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1.
Allergol Immunopathol (Madr) ; 45(1): 55-62, 2017.
Article in English | MEDLINE | ID: mdl-27480789

ABSTRACT

BACKGROUND: This is a prospective study that assessed pneumococcal antibody levels in PID patients under intravenous immunoglobulin (IVIG) treatment using different brands. METHODS: Twenty-one patients receiving regular IVIG every 28 days were invited to participate: 12 with common variable immunodeficiency, six with X-linked agammaglobulinaemia and three with hyper-IgM syndrome. One blood sample was collected from each patient just prior to IVIG administration at a three-month time interval during one year. A questionnaire was filled in with patient's demographic data and history of infections during the study period. Streptococcus pneumoniae antibodies against six serotypes (1, 5, 6B, 9V, 14 and 19F) were assessed by ELISA both in patients' serum (trough levels) and in IVIG samples. RESULTS: Median total IgG trough serum levels were 7.91g/L (range, 4.59-12.20). All patients had antibody levels above 0.35µg/mL to the six serotypes on all four measurements. However, only 28.6% of patients had pneumococcal antibodies for the six analysed serotypes above 1.3µg/mL on all four evaluations during the one-year period. No correlation was found between IgG trough levels and pneumococcal specific antibodies. Eighteen of the 21 patients (85.7%) had infections at some point during the 12-month follow-up, 62/64 (96.9%) clinically classified in respiratory tract infections, four of which were pneumonia. CONCLUSIONS: Pneumococcal antibodies are present in a high range of concentrations in sera from PID patients and also in IVIG preparations. Even maintaining a recommended IgG trough level, these patients can be susceptible to these bacteria and that may contribute to recurrent respiratory infections.


Subject(s)
Antibodies, Bacterial/blood , Immunoglobulins, Intravenous/therapeutic use , Immunologic Deficiency Syndromes/immunology , Pneumonia, Pneumococcal/immunology , Streptococcus pneumoniae/immunology , Adolescent , Adult , Brazil , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Immunoglobulin G/blood , Immunologic Deficiency Syndromes/therapy , Male , Pneumonia, Pneumococcal/therapy , Prospective Studies , Young Adult
2.
Allergol Immunopathol (Madr) ; 43(3): 272-8, 2015.
Article in English | MEDLINE | ID: mdl-25796303

ABSTRACT

BACKGROUND: PIDs are a heterogeneous group of genetic illnesses, and delay in their diagnosis is thought to be caused by a lack of awareness among physicians concerning PIDs. The latter is what we aimed to evaluate in Brazil. METHODS: Physicians working at general hospitals all over the country were asked to complete a 14-item questionnaire. One of the questions described 25 clinical situations that could be associated with PIDs and a score was created based on percentages of appropriate answers. RESULTS: A total of 4026 physicians participated in the study: 1628 paediatricians (40.4%), 1436 clinicians (35.7%), and 962 surgeons (23.9%). About 67% of the physicians had learned about PIDs in medical school or residency training, 84.6% evaluated patients who frequently took antibiotics, but only 40.3% of them participated in the immunological evaluation of these patients. Seventy-seven percent of the participating physicians were not familiar with the warning signs for PIDs. The mean score of correct answers for the 25 clinical situations was 48.08% (±16.06). Only 18.3% of the paediatricians, 7.4% of the clinicians, and 5.8% of the surgeons answered at least 2/3 of these situations appropriately. CONCLUSIONS: There is a lack of medical awareness concerning PIDs, even among paediatricians, who have been targeted with PID educational programmes in recent years in Brazil. An increase in awareness with regard to these disorders within the medical community is an important step towards improving recognition and treatment of PIDs.


Subject(s)
Clinical Competence/statistics & numerical data , Immunologic Deficiency Syndromes/epidemiology , Physicians/statistics & numerical data , Brazil , Cross-Sectional Studies , General Surgery , Hospitals, General , Humans , Immunologic Deficiency Syndromes/diagnosis , Internal Medicine , Pediatrics , Physician's Role , Professional Practice , Surveys and Questionnaires
3.
Phys Rev E Stat Nonlin Soft Matter Phys ; 70(5 Pt 2): 056309, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15600755

ABSTRACT

A dual lattice vortex formulation of homogeneous turbulence is developed, within the Martin-Siggia-Rose field theoretical approach. It consists of a generalization of the usual dipole version of the Navier-Stokes equations, known to hold in the limit of vanishing external forcing. We investigate, as a straightforward application of our formalism, the dynamics of closed vortex tubes, randomly stirred at large length scales by Gaussian stochastic forces. We find that besides the usual self-induced propagation, the vortex tube evolution may be effectively modeled through the introduction of an additional white-noise correlated velocity field background. The resulting phenomenological picture is closely related to observations previously reported from a wavelet decomposition analysis of turbulent flow configurations.

4.
Phys Rev E Stat Nonlin Soft Matter Phys ; 65(3 Pt 2B): 036302, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11909239

ABSTRACT

We study probability density functions (PDFs) of the circulation of velocity and magnetic fields in magnetohydrodynamics, computed for a circular contour within inertial range scales. The analysis is based on the instanton method as adapted to the Martin-Siggia-Rose field theory formalism. While in the viscous limit the expected Gaussian behavior of fluctuations is indeed verified, the case of vanishing viscosity is not suitable of a direct saddle-point treatment. To study the latter limit, we take into account fluctuations around quasistatic background fields, which allows us to derive a sum rule relating PDFs of the circulation observables and the rate of the strain tensor. A simple inspection of the sum rule definition leads straightforwardly to the algebraic decay rho(Gamma)-1/Gamma(2) at the circulation PDF tails.

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