Immunologic Factors in Human Milk and Disease Prevention in the Preterm Infant
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- Gregory, K.E. & Walker, W.A. Curr Pediatr Rep (2013) 1: 222. doi:10.1007/s40124-013-0028-2
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Exposure to the immunologic factors found in maternal breast milk has been shown to compensate for the immature immune system that characterizes the preterm infant. Feeding preterm infants with human milk not only provides protection from disease pathogenesis and ensures an optimal source of nutrients in the short term, but it also helps to ensure the development of a healthy immune response in the long term. Here, we review the immunological significance and antiinflammatory effects of a selection of the bioactive molecules found in human milk and how they may differ under conditions of preterm birth. In addition, the role that human milk plays in the intestinal colonization of the preterm infant and why this is important to short- and long-term health outcomes are discussed.
KeywordsBreast milkPreterm infantImmunologyIntestinal colonizationCytokinesAntibodies
Human milk has been recommended as the optimal and exclusive source of early nutrition for all infants following birth and until at least 6 months of age [1, 2]. Human milk is the ideal source of early infant nutrition as a result of potent immune factors and a unique composition of nutrients that evolve in tandem with the growth and developmental needs of the infant. For infants who are born preterm, exposure to the immune factors of human milk is of paramount importance as these infants are born with an immature immune system. For these infants, human milk not only provides protection from disease pathogenesis in the short term, but it also helps to ensure the development of a healthy immune response in the long term. In this article, we will provide an overview of what is known about the immunological profile of preterm infants and review in depth the immunological factors found in human milk that are important for disease prevention and health.
Immunological Profile of the Preterm Infant
Preterm birth (PTB), defined as birth occurring prior to 37 weeks of gestation , persists as a leading perinatal health problem facing women and children. The causes are not fully understood, and preventative measures are lacking [4–6]. The PTB rate is currently reported at 12.8 % of all births in the USA [7, 8] and affects as many as 15 million infants worldwide . The implications of PTB on human health have been well documented [10–17]. One of the leading causes of morbidity and mortality among infants born preterm is infection (bacteremia, pneumonia, meningitis) during the early neonatal period, occurring approximately in one in six infants. A disproportionate number of fatal infections occur in the smallest and most premature infants [18, 19] who require invasive interventions disrupting the protective mucosal and epithelial barriers in the face of inadequate innate immunity .
Innate Immunity in the Preterm Infant
Innate immunity is of primary importance during early life while a fully functional adaptive immune system is developing through interactions with the environment at the mucosal surfaces. The innate immune system specific to the preterm infant is characterized by developmental immaturities that include deficiencies in the number and function of white blood cells, reduced pattern-recognition receptors (PRR) such as Toll-like receptors (TLRs), and limited tight junction (TJ) function of defensins such as Paneth cells [20, 21]. These characteristics common to the preterm infant result in an inadequate extracellular elimination of bacterial infections and aberrant recruitment of immune cells to the site of infection or inflammation . Factors such as TLR4, MD-2, a molecule that participates in the LPS response on TLR4, and other components of the innate immune system are found in human milk and, in the case of the preterm infant, may provide an innate immune response that would not otherwise exist.
Infants who are born preterm start life at an immunological disadvantage when compared to their full-term counterparts, who receive maternal antibodies that are transferred via the placenta during the later stages of pregnancy [23, 24]. Preterm infants are also prone to aberrant intestinal colonization as a result of routine use of antibiotics at birth, often limited exposure to breast milk, increased incidence of birth by Cesarean section, and prolonged hospitalization during early infancy. These factors place infants at a microbial disadvantage and high-risk for inflammatory immune diseases [25, 26], both in the early neonatal period and later in life. Exposure to the immunological factors found in maternal breast milk has been shown to contribute to the development of a more optimal immune response in the preterm infant, thereby overcoming some of the deficiencies of the innate immune function.
Immunological Factors Found in Human Milk
Immunoglobulin-producing B cells are not fully functional at birth, which causes a delayed activation of B cells and, in turn, delayed maturation of antibody-producing plasma cells. These delays result in a temporary deficit of secretory IgA (SIgA) production. This deficit is especially problematic for the preterm infant because SIgA is not absorbed by the neonatal gut, allowing these antibodies to protect the infant’s intestinal mucosa from potentially harmful pathogens. Thus, the absence of SIgA leaves the preterm intestinal mucosa highly vulnerable to pathogenic microorganisms.
SIgA has been measured and compared in the colostrum and mature milk of women who deliver preterm and or at term. These studies have shown that there is significantly more SIgA in the breast milk of women who deliver preterm, with the highest concentrations in the colostrum of women who deliver early [28•, 29, 30]. SIgA concentrations have been shown to taper over time. This taper is slower and more gradual in the milk of women who deliver preterm when compared to that of women who deliver at term . It is speculated that an immunological adaptive response may be present in the breast milk of women who deliver preterm, providing protection to the preterm intestinal mucosa from microorganisms.
IgG is of importance to the preterm infant for its opsonization and agglutination mechanism in pathogen protection. IgG is transferred from the mother to the fetus via the placenta during the later stages of pregnancy, thereby providing immune protection to the fetus and the neonate. Infants who are born preterm do not receive the full benefit of this immune protection and are IgG deficient at birth when compared to their full-term counterparts. IgG, much like SIgA, while found in small concentrations in breast milk, is of great importance to the preterm infant. Past studies have shown that IgG is detected in the majority of colostrum samples and that the concentrations of this antibody are similar in the colostrum of women who deliver preterm and at term [32–34]. However, more recent studies suggest that IgG is higher in the colostrum obtained from women who give birth prior to 32 weeks gestation . Evidence suggests that an IgG Fc receptor is expressed on the luminal surface of the enterocytes in the fetal human intestine . These receptors may function after birth as a transport system for IgG, facilitating the uptake of IgG in breast milk, contributing to the immune response of the premature infant. These findings reinforce the speculation that there may be a unique adaptive response mechanism associated with the lactation pattern of women who deliver preterm.
The neonatal immune system is capable of producing IgM in response to pathogens. Thus, it is not surprising that the IgM concentration in colostrum is low, and detected in approximately 20 % of samples . In studies that have evaluated IgM in the milk of women who deliver at different points in gestation, no significant differences have been observed in the concentrations of IgM in the milk [31, 33, 34, 36].
Breast milk functions to influence the immunological development of the infant through the action of cytokines, one of the most important bioactive components found in human milk. Cytokines are pluripotent polypeptides that act as chemical messengers among cells. These proteins operate in a complex stepwise approach, producing a cascade of effects that contribute to the development and function of the immune system. Cytokines regulate the inflammatory responses stimulated by an antigenic challenge. Through the use of immunoassays, several cytokines have been measured in human milk [28•, 37, 38, 39•]. The majority of research conducted on cytokines in human milk has been done using milk obtained from women who gave birth to full-term infants. However, measurements of milk from women who gave birth to preterm infants show important differences in the cytokine profile that vary with length of gestation.
IL-6 is a cytokine with both pro- and antiinflammatory functions important to the immune system. IL-6 has been highly correlated with IgA, TGF-β1, and TGF-β2 in the milk from women following PTB. These findings support the hypothesis that IL-6 plays a significant role in the development and differentiation of IgA-producing cells [37, 40]. When measured in colostrum, transitional milk, and mature milk obtained from women who deliver at term or prematurely, IL-6 has been shown to be highest in the colostrum, tapering off as the milk matures [28•, 41]. Interestingly, when cytokines were measured in the milk obtained from women after birth at different points of gestation, the highest concentrations of IL-6 were observed between 30 weeks and term, and then lowest concentrations prior to 30 weeks of gestation. Slightly different results have been reported from a study that compared IL-6 in the milk of women who deliver very preterm (24–31 weeks) with that of women who deliver at term (38–41 weeks). IL-6 was found to be higher in the transitional breast milk of women in the very preterm group when compared to the term group; however, this difference decreased in mature milk, suggesting that cytokine content of breast milk decreases with ongoing lactation [39•]. In addition, although IL-6 was higher in the preterm group, multiple regression analysis conducted in this study indicated that the difference was not associated with gestational age at birth, but cesarean delivery. Other discrepancies among studies may be explained by how colostrum, transitional, and mature milk are defined, as well as how infants are classified based on their gestational age at birth.
Overall, the findings relative to IL-6 suggest that human milk may have the ability to compensate for the immunological immaturity common to premature infants, but perhaps only after a certain point in gestation. Thus, infants born extremely preterm (i.e., before 30 weeks) appear to be at an even greater immunological disadvantage; not only is their immature immune system ill prepared for the extrauterine environment, but also the compensatory properties found in human milk that support development of the immune system and protection from infection are less abundant.
IL-8 is typically secreted by macrophages, cells with TLRs that are involved in the innate immune response. For preterm infants, who have a delayed innate immune system that is slow to respond to antigens, exposure to IL-8 in human milk is of great importance. IL-8 has consistently been shown to decrease with duration of lactation, regardless of gestational age. The results are inconsistent when compared across gestational ages. Ustundag and colleagues found no differences in the levels of IL-8 based on gestation , while Castellote and colleagues, as well as Mehta and Petrova, observed a lower amount of IL-8 measured in the colostrum from women who delivered prior to 30 weeks as compared to the colostrum obtained at later gestational ages [28•, 39•]. The decrease in IL-8 over the duration of lactation underscores the bioactive nature of human milk, which adjusts to the developing competence of the human immune system.
Similar to IL-6 and IL-8, IL-10 and TNF-α have been shown to vary based on gestational age at birth and duration of lactation. While the measurements of these cytokines are far lower when compared to IL-6 and IL-8, concentrations of IL-10 and TNF-α are highest in the milk of women who give birth between 30 and 37 weeks of gestation and lowest in women who give birth prior to 30 weeks of gestation [28•]. The high concentration of cytokines in colostrum when compared to more mature milk emphasizes the importance of early exposure to human milk as an essential component of the developing immune system during infancy, especially in the preterm infant.
Growth factors are among the important bioactive components found in human milk. Of particular importance to the preterm infant are epidermal growth factor (EGF) and transforming growth factor alpha and beta (TGF-α and TGF-β). These specific growth factors promote the functional development of the gastrointestinal mucosa beginning at birth, and when working together with antiinflammatory IL-10, they allow the immune system to tolerate antigens from nutritional exposures and specific microbiota found in the gut. In addition, these growth factors participate in the immune system to downregulate the inflammatory response and promote repair of damaged intestinal cells. The healing aspect of growth factors is of particular importance to preterm infants who may suffer intestinal injury including necrotizing enterocolitis (NEC).
Not unlike several other bioactive immune factors important to the preterm infant, EGF and TGF-α have been measured at higher concentrations in the milk of women who deliver preterm when compared to the milk of women who deliver at term [28•, 42]. In one study, where total protein concentrations did not vary based on gestational age at birth or in the first 7 days of lactation, both EGF and TGF-α were significantly higher during the first post-natal week in the milk of women who delivered very preterm (prior to 27 weeks of gestation) when compared with women who delivered between 32 and 36 weeks of gestation or between 38 and 42 weeks of gestation . Furthermore, this study showed that both of these growth factors were measured at the highest concentrations in the first week following birth and then tapered off gradually during the early neonatal period, but remained highest in the very preterm group even as the number of days of lactation increased. A more recent study with a similar design also showed that the EGF concentration in the milk of women who deliver before 30 weeks of gestation is higher than that of women who deliver later in pregnancy [28•]. The concentrations of TGF-β measured in this study were highest in the milk of women who delivered preterm (between 30 and 37 weeks), not in the very preterm group, who delivered before 30 weeks. The concentrations of TGF-β1 gradually decreased over time in all groups, with the highest concentrations measured in colostrum and the lowest concentrations measured in mature milk. This was slightly different for TGF-β2, where concentrations tapered less significantly from colostrum to mature milk and were slightly lower in the colostrum of the women who delivered very preterm [28•].
The high concentration of growth factors such as EGF measured in human milk, especially the milk of women who deliver preterm, very likely contributes to the protective effect of human milk for neonatal gastrointestinal diseases such as NEC. The unique importance of EGF to the immature gut is further supported by the fact that EGF receptors are found in both the fetal and neonatal intestine . Finally, the inverse relationship between EGF concentrations and gestational age support the speculation that growth factor content in human milk may be a maternal adaptation to premature delivery.
Lactoferrin, a prominent whey protein found in breast milk, is not only a prebiotic, but also antiinfective. Lactoferrin has been shown to reduce the production of inflammatory cytokines in monocytes and, in the presence of a probiotic (Lactobacillus GG), has enhanced defenses against infective enteric pathogens such as E. coli in the small intestines . In studies evaluating bioactive compounds in the breast milk of women who deliver preterm, lactoferrin has been shown to decrease over time, with higher levels observed during early lactation and lower levels observed by the end of the first month of lactation [38•]. When compared to the breast milk of women who deliver at term, lactoferrin has been measured at lower concentrations in the milk of women who deliver preterm [38•]. The higher concentration of lactoferrin in the milk of women who deliver at term might be explained by the need for higher concentrations of this protein in more mature infants, which serves as a growth factor for Bifidobacterium and Lactobacillus species.
Microbiology of Human Milk and Intestinal Colonization of the Preterm Infant
The implementation of advanced molecular approaches in the study of human microbiology and discoveries generated by the Human Microbiome Project have resulted in a renewed emphasis on the importance of microbial health [45–49]. While complex microbial-host relationships are understood to play a role in health and disease across the lifespan, never are they more important than during infancy, when the intestinal microbiome is first assembled . This assembly process is highly dependent on nutritional exposures during early infancy, where breast milk is likely to play a leading role as a result of the diversity of microbes that are present in this body fluid and due to the molecular mechanisms that are triggered by human milk oligosaccharides (HMO) found in breast milk, which act as a source of energy for desirable bacteria that are important to the establishment of an optimal microbiome.
The most recent metagenomic studies employing Illumina sequencing have shown that there is a highly diverse community of bacteria present in human milk samples [51•]. The population of bacteria found in the human milk samples included in this study was primarily aligned with the phyla of Proteobacteria (65 %) and Firmicutes (34 %) and the genera of Pseudomonas (61.1 %), Staphylococcus (34.4 %), and Streptococcus (0.5 %). Within these overall categories, 177 unique bacterial genera were measured in human milk samples. In another study involving 16S rRNA sequencing, stool samples obtained from breastfed infants were compared to those of formula-fed infants [52•]. In this study, breastfed infants had a higher proportion of Bacteroidetes and a lower proportion of Firmicutes and Verrucomicrobia when compared to formula-fed infants [52•]. The diversity of the bacterial communities found within human milk likely contributes to the overall intestinal colonization that occurs during infancy, but the exact mechanisms are not fully understood. The differences observed in this study may be explained by the microbial diversity found within the milk itself or by the presence of HMO within human milk (and lacking in infant formula) and, in turn, the intestinal microbiome of the breastfed infant who is colonized with health-promoting bacteria that are capable of metabolizing HMO.
Regardless of the mechanisms, studies using both Illumina and 16S rRNA sequencing have shown that the human milk microbiome, not unlike the microbiome found in other bodily habitats, is highly unique in its composition to each individual. The unique nature of the microbiome found in human milk is very likely influenced by the intestinal microbiome of the mother . It has been hypothesized that during the perinatal period, the permeability of the maternal gut allows for uptake of bacteria into the mother’s blood stream and then into the breast milk. Thus, the microbial population of the maternal gut has a potentially strong influence on the microbes found in breast milk and very likely contributes to the symbiotic effect of HMO on breast milk microbiota, which is ultimately an important part of infant nutrition and early intestinal colonization. In term infants, this process stimulates growth of Bifidobacteria, Lactobacillus, and Bacteroides, all of which have a protective effect on the newborn intestine. Unfortunately, the preterm infant does not benefit from this pattern of colonization, leaving the immature gut especially vulnerable . Further study of the microbiome characterizing human milk investigating the influence of the maternal gestation (i.e., term vs. preterm milk) and Holder pasteurization (65 °C for 5–30 min) commonly used by milk banks. This will enhance our understanding of the unique properties of human milk and the role that it plays in the intestinal colonization of the preterm infant.
Conclusion: Human Milk Exposure and Disease Prevention in the Preterm Infant
Children born preterm are characterized by an immature immune response and, as a result, are especially vulnerable to infectious and immune-mediated disease. As outlined in this article, human milk provides a unique composition of bioactive factors that have the ability to overcome the immature immune response and thus may prevent inflammatory diseases such as NEC in the short term, resulting in optimal growth and neurodevelopment in the long term.
NEC remains the most catastrophic gastrointestinal disease among preterm infants. The mechanisms underpinning NEC are multifactorial and remain poorly understood. The only consistently identified protective strategy against NEC is exposure to human milk [26, 55]. Preterm infants who are breast fed have been shown to be at a sixfold to tenfold lower risk of NEC when compared to formula-fed infants . The protective mechanisms provided by human milk against this disease are likely associated with optimal intestinal colonization, which helps to prevent against inflammation and infection by pathogenic bacteria. In addition, preterm infants fed with human milk have the advantage of an innate immune system that is programmed by the powerful immunological factors found in human milk. As a result, these children are better equipped to mount an appropriate inflammatory response that may prevent the disease pathogenesis common to NEC. In sum, providing human milk to preterm infants is of paramount importance to enhancing both short- and long-term health outcomes as a result of the unique immunologic properties found in this optimal source of infant nutrition.
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Conflict of Interest
Katherine E. Gregory declares that she has no conflict of interest. W. Allen Walker has received gifts from Mead Johnson Research and had travel/accommodation expenses covered or reiumbursed from Mead Johnson Research and Dannon Infant Nutrition.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.