Natural Microbial Exposure from the Earliest Natural Time Point Enhances Immune Development by Expanding Immune Cell Progenitors and Mature Immune Cells

Author:

Burger Sarah12,Stenger Terran13ORCID,Pierson Mark13,Sridhar Adhvaith12,Huggins Matthew A.13,Kucaba Tamara A.4,Griffith Thomas S.14567ORCID,Hamilton Sara E.1356ORCID,Schuldt Nathaniel J.126ORCID

Affiliation:

1. *Center for Immunology, University of Minnesota, Minneapolis, MN

2. †Department of Pediatrics, University of Minnesota, Minneapolis, MN

3. ‡Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN

4. §Department of Urology, University of Minnesota, Minneapolis, MN

5. ¶Microbiology, Immunology, and Cancer Biology PhD Program, University of Minnesota, Minneapolis, MN

6. ‖Masonic Cancer Center, University of Minnesota, Minneapolis, MN

7. #Minneapolis VA Health Care System, Minneapolis, MN

Abstract

Abstract Microbial experience fundamentally shapes immunity, particularly during the perinatal period when the immune system is underdeveloped, and novel microbial encounters are common. Most animal models are raised in specific pathogen-free (SPF) conditions with relatively uniform microbial communities. How SPF housing conditions alter early-life immune development relative to natural microbial exposure (NME) has not been thoroughly investigated. In this article, we compare immune development in SPF-raised mice with mice born from immunologically experienced mothers in microbially diverse environments. NME induced broad immune cell expansion, including naive cells, suggesting mechanisms besides activation-induced proliferation contribute to the increase in immune cell numbers. We found NME conditions also expanded immune cell progenitor cell populations in the bone marrow, suggesting microbial experience enhances immune development at the earliest stages of immune cell differentiation. Multiple immune functions characteristically impaired in infants were also enhanced by NME, including T cell memory and Th1 polarization, B cell class switching and Ab production, proinflammatory cytokine expression, and bacterial clearance after Listeria monocytogenes challenge. Collectively, our studies reveal numerous impairments in immune development in SPF conditions relative to natural immune development.

Funder

HHS | NIH | National Institute of General Medical Sciences

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

University of Minnesota, Department of Pediatrics

University of Minnesota

U.S. Department of Veterans Affairs

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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