AUTHOR=Conley Haleigh E. , He Max M. , Easterhoff David , Kirshner Hélène Fradin , Cocklin Sarah L. , Meyer Jacob , Hoxie Taylor , Berry Madison , Bradley Todd , Tolbert William D. , Pazgier Marzena , Tomaras Georgia D. , Schmitz Joern E. , Moody Michael Anthony , Wiehe Kevin , Pollara Justin TITLE=Defining genetic diversity of rhesus macaque Fcγ receptors with long-read RNA sequencing JOURNAL=Frontiers in Immunology VOLUME=14 YEAR=2024 URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1306292 DOI=10.3389/fimmu.2023.1306292 ISSN=1664-3224 ABSTRACT=
Fcγ receptors (FcγRs) are membrane-bound glycoproteins that bind to the fragment crystallizable (Fc) constant regions of IgG antibodies. Interactions between IgG immune complexes and FcγRs can initiate signal transduction that mediates important components of the immune response including activation of immune cells for clearance of opsonized pathogens or infected host cells. In humans, many studies have identified associations between FcγR gene polymorphisms and risk of infection, or progression of disease, suggesting a gene-level impact on FcγR-dependent immune responses. Rhesus macaques are an important translational model for most human health interventions, yet little is known about the breadth of rhesus macaque FcγR genetic diversity. This lack of knowledge prevents evaluation of the impact of FcγR polymorphisms on outcomes of preclinical studies performed in rhesus macaques. In this study we used long-read RNA sequencing to define the genetic diversity of FcγRs in 206 Indian-origin Rhesus macaques,