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1.
Eur Ann Allergy Clin Immunol ; 40(3): 77-83, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19334371

ABSTRACT

BACKGROUND: The natural history of respiratory allergy is commonly characterized by a worsening of symptom severity, frequent comorbidity of rhinitis and asthma, and polysensitization to aeroallergens. The polysensitization phenomenon starts since childhood and is rare to find monosensitized adult patients. However, there are few studies investigating the characteristics of polysensitized patients. METHODS: This study was performed on a large cohort of patients with allergic rhinitis (assessed by ARIA criteria) and/or mild to moderate asthma (assessed by GINA). The kind and the number of sensitizations, their patterns, and the relation with quality of life (QoL) measured by the Juniper's RQLQ guestionnaire, were evaluated. RESULTS: Globally 418 patients (50.2% males, 49.8% females, mean age 26.4 years, range 3.5-65 years, 64 smokers, 371 non-smokers) were enrolled: 220 had allergic rhinitis alone, and 198 allergic rhinitis and asthma. The mean number ofsensitizations was 2.6. Three hundred-five patients (73%) had persistent rhinitis (PER), 220 of them with moderate-severe form. There was no significant derence in rate of rhinitis and asthma in monosensitized or polysensitized patients. Most patients were sensitized to pollens, whereas only 24.2% of them were sensitized to perennial allergens. Polysensitization was significantly associated with some issues of QoL, confirming previous findings, but not with number ofsensitizations. CONCLUSIONS: This study provides data confirming for poly-sensitized patients the relevance of ARIA classification of AR. PER is the most common form of AR in this cohort, symptoms are frequently moderate-severe, and asthma is present in about the half of patients with AR.


Subject(s)
Allergens/adverse effects , Adolescent , Adult , Age Factors , Aged , Animals , Anti-Allergic Agents/therapeutic use , Antigens, Plant/adverse effects , Asthma/drug therapy , Asthma/epidemiology , Asthma/etiology , Cats , Child , Child, Preschool , Cohort Studies , Dogs , Female , Fungi , Humans , Immunization , Italy/epidemiology , Male , Middle Aged , Pollen/adverse effects , Prospective Studies , Pyroglyphidae , Quality of Life , Rhinitis, Allergic, Perennial/drug therapy , Rhinitis, Allergic, Perennial/epidemiology , Rhinitis, Allergic, Perennial/etiology , Rhinitis, Allergic, Seasonal/drug therapy , Rhinitis, Allergic, Seasonal/epidemiology , Rhinitis, Allergic, Seasonal/etiology , Skin Tests , Smoking/epidemiology , Young Adult
2.
Cell Mol Biol (Noisy-le-grand) ; 49(2): 263-75, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12887107

ABSTRACT

In mammals, certain heat shock proteins (hsps) participate in specialized responses to stressors associated with pathogens or tumors, and as such, act as agents of immune surveillance interacting with both innate and adaptive immunity. We are investigating the conservation of this role throughout the class of vertebrates. We have shown that in Xenopus as in mammals, gp96, the major resident of the endoplasmic reticulum, generates MHC-restricted thymus-dependent immunity in vivo and CR in vitro against minor histocompatibility (H) antigens. By as yet unclear mechanisms that may involve classical MHC-unrestricted cytotoxic CD8+ T cells, gp96 also elicits peptide-specific responses against MHC-class I-negative tumors in adult frogs that may involve cytotoxic NK, MHC-unrestricted CD8+ T and NK/T cells. In naturally MHC class I-deficient but immunocompetent Xenopus larvae, gp96 also generates an innate type of anti-tumor response that is independent of chaperoned peptides. Finally, in a subset of Xenopus sIgM+ B cells, a substantial fraction of gp96 is directed to the cell surface by an active process that is upregulated by bacterial stimulation. This may allow gp96 to access the extracellular compartment without necrosis. Given the dual abilities of gp96 to chaperone antigenic peptides and to modulate innate immune responses, we propose that stimulated B cells that are up-regulating surface gp96 can directly interact with antigen presenting cells (APC) and/or T helper (Th) cells to trigger or amplify immune responses.


Subject(s)
Adjuvants, Immunologic , Antigens, Neoplasm/immunology , Biological Evolution , Animals , Antigens, Neoplasm/metabolism , Peptides/metabolism , Phylogeny , Protein Binding , Xenopus
3.
Physiol Biochem Zool ; 72(3): 255-64, 1999.
Article in English | MEDLINE | ID: mdl-10222320

ABSTRACT

The biochemical mechanisms by which hibernators cool as they enter torpor are not fully understood. In order to examine whether rates of substrate oxidation vary as a function of hibernation, liver mitochondria were isolated from telemetered ground squirrels (Spermophilus lateralis) in five phases of their annual hibernation cycle: summer active, and torpid, interbout aroused, entrance, and arousing hibernators. Rates of state 3 and state 4 respiration were measured in vitro at 25 degrees C. Relative to mitochondria from summer-active animals, rates of state 3 respiration were significantly depressed in mitochondria from torpid animals yet fully restored during interbout arousals. These findings indicate that a depression of ADP-dependent respiration in liver mitochondria occurs during torpor and is reversed during the interbout arousals to euthermia. Because this inhibition was determined to be temporally independent of entrance and arousal, it is unlikely that active suppression of state 3 respiration causes entrance into torpor by facilitating metabolic depression. In contrast to the observed depression of state 3 respiration in torpid animals, state 4 respiration did not differ significantly among any of the five groups, suggesting that alterations in proton leak are not contributing appreciably to downregulation of respiration in hibernation.


Subject(s)
Hibernation/physiology , Oxygen Consumption/physiology , Sciuridae/physiology , Animals , Liver/physiology , Mitochondria/physiology , Respiration
4.
J Comp Physiol B ; 167(4): 256-63, 1997 May.
Article in English | MEDLINE | ID: mdl-9203367

ABSTRACT

The effect of exposure to low temperatures (5 degrees C) on lymphocyte proliferation, leukocyte populations, and serum complement levels was examined in the northern leopard frog, Rana pipiens. Proliferation of T lymphocytes in response to phytohemagglutinin stimulation was significantly decreased in frogs kept for 2, 3, and 5 months at 5 degrees C compared to that of animals kept at 22 degrees C. A significant increase in the average percentage of neutrophils and a decrease in the mean percentage of eosinophils was observed in the blood of frogs held for 5 months in the cold compared to animals held at 22 degrees C for the same length of time. Mean serum complement activity after 1 month at 5 degrees C was significantly reduced in comparison to animals held at 22 degrees C and was not detectable after 5 months in the cold. Recovery of complement levels at room temperature (22 degrees C) was also examined after cold exposure. Complement levels were significantly higher than controls (at 22 degrees C) in frogs returned to 22 degrees C for 7 and 14 days after 5 months in the cold. After frogs were held at 5 degrees C for 1 month, serum complement levels increased significantly within 2 days after returning to 22 degrees C and continued to rise 5 and 9 days after warming. Injections with Aeromonas hydrophila following a 5-week exposure to 5 degrees C failed to cause death or observable symptoms of disease in frogs that were returned to 22 degrees C.


Subject(s)
Adaptation, Physiological/physiology , Cold Temperature/adverse effects , Complement System Proteins/analysis , Leukocytes/physiology , Lymphocyte Activation/physiology , Rana pipiens/immunology , Animals , Cell Division/physiology , Leukocyte Count/veterinary , Leukocytes/classification , Lymphocyte Activation/immunology , Phytohemagglutinins/pharmacology , Temperature , Time Factors
5.
Aviat Space Environ Med ; 61(2): 162-4, 1990 Feb.
Article in English | MEDLINE | ID: mdl-2178600

ABSTRACT

Aircrews operating at high G forces and altitudes may be exposed to both physiological and physical stresses capable of inducing brain hypoxia. A potential therapeutic tool for the treatment of flight personnel, monosialoganglioside (GM1) has been found to reduce deficits and enhance repair following CNS injury. A survey of experimental evidence concerning the effects of GM1 in the acute phase of CNS injury supports its proposed application for aerospace medicine.


Subject(s)
Brain Damage, Chronic/therapy , G(M1) Ganglioside/administration & dosage , Hypoxia, Brain/therapy , Animals , Gravitation , Humans , Nerve Regeneration/drug effects , Space Flight
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