Development of immune organs and functioning in humans and test animals: Implications for immune intervention studies

Reprod Toxicol. 2016 Sep:64:180-90. doi: 10.1016/j.reprotox.2016.06.002. Epub 2016 Jun 6.

Abstract

A healthy immune status is mostly determined during early life stages and many immune-related diseases may find their origin in utero and the first years of life. Therefore, immune health optimization may be most effective during early life. This review is an inventory of immune organ maturation events in relation to developmental timeframes in minipig, rat, mouse and human. It is concluded that time windows of immune organ development in rodents can be translated to human, but minipig reflects the human timeframes better; however the lack of prenatal maternal-fetal immune interaction in minipig may cause less responsiveness to prenatal intervention. It is too early to conclude which immune parameters are most appropriate, because there are not enough comparative immune parameters. Filling these gaps will increase the predictability of results observed in experimental animals, and guide future intervention studies by assessing relevant parameters in the right corresponding developmental time frames.

Keywords: Critical windows; Hematopoiesis; Immune system development; Liver; Lymph nodes; MALT; Species comparison; Spleen; Thymus.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / immunology*
  • Animals
  • Embryonic Development / immunology*
  • Fetal Development / immunology*
  • Hematopoiesis / immunology*
  • Humans
  • Lymphoid Tissue* / embryology
  • Lymphoid Tissue* / growth & development
  • Lymphoid Tissue* / immunology
  • Species Specificity