Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Apr;30(2):111-123.
doi: 10.1293/tox.2016-0075. Epub 2016 Dec 24.

The lymphoid system: a review of species differences

Affiliations
Review

The lymphoid system: a review of species differences

Patrick J Haley. J Toxicol Pathol. 2017 Apr.

Abstract

While an understanding of the structure and function of a generically described immune system is essential in contemporary biomedicine, it is clear that a one-size-fits-all approach applied across multiple species is fraught with contradictions and inconsistencies. Nevertheless, the breakthroughs achieved in immunology following the application of observations in murine systems to that of man have been pivotal in the advancement of biology and human medicine. However, as additional species have been used to further address biologic and safety assessment questions relative to the structure and function of the immune system, it has become clear that there are differences across species, gender, age and strain that must be considered. The meaningfulness of these differences must be determined on a case-by-case basis. This review article attempts to collect, consolidate and discuss some of these species differences thereby aiding in the accurate placement of new observations in a proper immunobiological and immunopathological perspective.

Keywords: immunobiology; immunology; immunopathology; lymphoid function; lymphoid system; species differences.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Rat spleen. A: white pulp (PAS); B: primary folliculo-nodule; C: secondary folliculo-nodule; D: marginal zone; E: central arteriole; F: thin capsule; G red pulp; H: thin trabeculae.
Fig. 2.
Fig. 2.
Dog spleen. A: white pulp (PAS); B: primary folliculo-nodule; C: secondary folliculo-nodule; D: marginal zone; E: central arteriole; F: thick capsule; G red pulp; H: thick trabeculae.
Fig. 3.
Fig. 3.
Rat lymph node. 1: Cortex; A: peripheral cortex; B: primary folliculo-nodule; C: secondary folliculo-nodule; D: germinal center; E: deep cortical unit; 2: Medulla; F: medullary cord; G: medullary sinus; H: septum.
Fig. 4.
Fig. 4.
Dog lymph node. 1: Cortex; A: primary folliculo-nodule; B: secondary folliculo-nodule with germinal center; C: mantle; D: deep cortical unit; 2: Medulla; E: medullary cord; F: medullary sinus; G: septum.
Fig. 5.
Fig. 5.
Pig lymph node. Note reversal of location of cortex and medulla.

References

    1. Dean JH. Special issue on Immunotoxicology. Drug Chem Toxicol. 2: 1–179. 1979.
    1. Dean JH, Hincks JR, and Remandet B. Immunotoxicology assessment in the pharmaceutical industry. Toxicol Lett. 102-103: 247–255. 1998. - PubMed
    1. Luster MI, Munson AE, Thomas PT, Holsapple MP, Fenters JD, White KL, Jr , Lauer LD, Germolec DR, Rosenthal GJ, and Dean JH. Development of a testing battery to assess chemical-induced immunotoxicity: National Toxicology Program’s guidelines for immunotoxicity evaluation in mice. Fundam Appl Toxicol. 10: 2–19. 1988. - PubMed
    1. ICH (International Conference on Harmonization). Guidance for Industry. S8 Immunotoxicity Studies for Human Pharmaceuticals. 2006, from U.S. Food & Drug Administration website: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformati....
    1. Maronpot RR. A monograph on histomorphologic evaluation of lymphoid organs. Toxicol Pathol. 34: 407–408. 2006. - PubMed

LinkOut - more resources