What-is-colostrum
Colostrum is a specialized mammary secretion produced by mammals within the first 72 hours after parturition [1]. The term “colostrum” originates from Latin and originally referred to the first milk expressed from a cow following calving; however, this biological phenomenon is universal across all mammalian species [2]. Visually and physicochemically, colostrum differs markedly from mature milk. It typically appears as a thick, pale yellow liquid with a characteristic appearance due to its elevated concentrations of proteins, fat-soluble vitamins, and carotenoids [2]. Its consistency has been described as syrupy, and it exhibits a slightly salty, faintly metallic flavor resulting from its high levels of immunoglobulins and minerals. Depending on the species, diet, and individual variation, its color may range from light yellow to deep amber. The specific gravity of colostrum (1.045–1.060) is significantly higher than that of mature milk (1.028–1.033) [1].
The biological significance of colostrum lies in its role as a bridge between the protected intrauterine environment and the pathogen‑laden external world [1]. Unlike certain mammals—such as primates and rodents—that acquire maternal antibodies via transplacental transfer, many domestic livestock species, including cattle, horses, and pigs, rely entirely on immunoglobulins in colostrum to establish initial immune protection [3]. This process, known as passive transfer of immunity, constitutes a fundamental mechanism for the survival of neonates in these species. In species with epitheliochorial placentation, the placental barrier prevents the passage of maternal immunoglobulins to the fetus, leaving newborns wholly dependent on colostral antibodies for protection during the first few weeks after birth [3].
Immunoglobulin
IgG, IgA, IgM, IgD, IgE
Growth and repair factor
IGF, EGF, TGF, FGF, PDGF
Immunomodulatory factor
IL-1β, IL-6, TNF-α, IFN-γ
Broad-spectrum antibacterial factor
Lactoferrin, lysozyme, lactoperoxidase
Prebiotic oligosaccharides
3'SL, 6'SL, 6'SLN, DSL
The main constituents of colostrum include macronutrients (proteins, lipids, carbohydrates), micronutrients (vitamins, minerals), immune factors (immunoglobulins, lactoferrin, lysozyme), growth factors (insulin-like growth factor, epidermal growth factor, transforming growth factor), regulatory peptides (proline‑rich peptides, cytokines), and specialized bioactive molecules (oligosaccharides, nucleotides, hormones, etc.). Over the past century, methods for analyzing the composition of colostrum have continually evolved. Early biochemical studies identified the major protein fractions and established the dominant role of immunoglobulins among colostral proteins [4]. In the mid‑20th century, the advent of chromatographic and electrophoretic techniques enabled the separation and quantification of individual proteins, while modern proteomic, metabolomic, and glycomic approaches have revealed a molecular complexity far exceeding earlier estimates [5]. Today, mass‑spectrometry–based methods have identified more than 1,500 distinct proteins in bovine colostrum whey, with hundreds of additional peptides, lipids, and oligosaccharides now cataloged [5].
Macronutrients
Proteins and Peptides
Protein is the most abundant macronutrient class in colostrum and serves as the primary source of its bioactive functions. Bovine colostrum contains 14%–16% total protein, approximately 3–5 times the concentration found in mature milk [1][2]. The protein fraction comprises caseins, whey proteins, immunoglobulins, bioactive peptides, and numerous trace proteins with specialized functions.
Casein accounts for approximately 30%–40% of the total protein in the first milking of colostrum, forming a micellar structure that serves as a carrier for amino acids and minerals [6]. This proportion is markedly lower than that in mature milk, where casein comprises about 80%, owing to the exceptionally high immunoglobulin content in high‑quality colostrum—immunoglobulins belonging to the whey protein fraction—which shifts the casein-to-whey protein ratio in favor of whey proteins.
Whey protein accounts for approximately 60%–70% of the total protein in colostrum from the first milking, consistent with its high IgG content [6]. The major whey proteins include β‑lactoglobulin, α‑lactalbumin, bovine serum albumin, immunoglobulins, lactoferrin, and lysozyme [6][7]. In addition to their nutritional value, many whey proteins exhibit bioactive properties, some of which are activated only upon acidification or partial digestion. Proteomic analyses have identified more than 200 distinct whey proteins in bovine colostrum, many of which are present at trace levels yet possess potent biological activities [5].
Endogenous peptides: Colostrum contains a pool of endogenous peptides generated through limited proteolysis of maternal proteins. These peptides typically range from 5 to 50 amino acids in length and exhibit diverse biological activities. Studies have identified thousands of endogenous peptides in bovine colostrum, many of which are differentially expressed between colostrum and mature milk [5].
Lipids and Fatty Acids
Colostrum contains 6%–8% fat, providing a concentrated source of energy and essential fatty acids [2]. Its lipid composition comprises triglycerides (95%–98%), phospholipids (0.5%–1%), cholesterol (0.2%–0.5%), as well as trace components such as fat-soluble vitamins and carotenoids. The fatty acid profile of colostrum differs from that of mature milk, with a higher proportion of saturated fatty acids and a distinctive pattern of polyunsaturated fatty acids [2]. Colostrum is particularly rich in medium-chain fatty acids—caprylic acid (C8:0) and capric acid (C10:0)—which are rapidly absorbed and metabolized, supplying immediate energy to the neonate. The phospholipid fraction is concentrated in the milk fat globule membrane (MFGM), which contains bioactive phospholipids such as sphingomyelin, phosphatidylcholine, and phosphatidylethanolamine [6].
Carbohydrates
Colostrum contains 2.5%–3.5% lactose, significantly lower than that of mature milk (4.5%–5.0%) [1]. This relatively low lactose content may reflect the limited lactase activity immediately after birth in neonates, as well as the prioritization of immune functions over purely nutritional ones during this critical window. Lactose also serves as a primer for oligosaccharide synthesis in the mammary gland and as a reducing-end substrate for glycosyltransferases. Bovine colostrum contains 1–2 g/L of oligosaccharides, representing a 5–10-fold enrichment compared with mature milk [8]. At least 40 distinct oligosaccharides have been identified in bovine colostrum, categorized into neutral and acidic (sialylated) types. Sialylated oligosaccharides predominate, accounting for more than 70% of the total oligosaccharides in colostrum. Human colostrum is particularly rich in oligosaccharides, with concentrations of 22–24 g/L, whereas bovine colostrum contains approximately 1 g/L [6]. To date, over 200 different oligosaccharides have been characterized in human milk, a diversity far exceeding that of bovine colostrum [8].
Immune factor
Immunoglobulin
Immunoglobulins are the most abundant class of proteins in bovine colostrum, with total IgG concentrations in first-milk colostrum reaching 30–100 mg/mL—approximately 50–100 times higher than in mature milk [1][4].
Immunoglobulin G (IgG): IgG is the predominant immunoglobulin in bovine colostrum, accounting for approximately 85%–90% of the total immunoglobulins. In high-quality first-milk colostrum, it comprises about 70%–80% of the total colostral protein, declining to 50%–60% by 24 hours postpartum [1]. Bovine IgG exists in three subclasses: IgG1 (the most abundant, representing 80%–85% of colostral IgG), IgG2 (10%–15%), and IgG3 (present at very low concentrations). The IgG molecule has a molecular weight of approximately 150 kDa and contains two antigen-binding sites (Fab regions) as well as an Fc region that mediates complement activation, opsonization, and binding to Fc receptors on immune cells [4].
Immunoglobulin A (IgA) in colostrum is predominantly present as secretory IgA (sIgA), a dimeric form bound to the J chain and the secretory component. The concentration of colostral IgA ranges from 1 to 5 mg/mL, approximately 10–25 times that of mature milk. Unlike IgG, which is transported from the bloodstream, IgA is locally synthesized by plasma cells in the mammary gland under the influence of the gut–mammary immune axis [6]. Immunoglobulin M (IgM) in colostrum exists as a pentameric molecule (with a molecular weight of about 900 kDa) and exhibits high multivalent antigen-binding capacity. The concentration of colostral IgM is 1–5 mg/mL. Immunoglobulin D (IgD) is present in colostrum at low concentrations and works closely with IgM to activate B cells [9].
Lactoferrin
Lactoferrin is an iron‑binding glycoprotein belonging to the transferrin family, with a molecular mass of approximately 80 kDa [6]. Bovine colostrum contains 1–5 g/L of lactoferrin, while its concentration in mature milk decreases to 0.02–0.35 g/L. In human colostrum, the lactoferrin concentration ranges from 3 to 7 mg/mL, roughly 2–5 times higher than that in typical bovine colostrum, though considerable inter‑individual variability exists [7]. Lactoferrin consists of a single polypeptide chain folded into two homologous lobes (N‑lobe and C‑lobe), each capable of binding a trivalent iron ion with very high affinity. The protein can exist in either apo‑lactoferrin (iron‑free) or holo‑lactoferrin (iron‑saturated) forms. The glycosylation pattern of lactoferrin influences its stability, resistance to proteolysis, and receptor binding.
Lysozyme
Lysozyme is a 14 kDa enzyme that hydrolyzes the β-(1,4) glycosidic bonds in bacterial peptidoglycans. The concentration of lysozyme in colostrum is approximately 2–10 times that in mature milk (about 0.14–0.7 mg/L in colostrum versus 0.07–0.6 mg/L in mature milk) [7].
Lactoperoxidase
Lactoperoxidase is a heme-containing enzyme that catalyzes the oxidation of thiocyanate by hydrogen peroxide, yielding hypothiocyanite. The lactoperoxidase system constitutes an important non‑immunoglobulin–mediated immune defense mechanism in colostrum and milk.
Complement proteins
Colostrum contains complement components, including C3, C4, and factor B. The concentrations of these complement proteins in colostrum are significantly higher than in mature milk, reflecting the prioritization of immune defense during the neonatal period.
Growth factor
Insulin-like growth factor (IGF) is one of the most abundant growth factors in colostrum. Bovine colostrum contains 300–500 ng/mL of IGF‑1 and 200–400 ng/mL of IGF‑2, at concentrations 10–100 times higher than those in mature milk [7]. IGFs are polypeptides with structural homology to insulin. There is 100% sequence identity between bovine and human IGFs [7]. IGF‑1 is the predominant growth factor in colostrum. In colostrum, IGF is protected from proteolytic degradation through its association with IGF‑binding proteins (IGFBPs). In addition, colostrum also contains other growth factors, such as epidermal growth factor (EGF), transforming growth factor‑β (TGF‑β), and transforming growth factor‑α (TGF‑α).
Regulatory peptides and cytokines
Proline-Rich Polypeptide (PRP)
Proline‑Rich Polypeptides (PRP), also known as colostrinin, are a complex of peptides with molecular weights ranging from 500 to 3,000 Da [11]. Initially isolated from sheep colostrum, PRP has since been identified in bovine colostrum as well. The PRP complex contains approximately 25% proline and 40% hydrophobic amino acids; this unusual compositional profile contributes to its structural stability and biological activity [11].
Cytokine
Colostrum contains a variety of cytokines. The concentrations of cytokines in colostrum are significantly higher than those in mature milk. Both pro-inflammatory cytokines (IL‑1β, IL‑6, TNF‑α, IFN‑γ) and anti-inflammatory cytokines (IL‑10, TGF‑β, IL‑1Ra) are present.
Other Bioactive Factors
01
Nucleotides and Nucleosides
Colostrum contains nucleotides and nucleosides. Uridine and uridine 5′-monophosphate are the most abundant nucleosides and nucleotides in colostrum. The concentration of nucleotides in colostrum peaks 24–48 hours postpartum and then gradually declines.
02
microRNA
Recent studies have revealed that colostrum contains microRNAs (miRNAs) [12]. Colostrum harbors a higher concentration of miRNAs than mature milk. Key immune‑related miRNAs identified in bovine colostrum include miR‑142‑5p, miR‑150, miR‑155, miR‑181a, and miR‑223 [14].
03
Ganglioside
Gangliosides are polar glycosphingolipids found in the milk fat globule membrane and participate in a variety of biological functions [15]. The concentration of gangliosides in colostrum is higher than in mature milk, reflecting their critical role in the development of the neonate.
Trypsin inhibitors and protease inhibitors
Bovine colostrum contains trypsin inhibitor, a protein that protects immunoglobulin G (IgG), growth factors, and other bioactive proteins from proteolytic degradation in the gastrointestinal tract [10]. The concentration of trypsin inhibitor in bovine colostrum is approximately 5–15 times higher than in mature milk [10]. Studies have shown that the concurrent presence of casein partially shields epidermal growth factor from digestion, while the protease‑inhibitory profile of colostrum further enhances the stability and absorption of IGF‑1 [7]. In addition to trypsin inhibitor, colostrum also contains α1‑antitrypsin, α2‑macroglobulin, and other serine protease inhibitors (serpins), which together form a protease‑inhibition network [1].
References
[1] Silva FG, Silva SR, Pereira AMF, Cerqueira JL, Conceição C. A Comprehensive Review of Bovine Colostrum Components and Selected Aspects Regarding Their Impact on Neonatal Calf Physiology. Animals. 2024;14(7):1130.
[2] McGrath BA, Fox PF, McSweeney PLH, Kelly AL. Composition and properties of bovine colostrum: a review. Dairy Sci Technol. 2016;96(2):133-158.
[3] Langer P. Differences in the composition of colostrum and milk in eutherians reflect differences in immunoglobulin transfer. J Mammal. 2009;90(2):332-339.
[4] Hurley WL, Theil PK. Perspectives on immunoglobulins in colostrum and milk. Nutrients. 2011;3(4):442-474.
[5] Zhang L, et al. Unravelling the proteomic profiles of bovine colostrum and mature milk derived from the first and second lactations. Food Res Int. 2023;173:112589.
[6] Canbolat AA, Lombardo M, Mondragon AC, Miranda JML, Bechelany M. Bovine Colostrum in Pediatric Nutrition and Health. Nutrients. 2024;16(24):4305.
[7] Playford RJ, Weiser MJ. Bovine Colostrum: Its Constituents and Uses. Nutrients. 2021;13(1):265.
[8] Smilowitz JT, Lebrilla CB, Mills DA, German JB, Freeman SL. Breast Milk Oligosaccharides: Structure-Function Relationships in the Neonate. Annu Rev Nutr. 2014;34:143-169.
[9] Pier GB, Lyczak JB, Wetzler LM. Immunology, Infection, and Immunity. ASM Press; 2004.
[10] Quigley JD 3rd, Martin KR, Dowlen HH. Concentrations of trypsin inhibitor and immunoglobulins in colostrum of Jersey cows. J Dairy Sci. 1995;78(7):1573-1577.
[11] Janusz M, Zabłocka A. Proline-rich polypeptide (PRP) from ovine colostrum: colostrinin with immunomodulatory activity. Arch Immunol Ther Exp. 1993;41(5-6):427-438.
[12] Puppel K, Gołębiewski M, Grodkowski G, et al. Composition and factors affecting quality of bovine colostrum: A review. Animals. 2019;9(12):1070.
[13] Van Hese I, Goossens K, Vandaele L, Opsomer G. Invited review: MicroRNAs in bovine colostrum—Focus on their origin and potential health benefits for the calf. J Dairy Sci. 2020;103(1):1-15.
[14] Hue DT, Hatazoe H, Kameyama K, et al. Analysis of immune-related microRNAs in cows and newborn calves. J Dairy Sci. 2023;106(4):2866-2878.
[15] Xu J, Niu X, Yin M, et al. Dietary GD3 ganglioside reduces the incidence and severity of necrotizing enterocolitis by sustaining regulatory immune responses. J Pediatr Gastroenterol Nutr. 2013;57(5):607-614.
[16] Bielmann V, Gillan J, Perkins NR, et al. Comparison of Brix refractometry to digital refractometry for the assessment of colostrum quality in dairy cattle. J Dairy Sci. 2014;97(9):5398-5404.
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