Cord blood group 2 innate lymphoid cells are associated with lung function at 6 weeks of age

Gabriela Martins Costa Gomes1, Patricia de Gouveia Belinelo1, Malcolm R Starkey1,2,3

  • 1Priority Research Centre GrowUpWell® - Hunter Medical Research Institute The University of Newcastle Newcastle NSW Australia.

Insights

Infant lung function is linked to fetal immune cells. Higher levels of fetal group 2 innate lymphoid cells (ILC2) in cord blood correlate with poorer lung function in newborns born to mothers with asthma.

Area of Science:

  • Immunology
  • Neonatal Health
  • Respiratory Medicine

Background:

  • Maternal asthma during pregnancy is associated with reduced offspring lung function.
  • Human fetal lungs exhibit a 10-fold higher accumulation of group 2 innate lymphoid cells (ILC2) compared to adult lungs.
  • Limited data exists on fetal ILC2 levels and their impact on early-life respiratory health.

Purpose of the Study:

  • To investigate cord blood immune cell populations in infants born to mothers with asthma.
  • To explore the association between fetal ILC2 numbers and infant lung function.

Main Methods:

  • Cord blood samples were collected from infants of asthmatic mothers.
  • Immune cells were analyzed using traditional gating and computational methods (t-SNE, PhenoGraph).
  • Infant lung function was assessed at 6 weeks using tPTEF/tE% and Lung Clearance Index (LCI).

Main Results:

  • 91 out of 110 infants were immunophenotyped.
  • Lung function measurements were obtained from 43 (tPTEF/tE%) and 34 (LCI) infants.
  • Increased fetal ILC2 numbers, specifically with CRTh2 expression, were associated with poorer infant lung function at 6 weeks.

Conclusions:

  • Fetal immune responses, particularly ILC2 levels, may influence or predict early-life lung function outcomes.
  • This suggests a potential link between the fetal immune environment and respiratory health trajectory.
Abstract

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...
533
Primary Lymphoid Organs01:16

Primary Lymphoid Organs

Primary lymphoid organs are pivotal in the formation, development, and maturation of lymphocytes, the white blood cells that serve as the backbone of our immune system. This crucial function underscores their fundamental role in maintaining our overall health and immunity. The two primary lymphoid organs of prime importance are the red bone marrow and the thymus.
The red bone marrow is a soft, spongy tissue nestled in the interior of long bones such as the humerus and femur. It is the site...
12.1K
Secondary Lymphoid Organs01:15

Secondary Lymphoid Organs

Secondary organs, including lymph nodes, the spleen, and mucosa-associated lymphoid tissue (MALT), work harmoniously to protect us from disease and infection.
The spleen is a vital organ in the lymphatic system, nestled in the upper left side of the abdomen. It is composed of two primary regions: the red pulp and the white pulp, each having distinct functions. The red pulp performs a significant role in blood filtration. It efficiently purges the blood of old or damaged red blood cells and...
7.2K
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...
6.6K