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1.
Eur J Neurol ; 25(6): 833-840, 2018 06.
Article in English | MEDLINE | ID: mdl-29489040

ABSTRACT

BACKGROUND AND PURPOSE: Ataxia-telangiectasia (A-T) is a rare neurodegenerative disease, due to A-T mutated (ATM) gene mutations, which typically presents with signs of progressive neurological dysfunction, cerebellar ataxia and uncoordinated movements. A-T severely affects patients' quality of life. Successful treatment options are still not available. The aim of this multicenter study, performed with a blind evaluation procedure, was to define the minimal effective dosage of oral betamethasone, thus preventing the occurrence of side effects. METHODS: Nine A-T patients were enrolled to receive betamethasone at increasing dosages of 0.001, 0.005 and 0.01 mg/kg/day. Neurological assessment and the evaluation of quality of life were performed through the Scale for the Assessment and Rating of Ataxia and the Italian version of the Childhood Health Assessment Questionnaire (CHAQ) at each time-point. The drug safety profile was evaluated. Patients were categorized as responders, partial responders and non-responders. RESULTS: Four of nine patients had a benefit at a dose of 0.005 mg/kg/day of oral betamethasone. Using the higher dosage, only one additional patient had a positive response. Conversely, a daily dose of 0.001 mg/kg was ineffective. A correlation between the serum adrenocorticotropic hormone levels and the clinical response was observed. Five of 30 CHAQ items improved in four patients. CONCLUSIONS: These data suggest that a short-term betamethasone oral treatment, at a daily dosage of 0.005 mg/kg, is effective in some patients. Pre-existing risk factors for side effects should be taken into account before therapy.


Subject(s)
Ataxia Telangiectasia/drug therapy , Betamethasone/administration & dosage , Glucocorticoids/administration & dosage , Adolescent , Betamethasone/therapeutic use , Child , Child, Preschool , Dose-Response Relationship, Drug , Female , Glucocorticoids/therapeutic use , Humans , Male , Phenotype , Quality of Life , Treatment Outcome , Young Adult
2.
Genes Immun ; 16(7): 481-7, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26335810

ABSTRACT

Kawasaki disease (KD) is a pediatric acute multisystemic vasculitis complicated by development of coronary artery lesions. The breakthrough theory on KD etiopathogenesis points to pathogens/environmental factors triggered by northeastern wind coming from China. Natural Killer cells and T lymphocytes express the inhibitory/activating Killer Immunoglobulin-like Receptors (KIR) to elicit an immune response against pathogens by binding to human leukocyte antigens (HLA) class I epitopes. We first report on the role of KIR/HLA genetic epistasis in a sample of 100 Italian KD children. We genotyped KIR, HLA-A, HLA-B and HLA-C polymorphisms, and compared KD data with those from 270 Italian healthy donors. The HLA-A*11 ligand for KIR2DS2/2DS4/3DL2 was a KD susceptibility marker by itself (odds ratio (OR)=3.85, confidence interval (CI)=1.55-9.53, P=0.004). Although no epistasis between HLA-A*11 and KIR2DS2/S4 emerged, HLA-A*11 also engages KIR3DL2, a framework gene encoding for a pathogen sensor of CpG-oligodeoxynucleotides (CpG-ODN), and KD blood mononuclear cells are actually prone to pathogen CpG-ODN activation in the acute phase. Moreover, carriers of KIR2DS2/HLA-C1 and KIR2DL2/HLA-C1 were more frequent among KD, in keeping with data demonstrating the involvement of these HLA/KIR couples in autoimmune endothelial damage. The highest KD risk factor was observed among carriers of KIR2DL2 and two or more HLA ligands (OR=10.24, CI=1.87-56.28; P=0.007).


Subject(s)
HLA Antigens/genetics , HLA Antigens/immunology , Mucocutaneous Lymph Node Syndrome/genetics , Mucocutaneous Lymph Node Syndrome/immunology , Receptors, KIR/genetics , Receptors, KIR/immunology , Case-Control Studies , Child , Child, Preschool , Disease Susceptibility/immunology , Epistasis, Genetic , Female , Gene Frequency , HLA-A11 Antigen/genetics , HLA-B Antigens/genetics , HLA-C Antigens/genetics , Histocompatibility Antigens Class II/genetics , Histocompatibility Antigens Class II/immunology , Humans , Immunoglobulins/genetics , Immunoglobulins/immunology , Male , Polymorphism, Genetic
3.
Talanta ; 120: 283-8, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24468371

ABSTRACT

The paper describes the characterization of polycyclic aromatic hydrocarbons (PAHs) in atmospheric aerosol samples using Gas Chromatography-Mass Spectrometry analysis. A data handling of GC/MS signals based on Experimental Autocovariance Function (EACVF) is described in order to directly characterize PAHs with a simple and reliable method suitable for processing large batches of samples. The method was successfully applied to 42 aerosol samples collected in different seasons (summer, fall and winter) in two locations in Northern Italy: Milan, a large urban area, and Oasi Le Bine, a rural site. The reliability of the EACVF results was verified by comparison with the values computed with the conventional GC/MS signal treatment and the data of independent studies. Two main emission sources were identified and described by PAH concentration profiles: the road traffic source (TR), characterized by high contributions of FLNT, PYR and CHR, and the residential combustion (COMB) mainly containing pyrogenic high molecular weight PAHs, i.e., CHR, BaP, BeP, BbF and BkF. In addition, some PAH diagnostic ratios were directly computed for the EACVF plot, to distinguish between traffic and combustion dominated emissions, i.e. the ratios CHR/BaP, PYR/BaP and PYR/BeP.


Subject(s)
Aerosols/analysis , Air Pollutants/analysis , Environmental Monitoring/methods , Gas Chromatography-Mass Spectrometry/methods , Polycyclic Aromatic Hydrocarbons/analysis , Italy , Reproducibility of Results
4.
J Mass Spectrom ; 48(2): 216-26, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23378094

ABSTRACT

Liquid chromatography (LC) combined with tandem mass spectrometry (MS/MS), based on the use of a hybrid quadrupole-time-of-flight mass analyzer, was used to investigate the reactivity of nine fungicides in free chlorine-containing water samples. Three of the selected compounds (fenhexamid, FEN; pyrimethanil, PYR; and cyprodinil, CYP) displayed a poor stability in presence of moderate chlorine levels; thus, the effects of different parameters on their half-lives (t(1/2)) were evaluated. Sample pH, bromide traces, and the water matrix affected their relative stabilities. Despite such variations, the three fungicides are degraded at significant rates not only in ultrapure, but also in surface water spiked with chlorine levels up to 2 µg ml(-1), and when mixed with chlorinated tap water, generating several transformation products (TPs). The time-course of precursor species and their TPs was followed in the LC-MS mode, using the information contained in accurate, full scan mass spectra (MS) to propose the empirical formulae of TPs. Thereafter, their ion product scan (MS/MS) spectra were considered to set their chemical structures; allowing, in some cases, to distinguish between isomeric TPs. The reaction pathway of FEN, the less stable fungicide, involved just an electrophilic substitution of hydrogen per chlorine, or bromine, and cleavage of the molecule to render an amide. PYR and CYP shared common reaction routes consisting of halogenation, hydroxylation, and condensation processes leading to complex mixtures of TPs, which were relatively stable to further transformations.

5.
J Biol Regul Homeost Agents ; 27(4): 935-46, 2013.
Article in English | MEDLINE | ID: mdl-24382174

ABSTRACT

Primary immunodeficiencies (PIDs) are rare diseases characterized by an increased susceptibility to infections. Early diagnosis and appropriate treatment are critical for reducing morbidity and mortality. Based on available data, the efficacy of antibiotic administration for the prophylaxis of infections remains uncertain, and recommendations supporting this practice are poor. The use of antimicrobial prophylaxis is mainly based on single institution-specific experience without controlled measurements of patient safety and quality health outcomes. To address this issue an Italian Network on Primary Immunodeficiencies (IPINet) has been set up in 1999 within the Italian Association of Pediatric Hematology and Oncology (AIEOP) to increase the awareness of these disorders among physicians. Further, diagnostic and treatment guideline recommendations have been established to standardize the best clinical assistance to all patients, including antibiotic prophylaxis, and for a national epidemiologic monitoring of PIDs. The aim of this review is not only to give a scientific update on the use of antimicrobial prophylaxis in selected congenital immunological disorders but also to draw a picture of this practice in the context of the Italian Primary Immunodeficiency Network (IPINet). Controlled multicenter studies are necessary to establish if, when and how you should start an efficacious antimicrobial prophylaxis.


Subject(s)
Antibiotic Prophylaxis , Immunologic Deficiency Syndromes/complications , Common Variable Immunodeficiency/complications , DiGeorge Syndrome/complications , Granulomatous Disease, Chronic/complications , Humans , IgA Deficiency/complications , X-Linked Combined Immunodeficiency Diseases/complications
6.
Anal Bioanal Chem ; 399(6): 2257-65, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21221545

ABSTRACT

A multi-residual method is described for the simultaneous determination of 23 personal care products (PCPs), which display a wide range of physicochemical properties, present at trace levels in water samples. A one-step procedure was developed based on solid-phase microextraction (SPME) coupled with GC-MS analysis. A chemometric approach consisting of an experimental design (design of experiments) was applied to systematically investigate how four operating parameters--extraction temperature and time and desorption temperature and time--affect extraction recovery of PCPs in water. The optimum SPME procedure operating conditions, those yielding the highest extraction recovery for all the compounds, were determined; they correspond to an extraction time of 90 min and temperature of 80 °C and a desorption time of 11 min and temperature of 260 °C. Under these optimized conditions, the SPME procedure shows good analytical performance characterized by high reproducibility (RSD% intra-day accuracy varying in the 0.01-1.3% range) as well as good linearity and low detection limits (LODs lower than 2 ppb for most of the investigated PCPs).


Subject(s)
Cosmetics/isolation & purification , Solid Phase Microextraction/methods , Water Pollutants, Chemical/isolation & purification , Cosmetics/analysis , Gas Chromatography-Mass Spectrometry , Water Pollutants, Chemical/analysis
7.
Environ Sci Technol ; 44(11): 4232-40, 2010 Jun 01.
Article in English | MEDLINE | ID: mdl-20450188

ABSTRACT

The paper describes the characterization of n-alkane homologous series present in PM samples performed by gas chromatography-mass spectrometry analysis. The PM samples were collected in three locations in northern Italy: Milan, a large urban area, Oasi Bine, a rural site far from big city centers, and Alpe San Colombano, a remote, high altitude site in the Alps. They represent different particle sizes (PM(1), PM(2.5), PM(10)) and seasons (summer, fall, and winter). The analyzed samples were characterized in terms of PM total mass, total concentration of C(20)-C(32) n-alkanes and carbon preference index, CPI, to quantify the relative abundance of odd versus even n-alkanes. As alternative to the conventional method based on peak integration, a chemometric approach based on autocovariance function (EACVF) computation was found reliable to characterize the homologous series. In particular two parameters have proven useful chemical markers for tracking the biogenic and anthropogenic origins of n-alkanes: CPI(EACVF) and series %, estimating the % n-alkanes abundance relative to total alkane concentration. The investigated samples display a large variation in the n-alkanes relative abundance: the lowest values (series % = 1-14%) were found in summer and the highest (series % = 24-48%) in winter. In addition, a considerable seasonal variation of CPI(EACVF) values can be identified for all the sampling sites: the CPI(EACVF) values are close to 1 (CPI(EACVF) = 0.8-1.2) in the cold seasons, revealing a strong contribution from anthropogenic emissions, while spreader values (CPI(EACVF) = 0.9-3) were found in the warm season, that is, reflecting a variable contribution from biogenic sources in combination with anthropogenic emissions.


Subject(s)
Aerosols/chemistry , Alkanes/analysis , Gas Chromatography-Mass Spectrometry/methods , Italy , Particle Size
8.
J Chromatogr A ; 1217(7): 1126-33, 2010 Feb 12.
Article in English | MEDLINE | ID: mdl-19815225

ABSTRACT

The work compares two GC-MS methods for enantioselective separation of amino acids as suitable candidate for stereochemical analysis of chiral amino acids on board spacecrafts in space exploration missions of solar system body environments. Different derivatization reagents are used: a mixture of alkyl chloroformate-alcohol-pyridine to obtain the alkyl alkoxy carbonyl esters and a mixture of perfluorinated alcohols and anhydrides to form perfluoroacyl perfluoroalkyl esters. 20 proteinogenic amino acids were derivatized with the two procedures and submitted to GC-MS analysis on a Chirasil-l-Val stationary phase. The results were then compared in terms of the enantiomeric separation achieved and intensity of MS response. The combination of methyl chloroformate (MCF) and heptafluoro-1-butanol (HFB) allows separation of 14 enantiomeric pairs, five of which display a resolution (R(s)>or=1.2) supposed to be sufficient to quantify the enantiomeric excess. Three mixtures of trifluoroacetic (TFAA) and heptafluorobutyric (HFBA) anhydrides were combined with the corresponding perfluorinated alcohols - TFE (2,2,2-trifluoro-1-ethanol) and HFB (2,2,3,3,4,4,4-heptafluoro-1-butanol) - to give three different reagents (TFAA-TFE, TFAA-HFB, HFBA-HFB): the derivatives obtained show separation of the same number of proteinogenic amino acids (14 of 20) at a temperature lower than column bleeding limit (200 degrees C) and 8 of them give a separation with R(s)>or=1.2. Linearity study and limit of detection (X(LOD)) computation show that both methods are suitable for quantitative determination of several amino acid diastereomers at trace level (X(LOD) approximately 0.5nmol as derivatized quantity). Both the procedures were coupled with automatic data handling to increase their suitability for space analysis: the simplified data treatment is especially helpful to handle the low quality data recovered from space experiments and labor and time are saved, as imposed by the space experiments requiring a rapid delivery of the results. To achieve this aim, a chemometric approach based on the computation of the Autocovariance Function (ACVF) was applied to extract information on the enantiomeric pairs present in the sample and the enantioseparation achieved on the chiral column.


Subject(s)
Amino Acids/chemistry , Gas Chromatography-Mass Spectrometry/methods , Signal Processing, Computer-Assisted , Alcohols/chemistry , Biomarkers/chemistry , Formates/chemistry , Linear Models , Sensitivity and Specificity , Stereoisomerism , Temperature
9.
Clin Immunol ; 129(3): 448-54, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18835223

ABSTRACT

Dominant-negative mutations in STAT-3 have recently been found in the majority of patients with sporadic or autosomal-dominant hyper IgE syndrome (HIES). Since STAT-3 plays a role in B cell development and differentiation, we analyzed memory B cells in 20 patients with HIES, 17 of which had STAT-3 mutations. All but four patients had reduced non-switched and/or class-switched memory B cells. No reduction in these B cell populations was found in 16 atopic dermatitis patients with IgE levels above 1000 KU/L. There was no correlation between the reduction of memory B cells and the ability to produce specific antibodies. Moreover, there was no correlation between the percentage of memory B cells and the infection history. Analysis of memory B cells can be useful in distinguishing patients with suspected HIES from patients with atopic disease, but probably fails to identify patients who are at high risk of infection.


Subject(s)
B-Lymphocytes/immunology , Immunologic Memory/immunology , Job Syndrome/immunology , Adolescent , Adult , Antibodies, Viral/blood , Antibody Formation , B-Lymphocytes/pathology , Child , Cohort Studies , DNA/chemistry , DNA/genetics , Dermatitis, Atopic/genetics , Dermatitis, Atopic/immunology , Dermatitis, Atopic/pathology , Enzyme-Linked Immunosorbent Assay , Female , Flow Cytometry , Genotype , Humans , Immunoglobulin E/immunology , Immunoglobulin E/metabolism , Immunologic Memory/genetics , Job Syndrome/genetics , Job Syndrome/pathology , Male , Middle Aged , Mutation , STAT3 Transcription Factor/genetics , STAT3 Transcription Factor/immunology , Young Adult
10.
Int J Immunopathol Pharmacol ; 21(2): 343-52, 2008.
Article in English | MEDLINE | ID: mdl-18547478

ABSTRACT

Transient hypogammaglobulinemia of infancy (THI) is a heterogeneous disorder characterized by reduced serum IgG levels in early infancy. A putative diagnosis is initially made after exclusion of other causes of hypogammaglobulinemia while a definitive diagnosis of THI can only be made a posteriori in patients with normalization of IgG levels. The aim of this study is to characterize clinical and immunological features of children with an initial diagnosis of THI in correlation to natural outcome, and to assess predictive laboratory parameters of clinical evolution for this disorder. We prospectively analysed clinical and immunological characteristics of 77 THI children at initial diagnosis and of 57 patients at follow-up. Memory B cell subsets and in vitro immunoglobulin production were evaluated. Seventy patients (91 percent) showed clinical symptoms. Patients suffered from infections (91 percent), allergies (47 percent) and autoimmune disease (4 percent). During follow-up 41/57 children (72 percent) normalized IgG values, mostly within 24 months of age (p less than 0.001), allowing the diagnosis of THI. The 16 children who did not normalize their IgG levels showed a higher frequency of severe infections and autoimmune disease (p less than 0.01). Moreover, they expressed a reduced frequency of IgM and switched memory B cells (p less than 0.01) and an inability to produce IgG in vitro (p less than 0.02). We conclude that most patients with an initial diagnosis of THI spontaneously recover within 24 months of age and have a benign clinical course, while a subgroup of children with undefined hypogammaglobulinemia share a clinical and immunological profile with other primary immunodeficiencies. Early recognition of children with hypogammaglobulinemia during infancy who are likely to suffer from permanent immunodeficiencies later in life would allow prompt and appropriate laboratory and clinical interventions.


Subject(s)
Agammaglobulinemia/epidemiology , Immunologic Deficiency Syndromes/epidemiology , Aging/immunology , B-Lymphocytes/immunology , Child, Preschool , Disease Progression , Female , Humans , Immunoglobulin A/blood , Immunoglobulin G/blood , Immunoglobulin M/blood , Immunoglobulins/biosynthesis , Immunologic Memory/immunology , Infant , Italy/epidemiology , Male , Prospective Studies , Treatment Outcome
11.
Genes Immun ; 8(4): 325-33, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17410177

ABSTRACT

Autosomal-recessive agammaglobulinemia is a rare and heterogeneous disorder, characterized by early-onset infections, profound hypogammaglobulinemia of all immunoglobulin isotypes and absence of circulating B lymphocytes. To investigate the molecular basis of the disease, 23 patients with early-onset disease and no mutations in Bruton tyrosine kinase, the gene responsible for X-linked agammaglobulinemia, were selected and analyzed by direct sequencing of candidate genes. Two novel mutations in the mu heavy chain (muHC) gene (IGHM) were identified in three patients belonging to two unrelated families. A fourth patient carries a previously described G>A nucleotide substitution at the -1 position of an alternative splice site in IGHM; here, we demonstrate that this mutation is indeed responsible for aberrant splicing. Comparison of bone marrow cytofluorimetric profiles in two patients carrying different mutations in the IGHM gene suggests a genotype-phenotype correlation with the stage at which B-cell development is blocked. Several new single nucleotide polymorphisms (SNPs) both in the muHC and in the lambda5-like/VpreB-coding genes were identified. Two unrelated patients carry compound heterozygous variations in the VpreB1 gene that may be involved in disease ethiology.


Subject(s)
Agammaglobulinemia/genetics , B-Lymphocytes/immunology , Genes, Immunoglobulin , Immunoglobulin Light Chains/genetics , Immunoglobulin mu-Chains/genetics , Membrane Glycoproteins/genetics , Polymorphism, Single Nucleotide , Receptors, Antigen, B-Cell/genetics , Adolescent , Adult , Agammaglobulinaemia Tyrosine Kinase , Agammaglobulinemia/immunology , Child , Child, Preschool , Female , Flow Cytometry , Genes, Recessive , Humans , Immunoglobulin Light Chains, Surrogate , Infant , Italy , Male , Mutation , Polymerase Chain Reaction , Protein-Tyrosine Kinases/genetics , Receptors, Antigen, B-Cell/immunology
12.
J Chromatogr A ; 1150(1-2): 162-72, 2007 May 25.
Article in English | MEDLINE | ID: mdl-17222857

ABSTRACT

This work describes a GC-MS method for enantioselective separation of amino acids. The method is based on a derivatization reaction which employs a mixture of alkyl chloroformate-alcohol-pyridine, as reagents to obtain the N(O,S)-alkyl alkoxy carbonyl esters of amino acids. Various reaction parameters are investigated and optimized to achieve a reproducible derivatization procedure suitable for separation of amino acid enantiomers on Chirasil-L-Val chiral stationary phase. In particular, the following topics are investigated for 20 proteinogenic amino acids: (i) the proper reagent and reaction conditions to obtain the highest derivative yield; (ii) the amino acid reactivity and the MS properties of the obtained derivatives; (iii) the linearity and sensitivity of the analytical method; (iv) the retention behavior of the derivatives and their enantiomeric separation on the Chirasil-L-Val chiral stationary phase. By combining the resolution power of the Chirasil-L-Val column and the high selectivity of the SIM MS detection mode, the described procedure enables the enantiomeric separation and quantification of 16 enantiomeric pairs of amino acids. The procedure is simple and fast and reproducible. It displays a wide linearity range at ppb detection limits for quantitative determinations: these properties make this derivatization method a suitable candidate for amino acid GC-MS analysis on board of the spacecrafts in space exploration missions of solar system body environments.


Subject(s)
Amino Acids/chemistry , Formates/chemistry , Gas Chromatography-Mass Spectrometry/methods , Amino Acids/analysis , Molecular Structure , Reproducibility of Results , Stereoisomerism
13.
Chirality ; 18(4): 279-95, 2006 May 05.
Article in English | MEDLINE | ID: mdl-16534802

ABSTRACT

The target of the in-situ research of optical activity in extraterrestrial samples stimulated an extended investigation of a GC-MS method based on the derivatization of amino acids by using a mixture of perfluorinated alcohols and perfluorinated anhydrides. Amino acids are converted to their N(O,S)-perfluoroacyl perfluoroalkyl esters in a single-step procedure, using different combinations of the derivatization reagents trifluoroacetic anhydride (TFAA)-2,2,2-trifluoro-1-ethanol (TFE), TFAA-2,2,3,3,4,4,4-heptafluoro-1-butanol (HFB), and heptafluorobutyric anhydride (HFBA)-HFB. The derivatives obtained are analyzed using two different chiral columns: Chirasil-L-Val and gamma-cyclodextrin (Rt-gamma-DEXsa) stationary phases which show different and complementary enantiomeric selectivity. The mass spectra of the derivatives are studied, and mass fragmentation patterns are proposed: significant fragment ions can be identified to detect amino acid derivatives. The obtained results are compared in terms of the enantiomeric separation achieved and mass spectrometric response. Linearity studies and the measurement of the limit of detection (LOD) show that the proposed method is suitable for a quantitative determination of enantiomers of several amino acids. The use of the programmed temperature vaporiser (PTV) technique for the injection of the untreated reaction mixture is a promising method for avoiding manual treatment of the sample and decreasing the LOD.


Subject(s)
Amino Acids/analysis , Space Flight , Acylation , Amino Acids/chemistry , Calibration , Esterification , Esters/analysis , Esters/chemistry , Gas Chromatography-Mass Spectrometry , Molecular Structure , Reference Standards , Stereoisomerism , Time Factors , Volatilization
14.
J Chromatogr A ; 1071(1-2): 255-61, 2005 Apr 15.
Article in English | MEDLINE | ID: mdl-15865201

ABSTRACT

Gas chromatography-mass spectrometry (GC-MS) will be used in future space exploration missions, in order to seek organic molecules at the surface of Mars, and especially potential chemical indicators of life. Carboxylic acids are among the most expected organic species at the surface of Mars, and they could be numerous in the analysed samples. For this reason, a chemometric method was applied to support the interpretation of chromatograms of carboxylic acid mixtures. The method is based on AutoCovariance Function (ACVF) in order to extract information on the sample--number and chemical structure of the components--and on separation performance. The procedure was applied to standard samples containing targeted compounds which are among the most expected to be present in the Martian soil: n-alkanoic and benzene dicarboxylic acids. ACVF was computed on the obtained chromatograms and plotted versus retention time: peaks of the ACVF plot can be related to specific molecular structures and are diagnostic for chemical identification of compounds.


Subject(s)
Exobiology , Gas Chromatography-Mass Spectrometry/methods , Mars , Soil/analysis
15.
Arch Dis Child ; 88(12): 1101-5, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14670780

ABSTRACT

AIMS: To prospectively evaluate sinopulmonary disease in 24 patients with primary humoral immunodeficiency (11 with agammaglobulinaemia, nine with isolated IgA deficiency, and two with common variable immunodeficiency) and chronic productive cough, ascertain the usefulness of chest high resolution computed tomography (HRCT) in evaluating the progression of lung disease, and test a therapeutic approach to chronic sinusitis. METHODS: Pulmonary abnormalities were evaluated using lung function tests and HRCT (Bhalla score); chronic sinusitis was diagnosed clinically and confirmed by flexible fibreoptic endoscopy. Sixteen patients entered the three year follow up. RESULTS: Lung function testing revealed an obstruction in four patients; chest HRCT was abnormal in 16. There was a linear relation between the Bhalla score > or =4 and the number of months with cough/year over the previous two years (clinical score), and between the difference in clinical scores during follow up and in the previous two years and the difference in Bhalla score. The pulmonary lesions did not significantly progress over a three year period. Thirteen patients had chronic sinusitis; 6/10 patients followed up were successfully treated with antibiotics plus topical therapy and two with nasal polypoid disease with endoscopic sinus surgery. CONCLUSIONS: In patients with primary humoral immunodeficiency and chronic productive cough, HRCT is very useful in delineating the extent of lung damage. The correlation between Bhalla score and clinical findings and the favourable outcome of the disease suggests that in most patients chest HRCT should not be repeated annually as previously suggested. Medical therapy seems to be effective in many cases of chronic sinusitis.


Subject(s)
Cough/immunology , Immunologic Deficiency Syndromes/immunology , Lung Diseases/immunology , Paranasal Sinuses/immunology , Adolescent , Adult , Agammaglobulinemia/immunology , Antibody Formation/immunology , Child , Child, Preschool , Chronic Disease , Female , Follow-Up Studies , Forced Expiratory Volume/physiology , Humans , Infant , Male , Prospective Studies , Tomography, X-Ray Computed , Vital Capacity/physiology
16.
Neuropediatrics ; 32(5): 250-5, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11748496

ABSTRACT

Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease due to infection with polyomavirus JC (JCV). PML occurs almost exclusively in immunocompromised patients, and although it has increased markedly in relation to AIDS, remains exceptional in children. We present the case of an immunocompromised child with hyperimmunoglobulin E recurrent infection syndrome (HIES) and pathologically-proven PML. HIES is a rare congenital immunodeficiency that to our knowledge has never before been reported in association with neurological complications. Following a recurrence of bronchopneumonia, the child's motor and cognitive functions deteriorated progressively in parallel with alterations on cerebral MRI. The neurological onset coincided with lymphocyte subset changes. PCR for JCV DNA did not detect the virus in CSF, and brain biopsy was required to secure the diagnosis. Antiviral treatment with cidofovir produced no benefit. Autopsy revealed the typical neuropathological findings of PML which were associated with inflammatory eosinophilic infiltrate (a marker of HIES). In accordance with the few pediatric PML cases reported and here reviewed, the child died five months after neurological onset.


Subject(s)
Hypergammaglobulinemia/diagnosis , Immunoglobulin E/blood , Leukoencephalopathy, Progressive Multifocal/diagnosis , Opportunistic Infections/diagnosis , Staphylococcal Infections/diagnosis , Brain/pathology , Child , Encephalitis/diagnosis , Encephalitis/pathology , Fatal Outcome , Humans , Hypergammaglobulinemia/pathology , Leukoencephalopathy, Progressive Multifocal/pathology , Magnetic Resonance Imaging , Male , Oligodendroglia/pathology , Opportunistic Infections/pathology , Recurrence , Staphylococcal Infections/pathology
18.
Cardiologia ; 43(12): 1367-74, 1998 Dec.
Article in Italian | MEDLINE | ID: mdl-9988946

ABSTRACT

We report a prospective study performed over a 9 year period in 96 children with Kawasaki disease (mean age 35 +/- 29 months), 84 of whom < 5 years of age. The male/female ratio was 1.5 (57/39). A total of 38 patients had cardiac involvement, including flattened T waves in the ECG (10 patients), pericardial effusion (6 patients), myocarditis (1 patient), and coronary artery aneurysms (25 patients; frequency of aneurysms: 26%). All patients were evaluated during the acute phase (first month) of the illness. The first echocardiographic examination was performed 15 days (range 4.30 days) from the appearance of fever, and coronary aneurysms were observed in 23 patients; in 2 patients, however, aneurysms appeared later (2 and 6 months). Aneurysms were small (< or = 4.5 mm) in 12, medium (4.5-7 mm) in 11, and large (> 7 mm) in 12 patients. Male sex (p = 0.02), age < 12 months (p = 0.005), ESR (p = 0.001), platelet count (p = 0.009), and pericardial effusion (p = 0.02) were significantly related to the presence of aneurysm. Among females, incidence of aneurysms was significantly higher in infants < 12 months than in older patients (60 vs 6%, p < 0.001). Intravenous immunoglobulin treatment was started early (within 10 days) in 61 patients and late (> 10 days) in 22. Compared to late treatment, early i.v. immunoglobulin treatment was associated with smaller aneurysms and higher regression rate (67 vs 28%, p < 0.05). No difference was observed concerning frequency and number of dilated vessels as related to therapeutical regimens. Total i.v. immunoglobulin dose (2 g/kg) was administered over 1-2 days in 26 patients (scheme I) or over 4-5 days in 58 (scheme II). Frequency of aneurysms was significantly lower in patients treated early (p = 0.02). No myocardial infarctions or deaths occurred at short- or long-term follow-up.


Subject(s)
Cardiovascular Diseases/complications , Mucocutaneous Lymph Node Syndrome/complications , Cardiovascular Diseases/prevention & control , Child, Preschool , Coronary Aneurysm/complications , Coronary Aneurysm/prevention & control , Female , Humans , Infant , Male , Mucocutaneous Lymph Node Syndrome/therapy , Prospective Studies
19.
Eur J Pediatr ; 150(1): 37-9, 1990 Nov.
Article in English | MEDLINE | ID: mdl-2079075

ABSTRACT

The Multitest skin test allows the simultaneous intradermal application of seven standardized recall antigens in a reproducible manner. Response reading is based on a scoring system that distinguishes between normal and diminished delayed hypersensitivity (DH). To determine incidence and size of DH responses for each antigen in relation to age and sex in healthy Italian children, a multicentric study was performed on a representative paediatric population of 491 subjects (285 males and 296 females) aged from 4 months to 16 years. In both sexes DH reactivity as measured by score and number of positive responses increased significantly with age. The incidence of anergy was 8.8% for the whole population and decreased significantly with age in both sexes. Incidence of positive responses was highest for tetanus and diphteria toxoids, intermediate for Candida, Proteus and Streptococcus, and lowest for tuberculin and Trichophyton antigens. There was no significant difference between sexes in the incidence of positive response to each antigen.


Subject(s)
Hypersensitivity, Delayed/diagnosis , Skin Tests/methods , Adolescent , Chi-Square Distribution , Child , Child, Preschool , Female , Humans , Hypersensitivity, Delayed/immunology , Infant , Italy , Male , Reference Values , Regression Analysis
20.
J Pharm Pharmacol ; 42(6): 401-4, 1990 Jun.
Article in English | MEDLINE | ID: mdl-1979619

ABSTRACT

The hypothesis that benzodiazepines interact with their receptors in the CNS via hydrogen bonding mediated by the carbonyl and imine groups has been studied by correlating a physicochemical parameter affected by hydrogen bonds potentially accepted or donated by benzodiazepines with their binding constants to synaptosomal rat brain membranes. The reference physicochemical system chosen was normal phase high-performance liquid chromatography on mu-Bondapack NH2 (propylamine groups chemically bonded to porous silica) eluted with mixtures of n-hexane and 2-propanol. A strong correlation has been found for binding of the implicated groups to the column and to the receptor.


Subject(s)
Receptors, GABA-A/metabolism , 1-Propanol , Animals , Chemical Phenomena , Chemistry, Physical , Chromatography, High Pressure Liquid , Hexanes , Hydrogen Bonding , In Vitro Techniques , Kinetics , Models, Chemical , Rats , Receptors, GABA-A/chemistry , Silicon Dioxide , Solvents , Synaptosomes/metabolism
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