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IgG Binding Characteristics of Rhesus Macaque FcγR.
Chan, Ying N; Boesch, Austin W; Osei-Owusu, Nana Y; Emileh, Ali; Crowley, Andrew R; Cocklin, Sarah L; Finstad, Samantha L; Linde, Caitlyn H; Howell, Rebecca A; Zentner, Isaac; Cocklin, Simon; Miles, Adam R; Eckman, Joshua W; Alter, Galit; Schmitz, Joern E; Ackerman, Margaret E.
Afiliación
  • Chan YN; Thayer School of Engineering, Dartmouth College, Hanover, NH 03755;
  • Boesch AW; Thayer School of Engineering, Dartmouth College, Hanover, NH 03755;
  • Osei-Owusu NY; Molecular and Cellular Biology Program, Dartmouth College, Hanover, NH 03755;
  • Emileh A; Thayer School of Engineering, Dartmouth College, Hanover, NH 03755;
  • Crowley AR; Molecular and Cellular Biology Program, Dartmouth College, Hanover, NH 03755;
  • Cocklin SL; Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;
  • Finstad SL; Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;
  • Linde CH; Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;
  • Howell RA; Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;
  • Zentner I; Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102;
  • Cocklin S; Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102;
  • Miles AR; Wasatch Microfluidics, Salt Lake City, UT 84103; and.
  • Eckman JW; Wasatch Microfluidics, Salt Lake City, UT 84103; and.
  • Alter G; Ragon Institute of MGH, MIT and Harvard, Cambridge, MA 02139.
  • Schmitz JE; Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;
  • Ackerman ME; Thayer School of Engineering, Dartmouth College, Hanover, NH 03755; Molecular and Cellular Biology Program, Dartmouth College, Hanover, NH 03755; margaret.e.ackerman@dartmouth.edu.
J Immunol ; 197(7): 2936-47, 2016 10 01.
Article en En | MEDLINE | ID: mdl-27559046
ABSTRACT
Indian rhesus macaques (Macaca mulatta) are routinely used in preclinical studies to evaluate therapeutic Abs and candidate vaccines. The efficacy of these interventions in many cases is known to rely heavily on the ability of Abs to interact with a set of Ab FcγR expressed on innate immune cells. Yet, despite their presumed functional importance, M. mulatta Ab receptors are largely uncharacterized, posing a fundamental limit to ensuring accurate interpretation and translation of results from studies in this model. In this article, we describe the binding characteristics of the most prevalent allotypic variants of M. mulatta FcγR for binding to both human and M. mulatta IgG of varying subclasses. The resulting determination of the affinity, specificity, and glycan sensitivity of these receptors promises to be useful in designing and evaluating studies of candidate vaccines and therapeutic Abs in this key animal model and exposes significant evolutionary divergence between humans and macaques.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoglobulina G / Receptores Fc Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoglobulina G / Receptores Fc Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2016 Tipo del documento: Article