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81.
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83.
Chukwujindu M. A. Iwegbue Godwin E. Nwajei Osayanmo I. Eguavoen 《Soil & Sediment Contamination》2012,21(1):19-30
The study of the concentrations of Cr, Zn, Cd, Pb, Ni, and Cu in soils under different land uses in rural, semi-urban, and urban zones in the Niger Delta was carried out with a view to providing information on the effects of the different land uses on the concentrations of trace elements in soils. Our results indicate significant variability in concentrations of these metals in soils under different land uses in rural, semi-urban, and urban zones. The maximum concentrations of metals in the examined soil samples were 707.5 mg.kg?1, 161.0 mg.kg?1, 2.6 mg.kg?1, 59.6 mg.kg?1, 1061.3 mg.kg?1, and 189.2 mg.kg?1 for Cr, Zn, Cd, Pb, Ni, and Cu, respectively. In the rural zone, the cassava processing mill is a potent source of Ni, Cr, Cu, and Zn while agricultural activities are a source of Cd, and automobile emissions and the use of lead oxide batteries constitute the major sources of Pb. In the urban zone, soils around the wood processing mill showed elevated concentrations of Cu, Cr, Zn, and Ni, while soils around automobile mechanic works and motor parks showed elevated levels of Pb. Elevated Cd concentrations were observed in soils under the following land uses: urban motor park, playground, welding and fabrication sheds, and metallic scrap dump. The contamination/pollution index of metals in the soil follows the order: Ni > Cd > Cr > Zn > Cu > Pb. The multiple pollution index of metals at different sites were greater than 1, indicating that these soils fit into “slight pollution” to “excessive pollution” ranges with significant contributions from Cr, Zn, Cd, Ni, and Cu. 相似文献
84.
Akinsola AK Ota MO Enwere GC Okoko BJ Zaman SM Saaka M Nsekpong ED Odutola AA Greenwood BM Cutts FT Adegbola RA 《PloS one》2012,7(2):e31050
Background
A 9-valent pneumococcal conjugate vaccine (PCV-9), given in a 3-dose schedule, protected Gambian children against pneumococcal disease and reduced nasopharyngeal carriage of pneumococci of vaccine serotypes. We have studied the effect of a booster or delayed primary dose of 7-valent conjugate vaccine (PCV-7) on antibody and nasopharyngeal carriage of pneumococci 3–4 years after primary vaccination.Methodology/Principal Findings
We recruited a subsample of children who had received 3 doses of either PCV-9 or placebo (controls) into this follow-up study. Pre- and post- PCV-7 pneumococcal antibody concentrations to the 9 serotypes in PCV-9 and nasopharyngeal carriage of pneumococci were determined before and at intervals up to 18 months post-PCV-7. We enrolled 282 children at a median age of 45 months (range, 38–52 months); 138 had received 3 doses of PCV-9 in infancy and 144 were controls. Before receiving PCV-7, a high proportion of children had antibody concentrations >0.35 µg/mL to most of the serotypes in PCV-9 (average of 75% in the PCV-9 and 66% in the control group respectively). The geometric mean antibody concentrations in the vaccinated group were significantly higher compared to controls for serotypes 6B, 14, and 23F. Antibody concentrations were significantly increased to serotypes in the PCV-7 vaccine both 6–8 weeks and 16–18 months after PCV-7. Antibodies to serotypes 6B, 9V and 23F were higher in the PCV-9 group than in the control group 6–8 weeks after PCV-7, but only the 6B difference was sustained at 16–18 months. There was no significant difference in nasopharyngeal carriage between the two groups.Conclusions/Significance
Pneumococcal antibody concentrations in Gambian children were high 34–48 months after a 3-dose primary infant vaccination series of PCV-9 for serotypes other than serotypes 1 and 18C, and were significantly higher than in control children for 3 of the 9 serotypes. Antibody concentrations increased after PCV-7 and remained raised for at least 18 months. 相似文献85.
R Hashim AM Khatib G Enwere JK Park R Reyburn M Ali NY Chang DR Kim B Ley K Thriemer AL Lopez JD Clemens JL Deen S Shin C Schaetti R Hutubessy MT Aguado MP Kieny D Sack S Obaro AJ Shaame SM Ali AA Saleh L von Seidlein MS Jiddawi 《PLoS neglected tropical diseases》2012,6(7):e1743
Introduction
Mass vaccinations are a main strategy in the deployment of oral cholera vaccines. Campaigns avoid giving vaccine to pregnant women because of the absence of safety data of the killed whole-cell oral cholera (rBS-WC) vaccine. Balancing this concern is the known higher risk of cholera and of complications of pregnancy should cholera occur in these women, as well as the lack of expected adverse events from a killed oral bacterial vaccine.Methodology/Principal Findings
From January to February 2009, a mass rBS-WC vaccination campaign of persons over two years of age was conducted in an urban and a rural area (population 51,151) in Zanzibar. Pregnant women were advised not to participate in the campaign. More than nine months after the last dose of the vaccine was administered, we visited all women between 15 and 50 years of age living in the study area. The outcome of pregnancies that were inadvertently exposed to at least one oral cholera vaccine dose and those that were not exposed was evaluated. 13,736 (94%) of the target women in the study site were interviewed. 1,151 (79%) of the 1,453 deliveries in 2009 occurred during the period when foetal exposure to the vaccine could have occurred. 955 (83%) out of these 1,151 mothers had not been vaccinated; the remaining 196 (17%) mothers had received at least one dose of the oral cholera vaccine. There were no statistically significant differences in the odds ratios for birth outcomes among the exposed and unexposed pregnancies.Conclusions/Significance
We found no statistically significant evidence of a harmful effect of gestational exposure to the rBS-WC vaccine. These findings, along with the absence of a rational basis for expecting a risk from this killed oral bacterial vaccine, are reassuring but the study had insufficient power to detect infrequent events.Trial Registration
ClinicalTrials.gov NCT00709410相似文献86.
Kamdem Toukam D Tenbusch M Stang A Temchura V Storcksdieck Genannt Bonsmann M Grewe B Koch S Meyerhans A Nchinda G Kaptue L Uberla K 《PloS one》2012,7(5):e38068
Although human immunodeficiency type 1 (HIV-1) infection induces strong antibody responses to the viral envelope glycoprotein (Env) only a few of these antibodies possess the capacity to neutralize a broad range of strains. The induction of such antibodies represents an important goal in the development of a preventive vaccine against the infection. Among the broadly neutralizing monoclonal antibodies discovered so far, three (2F5, Z13 and 4E10) target the short and hidden membrane proximal external region (MPER) of the gp41 transmembrane protein. Antibody responses to MPER are rarely observed in HIV-infected individuals or after immunization with Env immunogens. To initiate antibody responses to MPER in its membrane-embedded native conformation, we generated expression plasmids encoding the membrane-anchored ectodomain of gp41 with N-terminal deletions of various sizes. Following transfection of these plasmids, the MPER domains are displayed on the cell surface and incorporated into HIV virus like particles (VLP). Transfected cells displaying MPER mutants bound as efficiently to both 2F5 and 4E10 as cells transfected with a plasmid encoding full-length Env. Mice immunized with VLPs containing the MPER mutants produced MPER-specific antibodies, the levels of which could be increased by the trimerization of the displayed proteins as well as by a DNA prime-VLP boost immunization strategy. Although 2F5 competed for binding to MPER with antibodies in sera of some of the immunized mice, neutralizing activity could not be detected. Whether this is due to inefficient binding of the induced antibodies to MPER in the context of wild type Env or whether the overall MPER-specific antibody response induced by the MPER display mutants is too low to reveal neutralizing activity, remains to be determined. 相似文献
87.
Fos C Salles A Lang V Carrette F Audebert S Pastor S Ghiotto M Olive D Bismuth G Nunès JA 《Journal of immunology (Baltimore, Md. : 1950)》2008,181(3):1969-1977
ICOS ligation in concert with TCR stimulation results in strong PI3K activation in T lymphocytes. The ICOS cytoplasmic tail contains an YMFM motif that binds the p85alpha subunit of class IA PI3K, similar to the YMNM motif of CD28, suggesting a redundant function of the two receptors in PI3K signaling. However, ICOS costimulation shows greater PI3K activity than CD28 in T cells. We show in this report that ICOS expression in activated T cells triggers the participation of p50alpha, one of the regulatory subunits of class IA PI3Ks. Using different T-APC cell conjugate systems, we report that p50alpha accumulates at the immunological synapse in activated but not in resting T cells. Our results demonstrate that ICOS membrane expression is involved in this process and that p50alpha plasma membrane accumulation requires a functional YMFM Src homology 2 domain-binding motif in ICOS. We also show that ICOS triggering with its ligand, ICOSL, induces the recruitment of p50alpha at the synapse of T cell/APC conjugates. In association with the p110 catalytic subunit, p50alpha is known to carry a stronger lipid kinase activity compared with p85alpha. Accordingly, we observed that ICOS engagement results in a stronger activation of PI3K. Together, these findings provide evidence that p50alpha is likely a determining factor in ICOS-mediated PI3K activity in T cells. These results also suggest that a differential recruitment and activity of class IA PI3K subunits represents a novel mechanism in the control of PI3K signaling by costimulatory molecules. 相似文献
88.
The water-soluble, biocompatible polymer poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) was evaluated for protein conjugation. PMPC is a zwitterionic polymer that is able to form a more compact conformation in aqueous solution than poly(ethylene glycol) (PEG). While a terminally functionalized N-hydroxysuccinimide derivative of PMPC was not efficient for conjugation to an amine moiety on interferon-alpha2a (IFN), we found that a bis-thiol specific derivative of PMPC could be conjugated after reduction of the disulfide bonds in IFN. Utilizing PMPC that displayed a similar hydrodynamic volume to 20 kDa PEG, we evaluated the in vitro antiviral and antiproliferative activity and pharmacokinetics of a PMPC-IFN conjugate. As a hygroscopic zwitterionic polymer, PMPC is able to form a compact conformation in aqueous solution, which was found to be more compact than PEG. This suggests that PMPC protein conjugates may display different plasma elimination characteristics than PEG protein conjugates. PMPC-IFN displayed marked resistance to antibody binding in Western blot analysis with a polyclonal anti-IFN antibody while displaying comparable in vitro antiviral and antiproliferative activity to PEG-IFN. During an in vivo pharmacokinetic study, the absorption t(1/2) for PMPC-IFN was considerably extended compared to the native IFN and 20 kDa PEG analogue. This is also consistent with the SDS-PAGE result where an apparent reduction in mobility through a hydrated medium was observed. The elimination t(1/2) was also vastly extended over the native IFN and twice the value of 20 kDa PEG-IFN. This suggests that tissue migration of PMPC-IFN occurs more slowly than the 20 kDa PEG-IFN despite their similarity in hydrodynamic volume, leading to an an improved depot effect, which could explain the longer elimination t(1/2). In this study, we demonstrate a potential use of PMPCylation as a novel tool for enhancing the pharmacokinetic profile of therapeutic proteins in ways that complement PEGylation. 相似文献
89.
Jordan D. R. Tao Y. Z. Godwin I. D. Henzell R. G. Cooper M. McIntyre C. L. 《Molecular breeding : new strategies in plant improvement》2005,14(4):441-454
Seventy sorghum inbred lines which formed part of the Queensland Department of Primary Industries (QDPI) sorghum breeding program were screened with 104 previously mapped RFLP markers. The lines were related by pedigree and consisted of ancestral source lines, intermediate lines and recent releases from the program. We compared the effect of defining marker alleles using either identity by state (IBS) or identity by descent (IBD) on our capacity to trace markers through the pedigree and detect evidence of selection for particular alleles. Allelic identities defined using IBD were much more sensitive for detecting non-Mendelian segregation in this pedigree. Only one marker allele showed significant evidence of selection when IBS was used compared with ten regions with particular allelic identities when IBD was used. Regions under selection were compared with the location of QTLs for agronomic traits known to be under selection in the breeding program. Only two of the ten regions were associated with known QTLs that matched with knowledge of the agronomic characteristics of the ancestral lines. Some of the other regions were hypothesised to be associated with genes for particular traits based on the properties of the ancestral source lines. 相似文献
90.
Valerie S. Calvert Yihui Tang Vince Boveia Julie Wulfkuhle Amy Schutz-Geschwender D. Michael Olive Lance A. Liotta Emanuel F. Petricoin III 《Clinical proteomics》2004,1(1):81-89
Protein microarrays have been recently employed for signal pathway profiling and high-throughput protein expression analysis.
Reversephase arrays, where the array consists of immobilized analytes and lysates has especially shown promise in low abundance
analyte detection and signal pathway profiling using phospho-specific antibodies. A limitation to current reverse phase array
methodology is the inability to multiplex proteomic-based endpoints as each array can only report one analyte endpoint. In
this study, we report on the use of a dual dye based approach that can effectively double the number of endpoints observed
per array allowing, for example, both phosphospecific and total protein levels to be measured and analyzed at once. The method
utilizes antibody bound dyes that emit in the infrared spectral region as a means of sensitive and specific detection. 相似文献