Fitzsimmons S P, Evans M K, Pearce C L, Sheridan M J, Wientzen R, Cole M F
Department of Microbiology, Georgetown University Medical Center, Washington, D.C.
J Pediatr. 1994 Apr;124(4):566-73. doi: 10.1016/s0022-3476(05)83135-x.
We sought to determine (1) the ontogeny of secretory IgA subclasses in saliva of breast- and formula-fed infants and (2) the influence of breast-feeding on the maturation of secretory salivary IgA subclasses. Secretory IgA and subclasses 1 and 2 concentrations were determined in saliva from 40 healthy, term infants from birth to age 18 months, and in parallel milk samples from the infants' mothers who were breast-feeding during the first 6 months after birth. Secretory IgA was detected in the neonates' saliva as early as 3 days after birth, increased rapidly during the next 6 months, but then stabilized at a level approximately one-sixth that of the mothers' salivary secretory IgA. Secretory IgA2 represented less than 15% of secretory IgA in saliva collected 2 weeks after birth but by 6 months represented 24.4% of secretory IgA, a value approaching that of the mothers' salivary secretory IgA2 (30.4%). This increase in the proportion of secretory IgA2 was temporally related to a reduction in the proportion of secretory IgA2 in milk throughout lactation. The secretory IgA concentration increased more rapidly during the first 6 months after birth in infants exclusively breast fed than in those exclusively bottle fed. We conclude that although secretory immunity is immature in infants, breast-feeding may aid in protection against pathogenic microorganisms by increasing the rate of mucosal IgA maturation.
(1)母乳喂养和配方奶喂养婴儿唾液中分泌型IgA亚类的个体发生情况;(2)母乳喂养对唾液分泌型IgA亚类成熟的影响。测定了40名足月健康婴儿从出生到18个月龄时唾液中的分泌型IgA及其1类和2类亚类的浓度,并同时测定了在出生后头6个月进行母乳喂养的母亲的乳汁样本。早在出生后3天就在新生儿唾液中检测到了分泌型IgA,在接下来的6个月中迅速增加,但随后稳定在母亲唾液分泌型IgA水平的约六分之一。出生后2周收集的唾液中,分泌型IgA2占分泌型IgA的比例不到15%,但到6个月时占分泌型IgA的24.4%,这一数值接近母亲唾液分泌型IgA2的比例(30.4%)。分泌型IgA2比例的增加在时间上与整个哺乳期乳汁中分泌型IgA2比例的降低相关。与完全人工喂养的婴儿相比,完全母乳喂养的婴儿在出生后的头6个月中分泌型IgA浓度增加得更快。我们得出结论,尽管婴儿的分泌性免疫不成熟,但母乳喂养可能通过提高黏膜IgA成熟率来帮助抵御致病微生物。