Antibody (Ab)-mediated bacterial opsonization is essential for protective immunity against Streptococcus pneumoniae in humans, as attested to by the frequent occurrence of invasive pneumococcal disease (IPD) in patients with B cell primary immunodeficiencies (PIDs) and impaired Ab response to pneumococcal capsular glycansi'2. Carrying forward the theme of B cell immunity in this Program Project, we aim to decipher new molecular genetic bases of three otherwise distinct PIDs sharing both impaired Ab response to glycans and predisposition to IPD, (i) anhidrotic ectodermal dysplasia vdth immunodeficiency (EDA-ID), (ii) specific antibody deficiency (SPAD) and IgGa deficiency (IgG2D), and (iii) common variable immunodeficiency (CVID). EDA-ID is a rare syndromic PID of childhood, associated with recurrent IPD and abolished Ab response to glycans3'4, due in most cases to mutations in NEMO and IKBQ, which underlie, respectively, X- linked recessive (XR) and autosomal dominant (AD) formsS'^. SPAD and IgG2D confer a more selective impairment of Ab response to glycans, which may lead to IPD^'S, and are rarely caused by mutations in the IgG2 locus itself, with autosomal recessive (AR) inheritance^''^. CVID is more common, associated with a global decrease in IgG levels, impaired Ab response to glycans and IPD in adults'3, and rarely caused by AR mutations in ICOS, TACI, BAFF-R, CD19, CD20 and CDSi's-ie. We hypothesize that genetically unexplained EDA-ID, SPAD/IgG2D, or CVID result from novel inborn errors. We thus aim to decipher novel IPD- predisposing single-gene inborn errors of Ab-mediated immunity to glycans in patients with these PIDs. We will use genome-wide approaches, taking advantage of the recent advent of whole-exome and -genome sequencing, which have been pioneered in the lab for human PIDs'^.is. The immunological consequences of the mutant alleles v all be studied in collaboration with other teams of this project. Our preliminary data are exciting, as we recently identified new genetic etiologies of EDA-ID (mutations in P2Y4) and SPAD/IgG2D (mutations in RBCKi and TIFA). We also obtained our first whole-exome data for young subjects with CVTD. This project will result in the discovery of new genetic etiologies of three distinct PIDs sharing impaired Ab responses to glycans and predisposition to IPD. The immunological implications of this study are important, as it will shed a new light onto the genetic control of human Ab responses to glycans and protective immunity to pneumococcus. The clinical implications are equally critical, as our results will provide families with genetic counseling and pave the way for investigation of the genetic basis of IPD and B cell PIDs in other patients.

Public Health Relevance

Impaired antibody (Ab) response to pneumococcus often results in invasive pneumococcal disease (IPD), sue! as septicemia or meningitis. In most patients wdth IPD and impaired Ab response to pneumococcus, the illnes; is thought to be genetically determined, but there is no known genetic underlying anomaly. We intend tc decipher the molecular genetic basis of three conditions associated wdth impaired Ab to pneumococcus anc IPD.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI061093-09
Application #
8381511
Study Section
Special Emphasis Panel (ZAI1-PA-I)
Project Start
Project End
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
9
Fiscal Year
2012
Total Cost
$541,613
Indirect Cost
$127,563
Name
Icahn School of Medicine at Mount Sinai
Department
Type
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Casanova, Jean-Laurent; Abel, Laurent (2017) Human genetics of infectious diseases: Unique insights into immunological redundancy. Semin Immunol :
Boisson, Bertrand; Puel, Anne; Picard, Capucine et al. (2017) Human I?B? Gain of Function: a Severe and Syndromic Immunodeficiency. J Clin Immunol 37:397-412
Gernez, Yael; Freeman, Alexandra F; Holland, Steven M et al. (2017) Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry. J Allergy Clin Immunol Pract :
Schickel, Jean-Nicolas; Glauzy, Salomé; Ng, Yen-Shing et al. (2017) Self-reactive VH4-34-expressing IgG B cells recognize commensal bacteria. J Exp Med 214:1991-2003
Perkins, Tiffany; Rosenberg, Jacob M; Le Coz, Carole et al. (2017) Smith-Magenis Syndrome Patients Often Display Antibody Deficiency but Not Other Immune Pathologies. J Allergy Clin Immunol Pract 5:1344-1350.e3
Ma, Chi A; Stinson, Jeffrey R; Zhang, Yuan et al. (2017) Germline hypomorphic CARD11 mutations in severe atopic disease. Nat Genet 49:1192-1201
Magri, Giuliana; Comerma, Laura; Pybus, Marc et al. (2017) Human Secretory IgM Emerges from Plasma Cells Clonally Related to Gut Memory B Cells and Targets Highly Diverse Commensals. Immunity 47:118-134.e8
Albin-Leeds, Stephanie; Ochoa, Juliana; Mehta, Harshna et al. (2017) Idiopathic T cell lymphopenia identified in New York State Newborn Screening. Clin Immunol 183:36-40
Di Niro, R; Snir, O; Kaukinen, K et al. (2016) Responsive population dynamics and wide seeding into the duodenal lamina propria of transglutaminase-2-specific plasma cells in celiac disease. Mucosal Immunol 9:254-64
Scott, Eric M; Halees, Anason; Itan, Yuval et al. (2016) Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nat Genet 48:1071-6

Showing the most recent 10 out of 153 publications