Germline deletion of CIN85 in humans with X chromosome–linked antibody deficiency

Author:

Keller Baerbel1ORCID,Shoukier Moneef2ORCID,Schulz Kathrin3,Bhatt Arshiya3,Heine Ines3,Strohmeier Valentina1,Speckmann Carsten2,Engels Niklas3ORCID,Warnatz Klaus1,Wienands Jürgen3ORCID

Affiliation:

1. Center for Chronic Immunodeficiency, Medical Center–University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany

2. Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany

3. Institute of Cellular & Molecular Immunology, University Medical Center Göttingen, Göttingen, Germany

Abstract

Ubiquitously expressed Cbl-interacting protein of 85 kD (CIN85) is a multifunctional adapter molecule supposed to regulate numerous cellular processes that are critical for housekeeping as well as cell type–specific functions. However, limited information exists about the in vivo roles of CIN85, because only conditional mouse mutants with cell type–specific ablation of distinct CIN85 isoforms in brain and B lymphocytes have been generated so far. No information is available about the roles of CIN85 in humans. Here, we report on primary antibody deficiency in patients harboring a germline deletion within the CIN85 gene on the X chromosome. In the absence of CIN85, all immune cell compartments developed normally, but B lymphocytes showed intrinsic defects in distinct effector pathways of the B cell antigen receptor, most notably NF-κB activation and up-regulation of CD86 expression on the cell surface. These results reveal nonredundant functions of CIN85 for humoral immune responses.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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