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1.
Antimicrob Agents Chemother ; 47(8): 2663-5, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12878537

ABSTRACT

Children with acute otitis media underwent tympanocentesis and were given a single dose of 30 mg of azithromycin/kg of body weight. At day 28, the overall clinical cure rate was 206 of 242 (85%). Clinical cure rates for patients infected with Streptococcus pneumoniae (67 of 76; 88%) and Haemophilus influenzae (28 of 44; 64%) were consistent with historical rates for the 5-day dosing regimen.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Azithromycin/therapeutic use , Otitis Media/therapy , Anti-Bacterial Agents/administration & dosage , Azithromycin/administration & dosage , Child, Preschool , Combined Modality Therapy , Drainage , Female , Humans , Infant , Male , Otitis Media/drug therapy , Otitis Media/microbiology
2.
J Pediatr Gastroenterol Nutr ; 34(2): 137-44, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11840030

ABSTRACT

BACKGROUND: Immunologic development of soy-fed infants has not been extensively studied. Early studies of soy flour-based formulas showed decreased immunoglobulin production when soy protein intake was limited. However, there were no significant differences in rotavirus vaccine responses between breast-fed and soy protein isolate-based formula-fed infants. Nucleotides added to milk-based formula benefit infant immune status, but reports of the immunologic effects of adding nucleotides to soy-based formula are not available. This study evaluated immune status and morbidity of infants fed soy protein isolate formulas with and without added nucleotides for 1 year. METHODS: Newborn, term infants enrolled in a masked 12-month feeding trial were assigned randomly to groups fed soy formula with or without added nucleotides (n = 94, n = 92). A nonrandomized human milk/formula cohort (n = 81) was concurrently enrolled. Recommended immunizations were administered at 2, 4, and 6 months. Immune status was determined from antibody responses to Haemophilus influenzae type b, tetanus, diphtheria, and poliovirus vaccines at 6, 7, and 12 months. Parents and physicians reported morbidity data. RESULTS: All vaccine responses were within normal ranges. No response differences were observed between infants fed soy formula and those fed nucleotide-supplemented soy. However, antibody to H. influenzae type b at 7 and 12 months was higher in infants fed nucleotide-supplemented soy than in infants fed human milk/formula ( P = 0.007, P = 0.008, respectively). Human milk/formula-fed infants had higher poliovirus neutralizing antibody at 12 months than did soy-fed infants ( P = 0.016). Morbidity analyses showed that only physician-reported diarrhea was different among groups (groups fed human milk/formula had less diarrhea than did soy groups, P = 0.011). CONCLUSIONS: Term infants fed soy protein isolate-based formulas have normal immune development as measured by antibody responses to childhood immunizations.


Subject(s)
Glycine max , Immune System/drug effects , Infant Food , Nucleotides/administration & dosage , Vaccines/immunology , Antibody Formation , Bottle Feeding , Breast Feeding , Diarrhea, Infantile/etiology , Diarrhea, Infantile/immunology , Double-Blind Method , Female , Food, Fortified , Haemophilus influenzae/immunology , Humans , Infant , Infant, Newborn , Longitudinal Studies , Male , Milk, Human/immunology , Nucleotides/immunology , Poliovirus/immunology
3.
J Pediatr Gastroenterol Nutr ; 34(2): 145-53, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11840031

ABSTRACT

BACKGROUND: Infants fed a soy protein isolate-based formula have immunization responses similar to breast-fed infants. However, cellular aspects of the immunologic development of soy-fed infants have not been studied extensively. Nucleotides added to milk-based formula benefit infant immune status, but reports of the immunologic effects of adding nucleotides to soy-based formula are not available. This study examines immune cell populations of infants fed soy protein isolate formulas with and without added nucleotides for 1 year. METHODS: Newborn, term infants studied in a masked 12-month feeding trial were assigned randomly to soy formula groups with and without added nucleotides (n = 94, n = 92). A nonrandomized human milk/formula-fed cohort (n = 81), was concurrently enrolled. Blood samples were collected at 6, 7, and 12 months. Thirty-two immune cell populations were characterized using three-color flow cytometry. Cellular markers were chosen to assess general pediatric immune status, emphasizing maturation and activation of B, T, and NK lymphocytes. RESULTS: All cell populations, number and percentages, were within age-related normal ranges. The only significant difference found between soy formula and human milk/formula-fed infants was the percentage of CD57 + NK T cells at 12 months (human milk/formula > soy formula, P = 0.034). There were significant differences at some time points between human milk/formula-fed and nucleotide-supplemented soy formula-fed infants in populations of lymphocytes, eosinophils, total T, helper T, naive helper, memory/effector helper, CD57 - T, and CD11b + CD8 + NK cells. None of the cell populations differed between infants fed soy formula versus soy plus nucleotides. CONCLUSIONS: Infants fed this commercial soy formula demonstrated immune cell status similar to human milk/formula-fed infants, consistent with normal immune system development. The addition of nucleotides to soy formula did not significantly change specific individual immune cell populations but tended to increase numbers and percentages of T cells and decreased numbers and percentages of NK cells.


Subject(s)
Immune System/cytology , Immune System/drug effects , Lymphocyte Subsets/immunology , Milk, Human/immunology , Nucleotides/administration & dosage , Nucleotides/immunology , B-Lymphocytes/immunology , Bottle Feeding , Breast Feeding , Cohort Studies , Female , Flow Cytometry , Food, Fortified , Humans , Infant , Infant Food , Infant, Newborn , Killer Cells, Natural/drug effects , Killer Cells, Natural/immunology , Longitudinal Studies , Lymphocyte Count , Male , Glycine max , T-Lymphocytes/drug effects , T-Lymphocytes/immunology
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