Human CD1a Deficiency Is Common and Genetically Regulated

CD1 proteins evolved to present diverse lipid Ags to T cells. In comparison with MHC proteins, CD1 proteins exhibit minimal allelic diversity as a result of nonsynonymous single nucleotide polymorphisms (SNPs). However, it is unknown if common SNPs in gene regulatory regions affect CD1 expression and function. We report surprising diversity in patterns of inducible CD1a expression on human dendritic cells (DCs), spanning the full range from undetectable to high density, a finding not seen with other CD1 isoforms. CD1a-deficient DCs failed to present mycobacterial lipopeptide to T cells but had no defects in endocytosis, cytokine secretion, or expression of costimulatory molecules after LPS treatment. We identified an SNP in the 5′ untranslated region (rs366316) that was common and strongly associated with low CD1a surface expression and mRNA levels (p = 0.03 and p = 0.001, respectively). Using a CD1a promoter-luciferase system in combination with mutagenesis studies, we found that the polymorphic allele reduced luciferase expression by 44% compared with the wild-type variant (p < 0.001). Genetic regulation of lipid Ag presentation by varying expression on human DCs provides a mechanism for achieving population level differences in immune responses despite limited structural variation in CD1a proteins.

[1]  M. McElrath,et al.  Enumeration of major peripheral blood leukocyte populations for multicenter clinical trials using a whole blood phenotyping assay. , 2012, Journal of visualized experiments : JoVE.

[2]  L. Reynard,et al.  Expression of the osteoarthritis-associated gene GDF5 is modulated epigenetically by DNA methylation. , 2011, Human molecular genetics.

[3]  M. Pace,et al.  Polymorphism of CD1 and SH2D2A genes in inflammatory neuropathies , 2011, Journal of the peripheral nervous system : JPNS.

[4]  A. Scelfo,et al.  High‐frequency and adaptive‐like dynamics of human CD1 self‐reactive T cells , 2011, European journal of immunology.

[5]  R. Clark,et al.  CD1a-autoreactive T cells are a normal component of the human αβ T cell repertoire , 2010, Nature Immunology.

[6]  G. De Libero,et al.  Early Recycling Compartment Trafficking of CD1a Is Essential for Its Intersection and Presentation of Lipid Antigens , 2009, The Journal of Immunology.

[7]  M. Pelizzo,et al.  The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/USF2 Transcription Factors , 2009, PLoS genetics.

[8]  I. van Rhijn,et al.  The evolved functions of CD1 during infection. , 2009, Current opinion in immunology.

[9]  D. Zajonc,et al.  Synthesis of Dideoxymycobactin Antigens Presented by CD1a Reveals T Cell Fine Specificity for Natural Lipopeptide Structures* , 2009, The Journal of Biological Chemistry.

[10]  G. Watts,et al.  CD1a expression defines an interleukin‐12 producing population of human dendritic cells , 2009, Clinical and experimental immunology.

[11]  James Robinson,et al.  The IMGT/HLA database , 2008, Nucleic Acids Res..

[12]  D. Moody,et al.  IgG regulates the CD1 expression profile and lipid antigen-presenting function in human dendritic cells via FcgammaRIIa. , 2008, Blood.

[13]  F. Morel,et al.  A role for T cell‐derived interleukin 22 in psoriatic skin inflammation , 2007, Clinical and experimental immunology.

[14]  L. Nagy,et al.  Differentiation of CD1a- and CD1a+ monocyte-derived dendritic cells is biased by lipid environment and PPARgamma. , 2007, Blood.

[15]  S. Peng,et al.  Mycobacterium tuberculosis Regulates CD1 Antigen Presentation Pathways through TLR-21 , 2005, The Journal of Immunology.

[16]  I. Wilson,et al.  T cell activation by lipopeptide antigens. , 2005, Science.

[17]  Michael B Brenner,et al.  CD1: antigen presentation and T cell function. , 2004, Annual review of immunology.

[18]  Sebastian Böcker,et al.  High-throughput MALDI-TOF discovery of genomic sequence polymorphisms. , 2003, Genome research.

[19]  I. Wilson,et al.  Crystal structure of CD1a in complex with a sulfatide self antigen at a resolution of 2.15 Å , 2003, Nature Immunology.

[20]  D. Labie,et al.  Two novel CD1 E alleles identified in black African individuals. , 2002, Tissue antigens.

[21]  G. De Libero,et al.  Presentation of the Same Glycolipid by Different CD1 Molecules , 2002, The Journal of experimental medicine.

[22]  F. Setién,et al.  Structural characterization of two CD1A allelic variants. , 2001, Human immunology.

[23]  J. Punnonen,et al.  Monocyte-Derived CD1a+ and CD1a− Dendritic Cell Subsets Differ in Their Cytokine Production Profiles, Susceptibilities to Transfection, and Capacities to Direct Th Cell Differentiation1 , 2000, The Journal of Immunology.

[24]  E. Martínez-Naves,et al.  Identification of two novel human CD1E alleles. , 2000, Tissue antigens.

[25]  E. V. van Donselaar,et al.  Separate pathways for antigen presentation by CD1 molecules. , 1999, Immunity.

[26]  L. Hannick,et al.  Polymorphism of human CD1 genes. , 1999, Tissue antigens.

[27]  T. Ito,et al.  A CD1a+/CD11c+ subset of human blood dendritic cells is a direct precursor of Langerhans cells. , 1999, Journal of immunology.

[28]  F. Setién,et al.  Single strand conformational polymorphism analysis of human CD1 genes in different ethnic groups. , 1999, Tissue antigens.

[29]  E. Grant,et al.  CD1-Restricted Microbial Lipid Antigen-Specific Recognition Found in the CD8+ αβ T Cell Pool , 1999, The Journal of Immunology.

[30]  S. Ichimiya,et al.  Structural analysis of the rat homologue of CD1. Evidence for evolutionary conservation of the CD1D class and widespread transcription by rat cells. , 1994, Journal of immunology.

[31]  F. Sallusto,et al.  Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha , 1994, The Journal of experimental medicine.

[32]  C. Thompson,et al.  Characterization of dermal dendritic cells obtained from normal human skin reveals phenotypic and functionally distinctive subsets. , 1993, Journal of immunology.

[33]  S. Porcelli,et al.  CDlb restricts the response of human CD4−8−T lymphocytes to a microbial antigen , 1992, Nature.

[34]  S. Balk,et al.  Isolation and expression of cDNA encoding the murine homologues of CD1. , 1991, Journal of immunology.

[35]  S. Balk,et al.  Recognition of cluster of differentiation 1 antigens by human CD4−CD8>− cytolytic T lymphocyte , 1989, Nature.

[36]  C. Milstein,et al.  Mouse CD1 is distinct from and co‐exists with TL in the same thymus. , 1988, The EMBO journal.

[37]  C. Milstein,et al.  Structure and expression of the human thymocyte antigens CD1a, CD1b, and CD1c. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[38]  C. Milstein,et al.  Isolation of CD1 genes: a family of major histocompatibility complex-related differentiation antigens. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[39]  C. Dascher Evolutionary biology of CD1. , 2007, Current topics in microbiology and immunology.

[40]  D. van den Boom,et al.  MALDI-TOF mass spectrometry-based SNP genotyping. , 2003, Methods in molecular biology.

[41]  E. Grant,et al.  CD1-restricted microbial lipid antigen-specific recognition found in the CD8+ alpha beta T cell pool. , 1999, Journal of immunology.