Formula feeding skews immune cell composition toward adaptive immunity compared to breastfeeding

Yvonne Andersson1, Marie-Louise Hammarström, Bo Lönnerdal

  • 1Department of Clinical Sciences, Pediatrics, Umeå University, Umeå SE-901 87, Sweden.

Insights

Infant feeding impacts immune cell development. Breastfeeding promotes steady immune cell composition, while formula feeding may delay innate immunity cell recruitment and enhance adaptive immunity cell maturation.

Area of Science:

  • Immunology
  • Pediatrics
  • Nutrition

Background:

  • The ontogeny of infant immune systems and the influence of feeding type remain incompletely understood.
  • Early life nutrition significantly shapes immune system development and function.

Purpose of the Study:

  • To analyze immune cell frequencies and composition in breastfed (BF) versus formula-fed (FF) infants.
  • To compare the effects of different infant formulas on immune cell development.

Main Methods:

  • Flow cytometry and immunoflow cytometry were used to analyze whole blood and peripheral blood mononuclear cells (PBMCs).
  • Immune cell populations were assessed in exclusively BF infants and infants fed one of three different formulas at 1.5, 4, and 6 months of age.

Main Results:

  • Breastfed infants showed increased neutrophils and stable lymphocyte proportions (CD4+ T cells, CD8+ T cells, B cells, NK cells, gammadelta T cells) from 1.5 to 6 months.
  • Formula-fed infants had a decreased proportion of NK cells but increased naive CD4+ T cells and an elevated CD4/CD8 ratio compared to breastfed infants.
  • No significant differences in immune cell composition were observed among the three formula groups.

Conclusions:

  • Infant feeding type significantly influences immune cell ontogeny.
  • Formula feeding is associated with delayed recruitment of innate immunity cells (NK cells) and accelerated maturation of adaptive immunity cells (naive CD4+ T cells) compared to breastfeeding.

Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from the skin...
Introduction to Innate and Adaptive Immunity01:21

Introduction to Innate and Adaptive Immunity

The human immune system is a complex defense mechanism that protects the body from harmful pathogens and foreign substances. It comprises two crucial components: innate and adaptive immunity.
Innate immunity is the body's natural, nonspecific defense system that acts quickly to protect against pathogens. It incorporates physical barriers like skin and mucous membranes and cellular elements such as phagocytes and natural killer cells. This part of our immune system provides an immediate,...
Special Features of Adaptive Immunity01:20

Special Features of Adaptive Immunity

The adaptive immune system, a crucial component of the overall immune response, offers a highly specialized defense against pathogens. It involves specific cell types and features, enabling it to combat infections effectively and efficiently.
The primary cell types involved in adaptive immunity are T cells and B cells. Each type has a unique role in defending the body against pathogens. T cells are responsible for cell-mediated immunity. They identify and eliminate infected cells directly,...
Cell-mediated Immune Responses01:40

Cell-mediated Immune Responses

Overview
Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...