Leukocyte Populations in Human Preterm and Term Breast Milk Identified by Multicolour Flow Cytometry

PLoS One. 2015 Aug 19;10(8):e0135580. doi: 10.1371/journal.pone.0135580. eCollection 2015.

Abstract

Background: Extremely preterm infants are highly susceptible to bacterial infections but breast milk provides some protection. It is unknown if leukocyte numbers and subsets in milk differ between term and preterm breast milk. This study serially characterised leukocyte populations in breast milk of mothers of preterm and term infants using multicolour flow cytometry methods for extended differential leukocyte counts in blood.

Methods: Sixty mothers of extremely preterm (<28 weeks gestational age), very preterm (28-31 wk), and moderately preterm (32-36 wk), as well as term (37-41 wk) infants were recruited. Colostrum (d2-5), transitional (d8-12) and mature milk (d26-30) samples were collected, cells isolated, and leukocyte subsets analysed using flow cytometry.

Results: The major CD45+ leukocyte populations circulating in blood were also detectable in breast milk but at different frequencies. Progression of lactation was associated with decreasing CD45+ leukocyte concentration, as well as increases in the relative frequencies of neutrophils and immature granulocytes, and decreases in the relative frequencies of eosinophils, myeloid and B cell precursors, and CD16- monocytes. No differences were observed between preterm and term breast milk in leukocyte concentration, though minor differences between preterm groups in some leukocyte frequencies were observed.

Conclusions: Flow cytometry is a useful tool to identify and quantify leukocyte subsets in breast milk. The stage of lactation is associated with major changes in milk leukocyte composition in this population. Fresh preterm breast milk is not deficient in leukocytes, but shorter gestation may be associated with minor differences in leukocyte subset frequencies in preterm compared to term breast milk.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Breast Feeding
  • Colostrum / cytology*
  • Eosinophils / cytology
  • Female
  • Flow Cytometry
  • Gestational Age
  • Granulocytes / cytology
  • Humans
  • Infant, Premature / immunology*
  • Lactation
  • Leukocyte Common Antigens / metabolism
  • Leukocyte Count*
  • Leukocytes / cytology*
  • Milk, Human / cytology*
  • Myeloid Cells / cytology
  • Neutrophils / cytology
  • Pregnancy
  • Premature Birth
  • Term Birth

Substances

  • Leukocyte Common Antigens

Grants and funding

ST received postgraduate scholarships from the Centre for Neonatal Research and Education, Women and Infants Research Foundation (WIRF), and the Princess Margaret Hospital (PMH) foundation. TS and ST received an early career grant from WIRF for this work. FH was the recipient of an unrestricted research grant by Medela AG (Switzerland). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.