Modulation of the immune system by human milk and infant formula containing nucleotides

被引:184
作者
Pickering, LK
Granoff, DM
Erickson, JR
Masor, ML
Cordle, CT
Schaller, JP
Winship, TR
Paule, CL
Hilty, MD
机构
[1] Eastern Virginia Med Sch, Childrens Hosp Kings Daughters, Ctr Pediat Res, Norfolk, VA 23510 USA
[2] Childrens Hosp Oakland, Res Inst, Oakland, CA 94609 USA
[3] Univ Arizona, Tucson, AZ USA
[4] Abbott Labs, Ross Prod Div, Columbus, OH USA
关键词
antibody; breast milk; diphtheria; H influenzae b; human milk; immune development; immune response; infant formula; nucleotides; polio; vaccine response;
D O I
10.1542/peds.101.2.242
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective. To determine whether human milk and nucleotides added to infant formula at levels present in human milk enhance development of the immune system during infancy. Methods. A 12-month, controlled, randomized and blinded, multisite feeding trial was conducted on two infant formulas: iron-fortified, milk-based control formula (Control) or the same formula fortified with nucleotides (Nucleotide). The level (72 mg/L) and ratio of individual nucleotides selected were patterned after those available in human milk. A third group fed human milk exclusively for 2 months and then human milk or Similac with iron until 12 months of age also was studied. Response to immunizations was chosen to assess development of the immune system. Infants followed the immunization schedule recommended by the American Academy of pediatrics in 1991. Outcome Variables. Antibody responses were determined at 6, 7, and 12 months of age to Haemophilus influenzae type b polysaccharide (Hib), to diphtheria and tetanus toxoids, and to oral polio virus (OPV) immunizations. Results. Of 370 full-term, healthy infants enrolled, 311 completed the study (107 Control, 101 Nucleotide, 103 human milk/Similac with iron). Intake, tolerance, and growth of infants were similar in all three groups. Compared with the Control group 1 month after the third immunization (7 months of age), the Nucleotide group had a significantly higher Hib antibody concentration (geometric mean concentrations of 7.24 vs 4.05 mu g/mL, respectively), and a significantly higher diphtheria antibody concentration (geometric mean of 1.77 vs 1.38 U/mL). The significantly higher Hib antibody response in the Nucleotide group persisted at 12 months. The antibody responses to tetanus and OPV were not enhanced by nucleotide fortification. There also was an effect of breastfeeding on immune response. Infants who breastfed had significantly higher neutralizing antibody titers to polio virus than either formula-fed group (1:346 vs 1:169 and 1:192 in the Control and Nucleotide groups, respectively) at 6 months of age. Conclusion. Infant formula fortified with nucleotides enhanced H influenzae type b and diphtheria humoral antibody responses. Feeding human milk enhanced antibody response to OPV. Dietary factors play a role in the antibody response of infants to immunization.
引用
收藏
页码:242 / 249
页数:8
相关论文
共 58 条
  • [1] ALBRECHT P, 1984, REV INFECT DIS, V6, pS540
  • [2] BACTERICIDAL AND OPSONIC ACTIVITY OF IGG1 AND IGG2 ANTICAPSULAR ANTIBODIES TO HAEMOPHILUS-INFLUENZAE TYPE-B
    AMIR, J
    SCOTT, MG
    NAHM, MH
    GRANOFF, DM
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (01) : 163 - 171
  • [3] EFFECT OF DIETARY NUCLEOTIDE SUPPLEMENTATION ON DIARRHEAL DISEASE IN INFANTS
    BRUNSER, O
    ESPINOZA, J
    ARAYA, M
    CRUCHET, S
    GIL, A
    [J]. ACTA PAEDIATRICA, 1994, 83 (02) : 188 - 191
  • [4] EFFECT OF DIETARY NUCLEOTIDES ON SMALL-INTESTINAL REPAIR AFTER DIARRHEA - HISTOLOGICAL AND ULTRASTRUCTURAL-CHANGES
    BUENO, J
    TORRES, M
    ALMENDROS, A
    CARMONA, R
    NUNEZ, MC
    RIOS, A
    GIL, A
    [J]. GUT, 1994, 35 (07) : 926 - 933
  • [5] CARVER J, 1993, FASEB J, V4, pA643
  • [6] CARVER JD, 1991, PEDIATRICS, V88, P359
  • [7] CARVER JD, 1995, NUTR BIOCH, V6, P58
  • [8] EFFECT OF BREAST-FEEDING ON RESPONSES OF SYSTEMIC INTERFERON AND VIRUS-SPECIFIC LYMPHOCYTE-TRANSFORMATION IN INFANTS WITH RESPIRATORY SYNCYTIAL VIRUS-INFECTION
    CHIBA, Y
    MINAGAWA, T
    MITO, K
    NAKANE, A
    SUGA, K
    HONJO, T
    NAKAO, T
    [J]. JOURNAL OF MEDICAL VIROLOGY, 1987, 21 (01) : 7 - 14
  • [9] CIRNE MD, 1995, J INFECT DIS, V171, P1097, DOI 10.1093/infdis/171.5.1097
  • [10] *COMM INF DIS, 1991, REP COMM INF DIS