A Novel Organized Nasopharynx-Associated Lymphoid Tissue in Teleosts That Expresses Molecular Markers Characteristic of Mammalian Germinal Centers

Author:

Garcia Benjamin1ORCID,Dong Fen12ORCID,Casadei Elisa1,Rességuier Julien3ORCID,Ma Jie4ORCID,Cain Kenneth D.4,Castrillo Pedro A.15ORCID,Xu Zhen2,Salinas Irene1

Affiliation:

1. *Department of Biology, Center for Evolutionary and Theoretical Immunology, University of New Mexico, Albuquerque, NM;

2. †Department of Aquatic Animal Medicine, College of Fisheries, Huazhong Agricultural University, China;

3. ‡Section for Physiology and Cell Biology, Department of Biosciences, University of Oslo, Oslo, Norway;

4. §Department of Fish and Wildlife Sciences, University of Idaho, Moscow, ID; and

5. ¶Departamento de Anatomía, Producción Animal y Ciencias Clínicas Veterinarias, Universidade de Santiago de Compostela, Santiago de Compostela, Spain

Abstract

Abstract Nasal immunity is an ancient and conserved arm of the mucosal immune system in vertebrates. In teleost fish, we previously reported the presence of a nasopharynx-associated lymphoid tissue (NALT) characterized by scattered immune cells located in the trout olfactory lamellae. This diffuse NALT mounts innate and adaptive immune responses to nasal infection or vaccination. In mammals, lymphoid structures such as adenoids and tonsils support affinity maturation of the adaptive immune response in the nasopharyngeal cavity. These structures, known as organized NALT (O-NALT), have not been identified in teleost fish to date, but their evolutionary forerunners exist in sarcopterygian fish. In this study, we report that the rainbow trout nasal cavity is lined with a lymphoepithelium that extends from the most dorsal opening of the nares to the ventral nasal cavity. Within the nasal lymphoepithelium we found lymphocyte aggregates called O-NALT in this study that are composed of ∼ 56% CD4+, 24% IgM+, 16% CD8α+, and 4% IgT+ lymphocytes and that have high constitutive aicda mRNA expression. Intranasal (i.n.) vaccination with live attenuated infectious hematopoietic necrosis virus triggers expansions of B and T cells and aicda expression in response to primary i.n. vaccination. IgM+ B cells undergo proliferation and apoptosis within O-NALT upon prime but not boost i.n. vaccination. Our results suggest that novel mucosal microenvironments such as O-NALT may be involved in the affinity maturation of the adaptive immune response in early vertebrates.

Funder

USDA | National Institute of Food and Agriculture

National Natural Science Foundation of China

China Scholarship Council

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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