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1.
Minerva Pediatr ; 57(4): 173-80, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16172596

ABSTRACT

AIM: Elimination of the offending food is imperative in the management of children with cow-milk allergy/intolerance (CMA/CMI). Herein we report the result of randomized clinical trial carried out to test the efficacy and safety of a new almond-based food (hereinafter named almond milk) in a group of infant with CMI/CMA. METHODS: A group of 52 infants aged 5 to 9 months and with documented CMI/CMA was enrolled and randomized to: almond milk (Group A, n=26); soy-based formula (Group B, n=13); protein hydrolysate-based formula (n=13). The main efficacy outcomes were the improvement in clinical symptoms and the decrease in serum levels of soluble CD30 (a potential marker for atopic disorders; sCD30). RESULTS: Elimination of the offending food and supplementation with a milk protein-free formula produced a considerable improvement of clinical manifestations within 5-12 days in all cases examined (at the onset of the study: 26.4+/-5.4 U/mL and 7.9+/-5.2 U/mL in IgE+ and IgE- infants respectively, after 6 months of supplementation: 16.6+/-4.8 U/mL and 7.1+/-4.5 U/mL in IgE+ and IgE- infants respectively). No difference in growth rate (increment of weight, length and head circumference) was found, during the entire study, between infants given the almond milk and babies given the soy-based formula or the protein hydrolysate-based formula. Supplementation with the soy-based and protein hydrolysate-based formulas caused the development, in some subjects, of a secondary sensitization (23% to soy-based and 15% protein hydrolysate-based formula), whereas supplementation with the almond milk did not. CONCLUSIONS: Though preliminary, the present findings seem to demonstrate that the almond milk may an efficacious substitute of cow milk in infants with CMA/CMI. One could speculate that some active principles contained in the almond milk could contribute to its beneficial effect observed in CMI/CMA-affected infants.


Subject(s)
Milk Substitutes , Milk/adverse effects , Prunus , Animals , Female , Humans , Immunoglobulin E/blood , Infant , Male , Milk Hypersensitivity
3.
Inflamm Res ; 53(11): 601-3, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15693608

ABSTRACT

Familial chronic nail candidiasis (FCNC.MIM 607644) is a rare disorder characterized by early onset infections caused by different species of Candida and restricted to the nails; this disorder is genetically associated with low serum concentration of intercellular adhesion molecule 1 (ICAM-1). Herein we report the evidence of high circulating levels of malondialdehyde (MDA) and 4-hydroxy-2,3-nonenal (HNE) in seven patients of a five-generation Italian family affected by FCNC.MIM 607644. The present data evidence, in these patients, an increase in circulating MDA and HNE levels. Only some merely speculative hypotheses may be suggested to explain the mechanisms subserving the oxidative stress condition observed in these genetically ICAM-1 deficient patients; however, one has to point out that a chronic oxidative stress condition could contribute to the development of concurrent pathological alterations in which an overproduction of free radicals may play a central role.


Subject(s)
Aldehydes/blood , Candidiasis, Chronic Mucocutaneous/diagnosis , Malondialdehyde/blood , Nail Diseases/diagnosis , Oxidative Stress , Adolescent , Adult , Biomarkers/blood , Candidiasis, Chronic Mucocutaneous/blood , Candidiasis, Chronic Mucocutaneous/metabolism , Child , Female , Humans , Intercellular Adhesion Molecule-1/metabolism , Italy , Male , Middle Aged , Nail Diseases/blood , Nail Diseases/metabolism
5.
Mediators Inflamm ; 12(4): 247-9, 2003 Aug.
Article in English | MEDLINE | ID: mdl-14514476

ABSTRACT

Familiar chronic nail candidiasis (FCNC) is a rare disorder characterized by early-onset infections caused by different species of Candida, restricted to the nail of the hands and feet, and associated with a low serum concentration of intercellular adhesion molecule 1. Host defense mechanisms against candidiasis require the cooperation of many immune cells through several candidacidal mechanisms, including oxygen-dependent killing mechanisms, mediated by a superoxide anion radical myeloperoxidase--H2O2--halide system, and reactive nitrogen intermediates. We analyzed protein carbonyl groups (considered a useful marker of oxidative stress) in the serum of patients belonging to a five-generation Italian family with an isolated form of FCNC. Serum protein carbonyl groups in FCNC patients were significantly lower than those measured in healthy donors. Also, if this hypothesis is merely speculative, we could suggest that the decreased circulating level of protein carbonyl groups in these patients is not a marker of a lower oxidative stress condition, but might be linked to a lower protease activity.


Subject(s)
Blood Proteins/chemistry , Candidiasis, Chronic Mucocutaneous/blood , Nails/microbiology , Oxidative Stress , Adolescent , Adult , Biomarkers , Child , Child, Preschool , Female , Humans , Intercellular Adhesion Molecule-1/blood , Italy , Male , Middle Aged , Superoxides/metabolism
6.
Eur J Hum Genet ; 11(6): 433-6, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12774035

ABSTRACT

Chronic mucocutaneous candidiases (CMC) are a group of rare disorders where an altered immune response against Candida leads to persistent and/or recurrent infections of the skin, nails, and mucous membranes. We analysed a five-generation Italian family with an isolated form of CMC, affecting nails only, in the presence of low serum concentration of intercellular adhesion molecule I (ICAM-1). We excluded linkage to candidate regions on chromosomes 2p (CMC with thyroid disease), 21q22.3 (APECED), and 19q13 (ICAM-1). We then carried out a genome-wide scan and assigned the CMC locus to a 19 cM pericentromeric region on chromosome 11.


Subject(s)
Candidiasis, Chronic Mucocutaneous/genetics , Chromosome Mapping , Chromosomes, Human, Pair 11/genetics , Humans , Intercellular Adhesion Molecule-1/genetics , Italy , Pedigree
8.
J Pediatr Surg ; 37(5): 741-4, 2002 May.
Article in English | MEDLINE | ID: mdl-11987091

ABSTRACT

BACKGROUND/PURPOSE: Surgical stress produces changes in the immune status of patients. In adults, major surgery causes immunosuppression, whereas minor operations stimulate immune responses. In children, the immunologic response to surgery has not been elucidated completely. The authors investigated the effects of minor surgery on immune response by analyzing neutrophil and monocyte phagocytosis and oxidative burst activity. METHODS: Sixteen children undergoing elective minor surgery were enrolled. Blood samples were collected before the operation (at time of induction of anesthesia), at the end of operation, and 72 hours after surgery. Neutrophil and monocyte phagocytosis and oxidative burst activity were studied using a flow cytometric method. RESULTS: Phagocytosis and oxidative burst increased significantly at the end of the operation, both in neutrophils (7.4% and 14.3%, respectively) and monocytes (11.6% and 27%, respectively). The increase was only significant for monocytes (17.5%) 72 hours after surgery. White cell count did not show any significant changes. There was no significant correlation between phagocytosis, oxidative burst activity, and white cell count or neutrophil and monocyte count. CONCLUSIONS: This study shows that minor surgery in children induces immune activation by increasing neutrophil and monocyte phagocytosis and oxidative burst activity. Further studies are required to understand the molecular basis of these findings.


Subject(s)
Monocytes/immunology , Neutrophils/immunology , Surgical Procedures, Operative , Adolescent , Child , Humans , Laparotomy , Length of Stay , Neutrophil Activation/physiology , Phagocytosis/immunology , Prospective Studies , Respiratory Burst/immunology , Stress, Physiological/immunology , Wounds, Penetrating/immunology
9.
Minerva Pediatr ; 53(1): 1-5, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11309536

ABSTRACT

BACKGROUND: Serum IgD and IgE levels were measured in children with atopic asthma and in control Group in order to determine their relationship with clinical status. METHODS: Samples of venous blood (of 5 cc) were drawn from 25 asthmatic children (Group A) and 25 healthy children (Group B) at the moment of first diagnosis (T0), after 6 months (T180) and after 18 months (T540). To measure IgD, an ELISA assay based on the sandwich principle was used. RESULTS: At T0, IgD were significantly higher in Group A (182.7 5+/-88.18 IU/ml) in comparison with Group B (69.58+/-4.93 IU/ml, p<0.0001); IgD levels decreased in Group A at T540. CONCLUSIONS: In conclusion, a significant increase of IgD levels observed in children at first signs of asthma and the following normalization of these same levels after 18 months, may represent a non specific response or an attempt of the organism to block asthma, favouring therefore immunologic tolerance.


Subject(s)
Asthma/blood , Immunoglobulin D/blood , Age Factors , Allergens , Asthma/immunology , Child , Child, Preschool , Data Interpretation, Statistical , Enzyme-Linked Immunosorbent Assay , Female , Follow-Up Studies , Humans , Immunoglobulin E/blood , Longitudinal Studies , Male , Time Factors
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