Biburger M, Aschermann S, Schwab I, Lux A, Albert H, Danzer H, Woigk M, Dudziak D, Nimmerjahn F (2011)
Publication Status: Published
Publication Type: Journal article, Original article
Publication year: 2011
Publisher: Elsevier (Cell Press)
Book Volume: 35
Pages Range: 932-944
Journal Issue: 6
DOI: 10.1016/j.immuni.2011.11.009
Immunoglobulin G (IgG) antibodies confer protection against pathogenic microorganisms, serve as therapeutics in tumor therapy, and are involved in destruction of healthy tissues during autoimmune diseases. Understanding the molecular pathways and effector cell types involved in antibody-mediated effector functions is a prerequisite to modulate these activities. In this study we used two independent model systems to identify innate immune effector cells required for IgG activity in vivo. We first defined the precise repertoire of receptors for the IgG Fc fragment (FcγR) on innate immune effector cells in the blood and on tissue-resident macrophage populations. Despite expression of relevant activating FcγRs on various phagocyte populations, our data indicate that the majority of these cell types are dispensable for IgG activity in vivo. In contrast, IgG-dependent effector functions were selectively impaired in animals lacking the CX CR1 Ly6C CD11c monocyte subset, which expressed the full set of FcγRs required for IgG activity. © 2011 Elsevier Inc.
APA:
Biburger, M., Aschermann, S., Schwab, I., Lux, A., Albert, H., Danzer, H.,... Nimmerjahn, F. (2011). Monocyte Subsets Responsible for Immunoglobulin G-Dependent Effector Functions In Vivo. Immunity, 35(6), 932-944. https://doi.org/10.1016/j.immuni.2011.11.009
MLA:
Biburger, Markus, et al. "Monocyte Subsets Responsible for Immunoglobulin G-Dependent Effector Functions In Vivo." Immunity 35.6 (2011): 932-944.
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