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41.
Zhan Y Brown LE Deliyannis G Seah S Wijburg OL Price J Strugnell RA O'Connell PJ Lew AM 《Immunologic research》2004,30(1):1-14
The most common models of CD4 T-cell deficiency are mice exogenously injected with anti-CD4 antibody (Ab), CD4 knockout (CD4−/−) and major histocompatibility complex (MHC) class II knockout (class II−/−) mice. We recently described the anti-CD4 Ab transgenic mouse (GK) as an improved CD4 cell-deficient model. This review compares
this new GK mouse model with the widely available class II−/− and CD4−/− mice, when exposed to complex antigens (foreign grafts and during bacterial or viral infection). We highlight here the cytometric
and functional differences (including Ab isotype, viral or bacterial clearance, and graft survival) among these CD4 cell-deficient
models. For example, whereas grafts are generally rejected in class II−/− and CD4−/− mice as quickly as in wild-type mice, they survive longer in GK mice. Also, CD4−/− mice produce IgG against both simple model and complex antigens, but class II−/− and GK mice produce small amounts of IgG2a against complex antigens but not simple model antigens. These differences harbinger
the caveats in the use of these various mice. 相似文献
42.
Can energy drinks reduce the depressor effect of ethanol? An experimental study in mice 总被引:3,自引:0,他引:3
Ferreira SE Hartmann Quadros IM Trindade AA Takahashi S Koyama RG Souza-Formigoni ML 《Physiology & behavior》2004,82(5):841-847
Although the popularization of the combined use of alcoholic beverages and energy drinks (ED) containing caffeine, taurine and other substances has increased, there are no controlled experimental studies on the effects of ED alone or combined with ethanol. This work aimed at evaluating the effects of different doses of ED combined or not with ethanol, on the locomotor activity of Swiss mice. The administration of 3.57, 10.71 or 17.86 ml/kg of ED alone increased the locomotor activity of the animals in relation to a control group. Low doses of ethanol (0.5, 1.0 and 1.5 g/kg) alone or in combination with 10.71 ml/kg of ED did not affect their locomotor activity. However, the reduction of activity observed after 2.5 g/kg of ethanol was antagonized by 10.71 ml/kg of ED. Further studies on the mechanisms of this interaction are still needed. 相似文献
43.
Raymond E Biagini Barbara A MacKenzie Deborah L Sammons Jerome P Smith Edward F Krieg Shirley A Robertson Robert G Hamilton 《Annals of allergy, asthma & immunology》2006,97(2):196-202
BACKGROUND: In the absence of a US Food and Drug Administration (FDA)-cleared latex skin testing reagent, in vitro tests remain important for the diagnosis of latex allergy. OBJECTIVE: To evaluate the performance characteristics of IMMULITE 2000 3gAllergy (Immulite), a third-generation, FDA-cleared, continuous random-access immunoanalyzer, for the quantification of latex specific IgE. METHODS: Stored serum samples (N = 201) from patients classified as having positive or negative latex puncture skin test results were measured for latex specific IgE levels using Immulite, and these data were compared with historical results from 3 second-generation, FDA-cleared IgE antilatex assays (AlaSTAT [Ala], AutoCAP [CAP], and HY*TEC enzyme immunoassay [HT]). RESULTS: The diagnostic performances of the CAP, Ala, and Immulite assays (> or = 0.35 kU/L cutoff value) were equivalent in sensitivity and specificity (P > .05). The HT assay (> or = 0.05 kU/L cutoff value) was more sensitive and less specific (P < .05). Immulite (> or = 0.10 kU/L cutoff value) had greater sensitivity than Ala and CAP and greater specificity than HT (P < .05 for both). Diagnostic efficiency was greater for Immulite than for CAP, Ala, and HT (P < .05). CONCLUSIONS: The Immulite system is superior in diagnostic performance, especially at the 0.10 kU/L or greater cutoff level, for the diagnosis of latex allergy compared with older, second-generation assays. Immulite still misclassifies 15.5% of puncture skin test-positive individuals as negative for latex specific IgE. Compared with second-generation assays, Immulite represents a technological advance, with enhanced speed and less operator intervention. 相似文献
44.
45.
Reading Julian P.; Huffman John L.; Wu Joy C.; Palmer Frances T.; Harton Gary L.; Sisson Michael E.; Keyvanfar Keyvan; Gresinger Thomas H.; Cochrane William J.; Fallon Lee A.; Menapace-Drew Gianna F.; Cummings Emilie A.; Jones Shirley L.; Black Susan H.; Schulman Joseph D.; Levinson Gene 《Molecular human reproduction》1995,1(7):362-367
The discovery of nucleated erythrocytes in maternal circulationprovides a potential source for non-invasive prenatal diagnosis.We have evaluated the use of a three-stage procedure to determinethe number of cells that are of fetal rather than maternal origin.First, monoclonal antibodies specific for CD45 and CD14 wereused in conjunction with a magnetic (MACS) column to depleteunwanted leukocytes from maternal blood. This was followed bya positive MACS enrichment for nucleated erythrocytes, usingan anti-CD71 (transferrin receptor) monoclonal antibody. Todiscriminate between fetal nucleated erythrocytes and thoseof maternal origin, enriched fractions were simultaneously stainedwith an anti-fetal haemoglobin (HbF) antibody and hybridizedwith probes specific for X and Y chromosomes. Samples were thensubjected to blind analysis along with negative control samplesfrom non-pregnant volunteers. Using this dual analysis, we wereable to determine that less than one nucleated erythrocyte perml of maternal blood was of fetal origin. Small numbers of thesefetal cells were found in 87.5% of pregnancies, ranging from6 to 35 weeks gestational age. Comparison of HbF and X/Y probedata also suggests that the fetal cells are less suitable forfluorescence in-situ hybridization (FISH) analysis than similarpreparations from other sources. cell separation methods/fluorescence in-situ hybridization/hereditary diseases/polymerase chain reaction/pregnancy 相似文献
46.
Shirley L. Buchanan Richard H. Thompson Brian L. Maxwell D. A. Powell 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1994,100(3):469-483
The different cytoarchitectonic regions of the medial prefrontal cortex (mPFC) have recently been shown to play divergent
roles in associative learning in rabbits. To determine if these subareas of the mPFC, including areas 24 (anterior cingulate
cortex), 25 (infralimbic cortex), and 32 (prelimbic cortex) have differential efferent connections with other cortical and
subcortical areas in the rabbit, anterograde and retrograde tracing experiments were performed using thePhaseolus vulgaris leukoagglutinin (PHA-L), and horseradish peroxidase (HRP) techniques. All three areas showed local dorsal-ventral projections
into each of the other areas, and a contralateral projection to the homologous area on the other side of the brain. All three
also revealed a trajectory through the striatum, resulting in heavy innervation of the caudate nucleus, the claustrum, and
a lighter projection to the agranular insular cortex. The thalamic projections of areas 24 and 32 were similar, but not identical,
with projections to the mediodorsal nucleus (MD) and all of the midline nuclei. However, the primary thalamic projections
from area 25 were to the intralaminar and midline nuclei. All three areas also projected to the ventromedial and to a lesser
extent to the ventral posterior thalamic nuclei. Projections were also observed in the lateral hypothalamus, in an area just
lateral to the descending limb of the fornix. Amygdala projections from areas 32 and 24 were primarily to the lateral, basolateral
and basomedial nuclei, but area 25 also projected to the central nucleus. All three areas also showed projections to the midbrain
periaqueductal central gray, median raphe nucleus, ventral tegmental area, substantia nigra, locus coeruleus and pontine nuclei.
However, only areas 24 and the more dorsal portions of area 32 projected to the superior colliculus. Area 25 and the ventral
portions of area 32 also showed a bilateral projection to the parabrachial nuclei and dorsal and ventral medulla. The dorsal
portions of area 32, and all of area 24 were, however, devoid of these projections. It is suggested that these differential
projections are responsible for the diverse roles that the cytoarchitectonic subfields of the mPFC have been demonstrated
to play in associative learning. 相似文献
47.
Mammalian transforming growth factor beta1 activated after ingestion by Anopheles stephensi modulates mosquito immunity
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Luckhart S Crampton AL Zamora R Lieber MJ Dos Santos PC Peterson TM Emmith N Lim J Wink DA Vodovotz Y 《Infection and immunity》2003,71(6):3000-3009
During the process of bloodfeeding by Anopheles stephensi, mammalian latent transforming growth factor beta1 (TGF-beta1) is ingested and activated rapidly in the mosquito midgut. Activation may involve heme and nitric oxide (NO), agents released in the midgut during blood digestion and catalysis of L-arginine oxidation by A. stephensi NO synthase (AsNOS). Active TGF-beta1 persists in the mosquito midgut to extended times postingestion and is recognized by mosquito cells as a cytokine. In a manner analogous to the regulation of vertebrate inducible NO synthase and malaria parasite (Plasmodium) infection in mammals by TGF-beta1, TGF-beta1 regulates AsNOS expression and Plasmodium development in A. stephensi. Together, these observations indicate that, through conserved immunological cross talk, mammalian and mosquito immune systems interface with each other to influence the cycle of Plasmodium development. 相似文献
48.
Eimeria necatrix: selection and characteristics of a precocious (and attenuated) line 总被引:2,自引:0,他引:2
A line of Eimeria necatrix with an abbreviated life cycle (i.e. a "precocious" line) was derived from the Houghton laboratory strain by repeated passage of the oocysts which were the first to be recovered from infections in chickens. The precocious line had a reproductive potential much lower than that of its parent strain and it was significantly less pathogenic. Its immunogenicity was, however, substantially retained. Selection for precocious development was accompanied by changes in the endogenous development of the parasite with an attendant reduction in its prepatent time. 相似文献
49.
Individual specific antigenic rubella virus (RV) structural proteins are required for accurate serological diagnosis of acute and congenital rubella infections as well as rubella immune status. The RV envelope glycoprotein E1 is the major target antigen and plays an important role in viral-specific immune responses. The native virion is difficult to produce in large quantities and the protein subunits are also difficult to isolate without loss of antigenicity. The production of a soluble RV E1 (designated E1ΔTm) using the baculovirus-insect cell expression system is described. In contrast to wild-type RV E1, the genetically engineered E1ΔTm protein lacks a transmembrane anchor. It behaved as a secretory protein and was secreted abundantly from insect cells. Pulse-chase studies were used to examine the synthesis, glycosylation, and secretion of E1ΔTm by the insect cells. The secreted E1ΔTm protein was purified from serum-free medium by onestep immunochromatography. The purified E1ΔTm protein retained full antigenicity and may be a convenient source of E1 protein for use in diagnostic assay and rubella vaccine development. 相似文献
50.
Robert H. Carlson Chris Gabel Shirley Chan Robert H. Austin 《Biomedical microdevices》1998,1(1):39-47
We demonstrate a novel activation behavior of human leucocyte adhesion under physiological flow conditions in a microfabricated silicon array of channels with length scales similar to those of human capillaries. Vital nuclei stains and cell specific, flourochrome labeled antibodies reveal that the equilibrium distribution of stuck cells in the arrays displays a strong dependence on cell type and nuclear morphology, and there is eventual separation of the two cell types in the array. The distortion of the cells is the same as they experience in vivo and the response of the granulocytes is consistent with a model describing adhesion as a function of the distortion of the cell by its environment; in other words, activated adhesion. We propose that this complex non-random behavior is due to a deformation activated change in the cells relevant to observed in vivo behavior. 相似文献