α (P = 0.031). Follow-up of these children for 36 months revealed that carriers of TA haplotype had greater all-cause mortality than non-carriers (P < 0.001). Generation of reporter constructs showed that the IFNA8 wild-type -884TT exhibited higher levels of luciferase expression than the variant alleles (P < 0.001). Analyses of malaria-associated inflammatory mediators demonstrated that carriers of TA haplotype had altered production of IL-1β, MIG, and IL-13 compared to non-carriers (P < 0.050). Thus, variation at IFNA2 -173 and IFNA8 -884 conditions reduced IFN-α production, and increased susceptibility to SMA and mortality. 相似文献
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Stefano Cannicci Farid Dahdouh-Guebas Dyane Anyona Marco Vannini 《Ethology : formerly Zeitschrift fur Tierpsychologie》1995,100(3):242-252
On the Kenyan coast, Thalamita crenata confines itself to a defined system of crevices and forages, swimming in a few cm of water, within a radius of about 5 m from its shelter. A field study was designed to analyse this crab's ability to find its shelter after being moved away from it. Crabs were displaced, being kept under water, with full vision of the sky and landscape and released 5 m away from their refuges, at a maximum depth of 50 cm. They were able to return to their shelters within 1 h and followed initial directions which were well orientated towards home. T. crenata was still well orientated and successful in returning home during nocturnal displacements and even after trials in which the landscape was altered. Only blind crabs were neither initially orientated towards home nor successful in returning within two tidal cycles of their release. The hypothesis that this swimming crab could use orientating information obtained during the outward displacement was then tested. Specimens were dislocated following a non-linear outward path, without vision of the surrounding landscape; other crabs were carried to a false release point and then carried in a closed container to the actual release point. Finally, three kinds of detour experiments were performed. In all these trials the directions chosen by the crabs were still clustered around the home direction and homing success was again high. These results exclude homing mechanisms based on random search strategies or on egocentric mechanisms, such as path integration. The most probable hypothesis is that T. crenata organizes some visual cues in a map-like arrangement and, detecting these cues from any release point within its home range, uses this map to return home. 相似文献
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John N. Waitumbi Samuel B. Anyona Carol W. Hunja Carolyne M. Kifude Mark E. Polhemus Douglas S. Walsh Chris F. Ockenhouse D. Gray Heppner Jr Amanda Leach Marc Lievens W. Ripley Ballou Joe D. Cohen Colin J. Sutherland 《PloS one》2009,4(11)
Objective
RTS,S, a candidate vaccine for malaria, is a recombinant protein expressed in yeast containing part of the circumsporozoite protein (CSP) sequence of 3D7 strain of Plasmodium falciparum linked to the hepatitis B surface antigen in a hybrid protein. The RTS,S antigen is formulated with GSK Biologicals'' proprietary Adjuvant Systems AS02A or AS01B. A recent trial of the RTS,S/AS02A and RTS,S/AS01B vaccines evaluated safety, immunogenicity and impact on the development of parasitemia of the two formulations. Parasite isolates from this study were used to determine the molecular impact of RTS,S/AS02A and RTS,S/AS01B on the multiplicity of infection (MOI) and the csp allelic characteristics of subsequent parasitemias.Design
The distribution of csp sequences and the MOI of the infecting strains were examined at baseline and in break-through infections from vaccinated individuals and from those receiving a non-malarial vaccine.Setting
The study was conducted in Kombewa District, western Kenya.Participants
Semi-immune adults from the three study arms provided isolates at baseline and during break-through infections.Outcome
Parasite isolates used for determining MOI and divergence of csp T cell–epitopes were 191 at baseline and 87 from break-through infections.Results
Grouping recipients of RTS,S/AS01A and RTS,S/AS02B together, vaccine recipients identified as parasite-positive by microscopy contained significantly fewer parasite genotypes than recipients of the rabies vaccine comparator (median in pooled RTS,S groups: 3 versus 4 in controls, P = 0.0313). When analyzed separately, parasitaemic individuals in the RTS,S/AS01B group, but not the RTS,S/AS02A group, were found to have significantly fewer genotypes than the comparator group. Two individual amino acids found in the vaccine construct (Q339 in Th2R and D371 in Th3R) were observed to differ in incidence between vaccine and comparator groups but in different directions; parasites harboring Q339 were less common among pooled RTS,S/AS vaccine recipients than among recipients of rabies vaccine, whereas parasites with D371 were more common among the RTS,S/AS groups.Conclusions
It is concluded that both RTS,S/AS vaccines reduce multiplicity of infection. Our results do not support the hypothesis that RTS,S/AS vaccines elicit preferential effects against pfcsp alleles with sequence similarity to the 3D7 pfcsp sequence employed in the vaccine construct. 相似文献6.
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