Adaptive Immune Response to Model Antigens Is Impaired in Murine Leukocyte-Adhesion Deficiency-1 Revealing Elevated Activation Thresholds In Vivo. (4th March 2012)

• Record Type: Journal Article
• Authors: Peters, Thorsten; Bloch, Wilhelm; Pabst, Oliver; Wickenhauser, Claudia; Uthoff-Hachenberg, Claudia; Schmidt, Susanne V.; Varga, Georg; Grabbe, Stephan; Kess, Daniel; Oreshkova, Tsvetelina; Sindrilaru, Anca; Addicks, Klaus; Förster, Reinhold; Müller, Werner; Scharffetter-Kochanek, Karin
• Other Names: Basso Alexandre S. Academic Editor.
• Is Part Of: Clinical & developmental immunology. Volume 2012(2012)
• Publication Date: 2012-03-04
• Subjects: Developmental immunology -- Periodicals; Clinical immunology -- Periodicals; Immune System -- immunology -- Periodicals; Immune System -- growth & development -- Periodicals; Immune System Diseases -- immunology -- Periodicals; 571.9638
• DOI: 10.1155/2012/450738
• Languages: English
• ISSNs: 1740-2522

Abstract

Abstract : Absence of β 2 integrins (CD11/CD18) leads to leukocyte-adhesion deficiency-1 (LAD1), a rare primary immunodeficiency syndrome. Although extensive in vitro work has established an essential function of β 2 integrins in adhesive and signaling properties for cells of the innate and adaptive immune system, their respective participation in an altered adaptive immunity in LAD1 patients are complex and only partly understood in vivo . Therefore, we investigated adaptive immune responses towards different T-dependent antigens in a murine LAD1 model of β 2 integrin-deficiency (CD18 −/− ). CD18 −/− mice generated only weak IgG responses after immunization with tetanus toxoid (TT). In contrast, robust hapten- and protein-specific immune responses were observed after immunization with highly haptenated antigens such as (4-hydroxy-3-nitrophenyl)21 acetyl chicken γ globulin (NP21 -CG), even though regularly structured germinal centers with specificity for the defined antigens/haptens in CD18 −/− mice remained absent. However, a decrease in the hapten/protein ratio lowered the efficacy of immune responses in CD18 −/− mice, whereas a mere reduction of the antigen dose was less crucial. Importantly, haptenation of TT with NP (NP-TT) efficiently restored a robust IgG response also to TT. Our findings may stimulate further studies on a modification of vaccination strategies using highly haptenated antigens in individuals suffering from LAD1.