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Strong Human Immunodeficiency Virus (HIV)-Specific Cytotoxic T-Lymphocyte Activity in Sydney Blood Bank Cohort Patients Infected with nef-Defective HIV Type 1 总被引:2,自引:1,他引:1 下载免费PDF全文
Wayne B. Dyer Graham S. Ogg Marie-Ange Demoitie Xia Jin Andrew F. Geczy Sarah L. Rowland-Jones Andrew J. McMichael Douglas F. Nixon John S. Sullivan 《Journal of virology》1999,73(1):436-443
Proposals for the use of live attenuated human immunodeficiency virus (HIV) type 1 (HIV-1) as a vaccine candidate in humans have been based on the protection afforded by attenuated simian immunodeficiency virus in the macaque model. Although it is not yet known if this strategy could succeed in humans, a study of the Sydney Blood Bank Cohort (SBBC), infected with an attenuated HIV-1 quasispecies with natural nef and nef/long terminal repeat deletions for up to 17 years, could provide insights into the long-term immunological consequences of living with an attenuated HIV-1 infection. In this study, HIV-specific cytoxic T-lymphocyte (CTL) responses in an SBBC donor and six recipients were examined over a 3-year period with enzyme-linked immunospot, tetrameric complex binding, direct CTL lysis, and CTL precursor level techniques. Strong HIV-specific CTL responses were detected in four of seven patients, including one patient with an undetectable viral load. Two of seven patients had weak CTL responses, and in one recipient, no HIV-specific CTLs were detected. High levels of circulating effector and memory HIV-specific CTLs can be maintained for prolonged periods in these patients despite very low viral loads. 相似文献
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Agnandji ST Fendel R Mestré M Janssens M Vekemans J Held J Gnansounou F Haertle S von Glasenapp I Oyakhirome S Mewono L Moris P Lievens M Demoitie MA Dubois PM Villafana T Jongert E Olivier A Cohen J Esen M Kremsner PG Lell B Mordmüller B 《PloS one》2011,6(4):e18559
The recombinant circumsporozoite protein (CS) based vaccine, RTS,S, confers protection against Plasmodium falciparum infection in controlled challenge trials and in field studies. The RTS,S recombinant antigen has been formulated with two adjuvant systems, AS01 and AS02, which have both been shown to induce strong specific antibody responses and CD4 T cell responses in adults. As infants and young children are particularly susceptible to malaria infection and constitute the main target population for a malaria vaccine, we have evaluated the induction of adaptive immune responses in young children living in malaria endemic regions following vaccination with RTS,S/AS01(E) and RTS,S/AS02(D). Our data show that a CS-specific memory B cell response is induced one month after the second and third vaccine dose and that CS-specific antibodies and memory B cells persist up to 12 months after the last vaccine injection. Both formulations also induced low but significant amounts of CS-specific IL-2(+) CD4(+) T cells one month after the second and third vaccine dose, upon short-term in vitro stimulation of whole blood cells with peptides covering the entire CS derived sequence in RTS,S. These results provide evidence that both RTS,S/AS01(E) and RTS,S/AS02(D) induced adaptive immune responses including antibodies, circulating memory B cells and CD4(+) T cells directed against P. falciparum CS protein. TRIAL REGISTRATION: ClinicalTrials.gov NCT00307021. 相似文献
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Stéphane Mouilleron Marie-Ange Badet-Denisot Ludovic Pecqueur Karine Madiona Nadine Assrir Bernard Badet Béatrice Golinelli-Pimpaneau 《The Journal of biological chemistry》2012,287(41):34533-34546
The amino-terminal cysteine of glucosamine-6-phosphate synthase (GlmS) acts as a nucleophile to release and transfer ammonia from glutamine to fructose 6-phosphate through a channel. The crystal structure of the C1A mutant of Escherichia coli GlmS, solved at 2.5 Å resolution, is organized as a hexamer, where the glutaminase domains adopt an inactive conformation. Although the wild-type enzyme is active as a dimer, size exclusion chromatography, dynamic and quasi-elastic light scattering, native polyacrylamide gel electrophoresis, and ultracentrifugation data show that the dimer is in equilibrium with a hexameric state, in vitro and in cellulo. The previously determined structures of the wild-type enzyme, alone or in complex with glucosamine 6-phosphate, are also consistent with a hexameric assembly that is catalytically inactive because the ammonia channel is not formed. The shift of the equilibrium toward the hexameric form in the presence of cyclic glucosamine 6-phosphate, together with the decrease of the specific activity with increasing enzyme concentration, strongly supports product inhibition through hexamer stabilization. Altogether, our data allow us to propose a morpheein model, in which the active dimer can rearrange into a transiently stable form, which has the propensity to form an inactive hexamer. This would account for a physiologically relevant allosteric regulation of E. coli GlmS. Finally, in addition to cyclic glucose 6-phosphate bound at the active site, the hexameric organization of E. coli GlmS enables the binding of another linear sugar molecule. Targeting this sugar-binding site to stabilize the inactive hexameric state is therefore suggested for the development of specific antibacterial inhibitors. 相似文献
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Expression and purification of active human internal His(6)-tagged L-glutamine: D-Fructose-6P amidotransferase I 总被引:1,自引:0,他引:1
Richez C Boetzel J Floquet N Koteshwar K Stevens J Badet B Badet-Denisot MA 《Protein expression and purification》2007,54(1):45-53
Human L-glutamine: D-fructose-6-phosphate amidotransferase (Gfat1), a recognized target in type 2 diabetes complications, was expressed in Sf9 insect cells with an internal His(6)-tag and purified to homogenity. Two different microplate assays that quantify, respectively D-glucosamine-6-phosphate and L-glutamate were used to analyze the enzyme kinetic properties. The recombinant human L-glutamine: D-fructose-6-phosphate amidotransferase isoform 1 exhibits Michaelis parameters K(m)(Fru-6P)=0.98 mM and K(m)(Gln)=0.84 mM which are similar to the values reported for the same enzyme from different sources. The stimulation of hydrolysis of the alternate substrate L-glutamine para-nitroanilide by D-fructose-6P (Fru-6P) afforded a K(d) of 5 microM for Fru-6P. 相似文献
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Marie-Ange Gravel & Steven J. Cooke † 《Ethology : formerly Zeitschrift fur Tierpsychologie》2009,115(6):608-616
Predation risk has the ability to greatly influence the behaviour of reproducing individuals. In large long-lived species with low risk of predation for parents, reproductive behaviours often involve caring for offspring (i.e. defending broods from predators) and these behaviours are essential for offspring survival. Our objectives were to test for the presence of natural variation in nest predation pressure in an aquatic environment for a species that provides sole-paternal care, smallmouth bass ( Micropterus dolomieu ), and to determine if natural variation in predation pressure influences parental care behaviour. We used snorkeler observations and a series of metrics to assess predation pressure and parental care behaviour in six lakes within a narrow geographical range. Lakes differed in all predation pressure metrics: number of predators in proximity to nest when males were present, time to predator arrival and number of predators that consumed eggs when males were absent and total number of nests that was preyed upon. Similarly, parental behaviour varied between lakes. Parental smallmouth bass spent more time engaged in anti-predator defences in lakes with high predation pressure, while males from low predator pressure lakes remained close to their nest. Conversely, males from lakes with low and high predation pressure showed a similar willingness to defend their nests during simulated nest predation events. Our results show that natural variation in aquatic nest predation pressure across multiple lakes can be significant and has the ability to influence baseline parental care behaviour. Such variation provides opportunities to study the costs and consequences of parental care and to evaluate how this could influence demography and community interactions in aquatic systems. 相似文献
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Floquet N Durand P Maigret B Badet B Badet-Denisot MA Perahia D 《Journal of molecular biology》2009,385(2):653-2352
The large protein motions of the bacterial enzyme glucosamine-6-phosphate synthase have been addressed using full atom normal modes analysis for the empty, the glucose-6-phosphate and the glucose-6-phosphate + glutamate bound proteins. The approach that was used involving energy minimizations along the normal modes coordinates identified functional motions of the protein, some of which were characterized earlier by X-ray diffraction studies. This method made it possible for the first time to highlight significant energy differences according to whether none, only one or both of the active sites of the protein were occupied. Our data favoured a specific motion of the glutamine binding domain following the fixation of fructose-6-phosphate and suggested a rigidified structure with both sites occupied. Here, we show that most of the collective large amplitude motions of glucosamine-6-phosphate synthase that are modulated by ligand binding are crucial for the enzyme catalytic cycle, as they strongly modify the geometry of both the ammonia channel and the C-tail, demonstrating their role in ammonia transfer and ligand binding. 相似文献
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Mark E. Polhemus Shon A. Remich Bernhards R. Ogutu John N. Waitumbi Lucas Otieno Stella Apollo James F. Cummings Kent E. Kester Christian F. Ockenhouse Ann Stewart Opokua Ofori-Anyinam Isabelle Ramboer Conor P. Cahill Marc Lievens Marie-Claude Dubois Marie-Ange Demoitie Amanda Leach Joe Cohen W. Ripley Ballou D. Gray Heppner Jr. 《PloS one》2009,4(7)