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1.
Proc Biol Sci ; 291(2017): 20232541, 2024 Feb 28.
Article in English | MEDLINE | ID: mdl-38378149

ABSTRACT

Inter-individual transmission of cancer cells represents a unique form of microparasites increasingly reported in marine bivalves. In this study, we sought to understand the ecology of the propagation of Mytilus trossulus Bivalve Transmissible Neoplasia 2 (MtrBTN2), a transmissible cancer affecting four Mytilus mussel species worldwide. We investigated the prevalence of MtrBTN2 in the mosaic hybrid zone of M. edulis and M. galloprovincialis along the French Atlantic coast, sampling contrasting natural and anthropogenic habitats. We observed a similar prevalence in both species, probably due to the spatial proximity of the two species in this region. Our results showed that ports had higher prevalence of MtrBTN2, with a possible hotspot observed at a shuttle landing dock. No cancer was found in natural beds except for two sites close to the hotspot, suggesting spillover. Ports may provide favourable conditions for the transmission of MtrBTN2, such as high mussel density, stressful conditions, sheltered and confined shores or buffered temperatures. Ships may also spread the disease through biofouling. Our results suggest ports may serve as epidemiological hubs, with maritime routes providing artificial gateways for MtrBTN2 propagation. This highlights the importance of preventing biofouling on docks and ship hulls to limit the spread of marine pathogens hosted by fouling species.


Subject(s)
Mytilus , Neoplasms , Animals , Neoplasms/epidemiology
2.
Article in English | MEDLINE | ID: mdl-32577121

ABSTRACT

BACKGROUND: The role and importance of skin barrier as an immunologic organ and as a potent way of sensitization is well known. However, antibiotics anaphylaxis following skin sensitization has not been reported. CASE PRESENTATION: We describe the first case of intravenous clindamycin anaphylaxis, with likely sensitization due to previous topical exposure to clindamycin gel for acne in a 14-year-old boy with history of atopy and mild atopic dermatitis. CONCLUSION: This case highlights the potential sensitization to drug allergens, including antibiotics, via the skin.

3.
Eur J Clin Nutr ; 71(2): 287-289, 2017 02.
Article in English | MEDLINE | ID: mdl-28000691

ABSTRACT

Egg is an ubiquitous allergen found in many food products. Current food allergy guidelines recognize the importance of consultation with a registered dietitian to ensure nutritional adequacy. However, there is a lack of evidence on its impact on the implementation of allergen avoidance strategies. Taking advantage of a well-characterized cohort of influenza vaccination in egg-allergic children (n=397), we tested the hypothesis that real-life professional dietary advice was associated with a decrease in accidental reactions to egg in allergic children with retrospective questionnaires. Lack of consultation with a dietitian was associated with a 1.89-fold increase in the risk of accidental reactions to egg (confidence interval: 1.47-2.42). The only other independent variable that predicted reactions was having had a history of acute reaction to egg prior diagnosis (relative risk=2.02; confidence interval: 1.64-3.00). These findings support the usefulness of referral to a food allergy-specialized dietitian at time of diagnosis in order to prevent future accidental reactions to egg.


Subject(s)
Accident Prevention/methods , Anaphylaxis/prevention & control , Egg Hypersensitivity/therapy , Nutritionists/statistics & numerical data , Referral and Consultation/statistics & numerical data , Anaphylaxis/etiology , Child , Egg Hypersensitivity/complications , Female , Humans , Influenza Vaccines , Male , Retrospective Studies , Surveys and Questionnaires
4.
Allergy ; 71(12): 1762-1771, 2016 12.
Article in English | MEDLINE | ID: mdl-27291651

ABSTRACT

BACKGROUND: The prevalence of peanut allergy in younger siblings of children with peanut allergy has been reported between 7% and 8.5%, but the anaphylactic risk at the time of introduction is currently unknown, which limits our ability to best counsel parents on this issue. OBJECTIVE: To determine the risk of anaphylaxis and working parameters of allergy testing in this context. METHODS: One hundred and fifty-four peanut-naïve younger siblings of peanut-allergic children underwent double-blinded skin testing, followed by parent-led peanut introduction. Questionnaires were dispensed to parents to investigate preferences with regard to peanut introduction in this subgroup. RESULTS: Eight participants (5.2%) presented unequivocal IgE-mediated reactions to peanut upon introduction, including five anaphylaxes. These participants were significantly older compared to the rest of the cohort (median 4.0 vs 1.9 years, P = 0.04). The negative predictive value of skin prick test with peanut extract and peanut butter and of specific IgE was 99%, 100%, and 100%, respectively. Six peanut-tolerant participants had positive peanut allergy tests. The option of introducing at home without prior skin testing was associated with high levels of anxiety (median 8.4 on 10-point Likert scale) when compared to supervised introduction (median 3.8, P < 0.0001) or home introduction after negative skin test (median 4.3, P < 0.0001). CONCLUSIONS: There is an increased risk of anaphylaxis upon peanut introduction in siblings of children with peanut allergy, and parents are reluctant to introduce at home without testing. Allergy testing prior to introduction is negative in over 90% of cases and carries a high negative predictive value.


Subject(s)
Allergens/immunology , Arachis/adverse effects , Peanut Hypersensitivity/epidemiology , Peanut Hypersensitivity/immunology , Siblings , Age Factors , Allergens/administration & dosage , Anaphylaxis/epidemiology , Anaphylaxis/immunology , Child, Preschool , Comorbidity , Diagnostic Tests, Routine , Diet , Female , Humans , Immunoglobulin E/immunology , Infant , Male , Peanut Hypersensitivity/diagnosis , Peanut Hypersensitivity/therapy , Predictive Value of Tests , Prospective Studies , Risk , Skin Tests
8.
J Investig Allergol Clin Immunol ; 20(4): 289-94, 2010.
Article in English | MEDLINE | ID: mdl-20815306

ABSTRACT

BACKGROUND: Peanut allergy is an important public health problem in western countries. However, the risk factors associated with this allergy remain uncertain. OBJECTIVE: To determine whether the consumption of peanuts during pregnancy and breastfeeding is a risk factor for peanut allergy in infants. METHODS: We enrolled 403 infants in a case-control study. The cases were infants aged 18 months or less with a diagnosis of peanut allergy based on a history of clinical reaction after exposure to peanuts and the presence of peanut-specific immunoglobulin E. Controls were age-matched infants with no known clinical history or signs of atopic disease. The mothers of the children filled out a detailed questionnaire about maternal diet during pregnancy and breastfeeding, the infant's diet, the presence of peanut products in the infant's environment, and family history of atopy. RESULTS: The mean (SD) age of cases was 1.23 (0.03) years. The groups were comparable in terms of the rate and duration of breastfeeding. However, the reported consumption of peanuts during pregnancy and breastfeeding was higher in the case group and associated with an increased risk of peanut allergy in offspring (odds ratio [OR], 4.22 [95% confidence interval [CI], 1.57-11.30 and OR, 2.28 [95% CI, 1.31-3.97] for pregnancy and breastfeeding, respectively). Overall, the infants with peanut allergy did not seem to be more exposed to peanut products in their environment than the controls. CONCLUSION: Early exposure to peanut allergens, whether in utero or through human breast milk, seems to increase the risk of developing peanut allergy.


Subject(s)
Antigens, Plant/metabolism , Breast Feeding/epidemiology , Fetomaternal Transfusion/immunology , Peanut Hypersensitivity/epidemiology , Prenatal Exposure Delayed Effects/epidemiology , Adult , Antigens, Plant/immunology , Breast Feeding/adverse effects , Case-Control Studies , Female , Humans , Immunization , Infant , Infant, Newborn , Male , Maternal Exposure/adverse effects , Peanut Hypersensitivity/diagnosis , Peanut Hypersensitivity/immunology , Peanut Hypersensitivity/physiopathology , Pregnancy , Prenatal Exposure Delayed Effects/diagnosis , Prenatal Exposure Delayed Effects/immunology , Prenatal Exposure Delayed Effects/physiopathology , Prenatal Nutritional Physiological Phenomena/immunology , Risk Factors
13.
J Allergy Clin Immunol ; 107(1): 73-80, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11149994

ABSTRACT

BACKGROUND: Chronic rhinosinusitis is a common comorbidity of asthma. However, sinonasal involvement in severe steroid-dependent asthma is still undefined. OBJECTIVE: The aim of the study was to evaluate chronic rhinosinusitis in 35 patients with severe steroid-dependent asthma by using a clinical score and coronal computed tomography (CT) scanning. METHODS: Thirty-five subjects (16 female subjects) with severe asthma requiring daily doses of oral corticosteroids were compared with 34 patients (19 female patients) with mild-to-moderate asthma. Sinonasal involvement was studied by using clinical and CT scores. Airflow obstruction, therapy requirement, and asthma triggering factors were carefully assessed. RESULTS: The proportion of patients with symptoms of rhinosinusitis was similar in both groups of asthmatic subjects (74% in patients with severe steroid-dependent asthma and 70% in patients with mild-to-moderate asthma). All subjects with steroid-dependent asthma versus 88% of subjects with mild-to-moderate asthma had abnormal CT scan results. The clinical (P <.05) and CT scan (P <.0005) severity scores were higher in the subjects with severe steroid-dependent asthma. In both groups the CT scan scores were correlated to the clinical scores (P <.0001 and P <.006), but only in the mild-to-moderate group were both scores correlated with high significance (P <.002 and P <.0005) to the absolute number of blood eosinophils. CONCLUSION: Frequency of rhinosinusitis in patients with mild-to-moderate or severe steroid-dependent asthma is similar; however, sinonasal involvement, as evaluated by clinical symptoms and CT scan imaging, is significantly greater in the patients with severe steroid-dependent asthma than in those with mild-to-moderate asthma.


Subject(s)
Asthma/complications , Rhinitis/complications , Sinusitis/complications , Adolescent , Adult , Child , Humans , Nasal Cavity/diagnostic imaging , Paranasal Sinuses/diagnostic imaging , Severity of Illness Index , Tomography, X-Ray Computed
14.
Ultrasonics ; 38(1-8): 537-41, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10829722

ABSTRACT

In the aim of simulating the ultrasonic inspection of multilayered structure, we propose a hybrid model, based on transfer matrices and ray tracing formalisms. This approach allows one to predict the response of structures containing defects of finite size such as delaminations or adhesion defect.

16.
J Allergy Clin Immunol ; 102(4 Pt 1): 571-8, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9802364

ABSTRACT

BACKGROUND: Cells producing a T(H2)-cytokine profile play an important role in the onset and maintenance of atopic diseases, and therefore specific immunotherapy is aimed to induce a switch to cells producing a T(H1)- or T(H0)-cytokine profile. Recently, a novel form of immunotherapy making use of synthetic peptides from the major cat allergen Fel d 1 has been developed, but its mechanisms of action are unknown. OBJECTIVES: We examined the effects of immunotherapy with Fel d 1 peptides on the response to bronchial provocation tests (PD20FEV1) with a standardized Fel d 1 cat extract on Fel d 1-specific serum IgE and IgG levels and in vitro IL-4 and IFN-gamma production. METHODS: Patients allergic to cats received 6 weekly injections of 7.5 micro(g) (low dose), 75 micro(g) (medium dose), or 750 micro(g) (high dose) of Fel d 1 peptides (25 patients) or a placebo (6 patients). RESULTS: Six weeks after ending immunotherapy, posttreatment PD20FEV1 was not significantly different between the treated and placebo groups. However, in the medium- and high-dose groups there was a significant improvement between baseline and posttreatment days. IL-4 release was significantly reduced in the high dose-treated group (P <.005, Wilcoxon W test), whereas it was unchanged in the low or medium dose- and in the placebo-treated groups. In all groups, IFN-gamma, IgE, and IgG levels remained unchanged. CONCLUSION: There was no correlation between the improvement of PD20FEV1 and the decrease in IL-4 production. These data suggest that peptide immunotherapy may act by shifting the Fel d 1-induced response of PBMCs in vitro from the T(H2)-like to the T(H0)-like phenotype.


Subject(s)
Allergens/therapeutic use , Desensitization, Immunologic , Glycoproteins/therapeutic use , Interleukin-4/blood , T-Lymphocytes/metabolism , Adult , Animals , Basophils/metabolism , Bronchial Provocation Tests , Cats , Dose-Response Relationship, Drug , Double-Blind Method , Female , Glycoproteins/administration & dosage , Humans , Immunoglobulin E/biosynthesis , Immunoglobulin G/biosynthesis , Interferon-gamma/blood
18.
J Allergy Clin Immunol ; 99(4): 450-3, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9111487

ABSTRACT

BACKGROUND: The natural history of allergic sensitization is complex and poorly understood. A prospective nonrandomized study was carried out in a population of asthmatic children younger than 6 years of age whose only allergic sensitivity was to house dust mites (HDMs). OBJECTIVES: The study was designed to determine whether specific immunotherapy (SIT) with standardized allergen extracts could prevent the development of new sensitizations over a 3-year follow-up survey. METHODS: We studied 22 children monosensitized to HDM who were receiving SIT with standardized allergen extracts and 22 other age-matched control subjects who were monosensitized to HDM. The initial investigation included a full clinical history, skin tests with a panel of standardized allergens, and the measurement of allergen-specific IgE, depending on the results of skin tests. Children were followed up on an annual basis for 3 years, and the development of new sensitizations in each group was recorded. RESULTS: Ten of 22 children monosensitized to HDM who were receiving SIT did not have new sensitivities compared with zero of 22 children in the control group (p = 0.001, chi square test). CONCLUSIONS: This study suggests that SIT in children monosensitized to HDM alters the natural course of allergy in preventing the development of new sensitizations.


Subject(s)
Antigens/administration & dosage , Desensitization, Immunologic/methods , Glycoproteins/administration & dosage , Immunization , Mites/immunology , Animals , Antigens, Dermatophagoides , Asthma/diagnosis , Asthma/immunology , Asthma/therapy , Case-Control Studies , Child , Child, Preschool , Desensitization, Immunologic/statistics & numerical data , Female , Humans , Male , Prospective Studies , Skin Tests , Statistics, Nonparametric
19.
Eur Respir J ; 10(4): 958-60, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9150342

ABSTRACT

Eighteen years after an uneventful renal transplantation, the chest radiograph of an asymptomatic 50 year old man showed diffuse bilateral infiltrations, predominately at the right apex. Computed tomography (CT) scan demonstrated a diffuse alveolar pattern, the alveoli being filled with a very dense material, with some tracheal calcifications. Bronchoalveolar lavage fluid analysis was normal, but bronchial and transbronchial biopsies revealed calcium deposits in the bronchial mucosa and in the alveolar septa. The diagnosis of diffuse pulmonary calcinosis was established, despite normal blood calcium, phosphorus and magnesium levels, based upon computed tomography scan and pathological findings at fibreoptic bronchoscopy, without the need for an open lung biopsy.


Subject(s)
Biopsy/methods , Calcinosis/diagnosis , Kidney Transplantation , Lung Diseases/diagnosis , Bronchoscopy , Calcinosis/etiology , Humans , Lung Diseases/etiology , Male , Middle Aged , Tomography, X-Ray Computed
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