bioRxivImmunology
Comparative analysis of cellular immune responses in conventional and SPF Baboons (Papio spp.)
E. R. Magden, B. P. Nehete, S. Chitta, L. E. Williams, J. H. Simmons, C. R. Abee, P. N. Nehete
Abstract
Baboons (papio spp.) have served as a successful model of human disease such as cardiac and respiratory, infectious, diabetes, genetics, immunology, aging, and xenotransplantation. The development of an immunologically defined specific-pathogen free (SPF) baboon model has further advanced research, especially with studies involving the immune system and immunosuppression. In this study, we compare normal immunological changes of peripheral blood mononuclear cell (PBMC) subsets, and their function in age-matched conventional and SPF baboons. Our results demonstrate that both groups have comparable numbers of different lymphocyte subsets, but there are phenotypic differences in central and effector memory T cells subsets that are more pronounced in the CD4+ T cells. Despite equal proportions of CD3+ T cells among the conventional and SPF baboon groups, PBMC show higher proliferative responses to mitogens PHA and PWM and higher IFN-{gamma} producing cells to Con A and PWM in the conventional group. Plasma levels of the inflammatory cytokine TNF- were significantly higher in SPF baboons. Exposure of PBMC from conventional baboons to various Toll like ligands (TLR ligands) TLR-3, TLR-4 and TLR-8 show higher IFN-{gamma} producing cells while PBMC from SPF baboons stimulated with TLR-5 and TLR-6 ligand show higher IFN-{gamma} producing cells. These findings suggest that while the lymphocyte subsets in conventional and SPF baboons share many phenotypic and functional similarities, specific differences exist in immune function of lymphocytes which could impact the quality and quantity of innate and adaptive immune responses. These differences should be considered for better experimental outcomes, specifically in studies measuring immunological endpoints.
- organism: non-human primate
- assay: proteomics
- assay: flow cytometry
- research focus: cell type annotation
- research focus: differential expression
- research focus: cell-cell communication
- approach: experimental assay
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