Killer cell immunoglobulin-like receptor and human leukocyte antigen gene profiles in a cohort of HIV-infected Mexican Mestizos.

Abstract:

:Killer cell immunoglobulin-like receptors (KIRs) represent the most polymorphic genes responsible for natural killer cell function, while human leukocyte antigen (HLA) class I molecules define and restrict cytotoxic T lymphocyte responses. Specific KIR, HLA, or KIR-HLA combinations have been implicated in the outcome of human immunodeficiency virus (HIV) disease. The remarkable polymorphism of KIR and HLA genes warrants descriptive gene frequency studies in different populations, as well as their impact on HIV disease progression in different immunogenetic contexts. We report KIR and HLA class I gene profiles of 511 unrelated HIV-infected Mexican Mestizo individuals from 18 states for whom genetic ancestry proportions were assessed. KIR and HLA gene profiles were compared between individuals from the north and central-south regions of the country and between individuals with higher European (EUR) or Amerindian (AMI) genetic ancestry component. A total of 65 KIR genotypes were observed, 11 harboring novel KIR gene combinations. A total of 164 HLA alleles were observed: 43 HLA-A, 87 HLA-B, and 34 HLA-C. Differences in the distribution of 12 HLA alleles were observed between individuals with higher AMI or EUR ancestry components (p < 0.05, q < 0.2). After correcting for genetic ancestry, only individual HLA alleles were associated with HIV disease progression, including a novel association with A*02:06, an Amerindian HLA allele associated with lower CD4+ T cell counts. No KIR effects were significant. Our results highlight the advantages of considering a detailed genetic stratification within populations when studying genetic profiles that could be implicated in disease-association studies.

journal_name

Immunogenetics

journal_title

Immunogenetics

authors

Garrido-Rodríguez D,Ávila-Ríos S,García-Morales C,Valenzuela-Ponce H,Ormsby C,Reyes-Gopar H,Fernandez-Lopez JC,Reyes-Terán G

doi

10.1007/s00251-016-0920-3

subject

Has Abstract

pub_date

2016-10-01 00:00:00

pages

703-17

issue

9

eissn

0093-7711

issn

1432-1211

pii

10.1007/s00251-016-0920-3

journal_volume

68

pub_type

杂志文章
  • Sequence polymorphism in the HLA-B promoter region.

    abstract::Transcription of major histocompatibility complex class I genes is controlled by the class I regulatory complex in the 5' flanking region. To investigate the molecular basis of this region, we studied the polymorphism of the promoter of the HLA-B locus extending from the ATG transcription initiation signal to -284 bas...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00163991

    authors: Yao Z,Volgger A,Scholz S,Albert ED

    更新日期:1995-01-01 00:00:00

  • Large-scale identification and characterization of genetic variants in asthma candidate genes.

    abstract::Asthma is a chronic inflammatory disorder of the airways, and a number of genetic loci are associated with the disease. Candidate gene association studies have been regarded as effective tools to study complex traits. Knowledge of the sequence variation and structure of the candidate genes is required for association ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-005-0024-y

    authors: Kim JJ,Kim HH,Park JH,Ryu HJ,Kim J,Moon S,Gu H,Kim HT,Lee JY,Han BG,Park C,Kimm K,Park CS,Lee JK,Oh B

    更新日期:2005-10-01 00:00:00

  • Characterization of horse (Equus caballus) T-cell receptor beta chain genes.

    abstract::Genes encoding the horse (Equus caballus) T-cell receptor beta chain (TCRB) were cloned and characterized. Of 33 cDNA clones isolated from the mesenteric lymph node, 30 had functionally rearranged gene segments, and three contained germline sequences. Sixteen unique variable segments (TCRBV), 14 joining genes (TCRBJ),...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00188177

    authors: Schrenzel MD,Watson JL,Ferrick DA

    更新日期:1994-01-01 00:00:00

  • cDNA cloning and localization of the mouse leukosialin gene (Ly48) to chromosome 7.

    abstract::Mouse leukosialin, previously known as the 3E8 antigen, is expressed primarily on cells of the hematopoietic and lymphoid lineages and is shown to be the mouse homologue to the human leukosialin/sialophorin and rat W3/13 molecules. A partial leukosialin cDNA clone was isolated via cross-species hybridization with a po...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF02115004

    authors: Baecher CM,Dorfman KS,Mattei MG,Frelinger JG

    更新日期:1990-01-01 00:00:00

  • MICA-A5.1 allele is associated with atypical forms of celiac disease in HLA-DQ2-negative patients.

    abstract::We selected 38 consecutive celiac disease (CD) patients (from a group of 316 consecutive CD patients) and 91 healthy blood donors, all of whom were HLA-DQ2 (DQA1*0501/DQB1*0201) negative, and investigated the presence of the classically associated alleles HLA-DQ8 and HLA-DRB4. We also studied the distribution of MICA ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-001-0413-9

    authors: Lopez-Vazquez A,Rodrigo L,Fuentes D,Riestra S,Bousoño C,Garcia-Fernandez S,Martinez-Borra J,Gonzalez S,Lopez-Larrea C

    更新日期:2002-02-01 00:00:00

  • Polymorphisms in recent GWA identified asthma genes CA10, SGK493, and CTNNA3 are associated with disease severity and treatment response in childhood asthma.

    abstract::Recent genome-wide association studies (GWAs) have identified several new genetic risk factors for asthma; however, their influence on disease behavior and treatment response is still unclear. The aim of our study was the association analysis of the most significant single nucleotide polymorphisms (SNPs) recently repo...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-013-0755-0

    authors: Perin P,Potočnik U

    更新日期:2014-03-01 00:00:00

  • The role of upstream stimulatory factor 1 in the transcriptional regulation of the human TBX21 promoter mediated by the T-1514C polymorphism associated with systemic lupus erythematosus.

    abstract::T-bet is a key regulator for the lineage commitment in CD4+ T helper (Th) 1 cells by activating the hallmark production of interferon-γ. Previously, two single nucleotide polymorphisms (SNPs) in the TBX21 promoter, T-1993C and T-1514C, have been shown by statistic studies to associate with systemic lupus erythematosus...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-011-0597-6

    authors: Li J,Li J,You Y,Chen S

    更新日期:2012-05-01 00:00:00

  • Copy number and nucleotide variation of the LILR family of myelomonocytic cell activating and inhibitory receptors.

    abstract::Leukocyte immunoglobulin-like receptors (LILR) are cell surface molecules that regulate the activities of myelomonocytic cells through the balance of inhibitory and activation signals. LILR genes are located within the leukocyte receptor complex (LRC) on chromosome 19q13.4 adjacent to KIR genes, which are subject to a...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-013-0742-5

    authors: López-Álvarez MR,Jones DC,Jiang W,Traherne JA,Trowsdale J

    更新日期:2014-02-01 00:00:00

  • Haplotypic variation of the transporter associated with antigen processing (TAP) genes and their extension of HLA class II region haplotypes.

    abstract::Stable cell surface presentation of HLA class I molecules requires active transport of antigenic peptides across the endoplasmic reticulum by products of two genes, TAP1 and TAP2, which map in the major histocompatibility complex class II region. Alleles of each gene are derived from a combination of variable sites at...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00187452

    authors: Carrington M,Colonna M,Spies T,Stephens JC,Mann DL

    更新日期:1993-01-01 00:00:00

  • Large-scale analysis of HLA peptides presented by HLA-Cw4.

    abstract::A large number of HLA-Cw4 (Cw *0402) peptides were purified, sequenced, and identified from breast and ovarian carcinoma cell lines. HLA-Cw4 molecules were expressed in these cells as soluble, secreted HLA (sHLA) and recovered from the growth medium. The peptides were separated by capillary reversed-phase HPLC and ana...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-003-0570-0

    authors: Buchsbaum S,Barnea E,Dassau L,Beer I,Milner E,Admon A

    更新日期:2003-06-01 00:00:00

  • MHC class II polymorphism is associated with a canine SLE-related disease complex.

    abstract::Nova Scotia duck tolling retrievers are predisposed to a SLE-related disease complex including immune-mediated rheumatic disease (IMRD) and steroid-responsive meningitis-arteritis (SRMA). IMRD involves symptoms that resemble those seen in systemic autoimmune rheumatic diseases, such as systemic lupus erythematosus, SL...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-009-0387-6

    authors: Wilbe M,Jokinen P,Hermanrud C,Kennedy LJ,Strandberg E,Hansson-Hamlin H,Lohi H,Andersson G

    更新日期:2009-08-01 00:00:00

  • cDNA cloning of human DEC-205, a putative antigen-uptake receptor on dendritic cells.

    abstract::Dendritic cells (DC) are specialist antigen presenting cells which capture antigens in the periphery, migrate centrally, and present the processed antigens in the context of major histocompatibility complex and appropriate co-stimulatory molecules to T lymphocytes for the initiation of an immune response. DEC-205 has ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510050381

    authors: Kato M,Neil TK,Clark GJ,Morris CM,Sorg RV,Hart DN

    更新日期:1998-05-01 00:00:00

  • A biochemical characterization of feline MHC products: unusually high expression of class II antigens on peripheral blood lymphocytes.

    abstract::The polymorphism of feline MHC antigens was examined using biochemical methods. The following observations were made: (1) feline class I and II antigens are polymorphic. Their biochemical features were established using rabbit and mouse reagents directed against human MHC products; they resemble those observed for oth...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00398799

    authors: Neefjes JJ,Hensen EJ,de Kroon TI,Ploegh HL

    更新日期:1986-01-01 00:00:00

  • Altered structure of HLA class I heavy chains associated with mouse beta-2 microglobulin.

    abstract::The serological reactivities of HLA-A3, -B7, and -CW3 heavy chains associated with either mouse, bovine, or human beta-2-microglobulin (beta 2m) and expressed on the surface of transfected mouse fibroblasts were analyzed. All reactivities associated with one cluster (defined by monoclonal antibody W6/32) of antigenic ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00430798

    authors: Ferrier P,Fontecilla-Camps JC,Bucchini D,Caillol DH,Jordan BR,Lemonnier FA

    更新日期:1985-01-01 00:00:00

  • Comparative analysis of nonaspanin protein sequences and expression studies in zebrafish.

    abstract::Nonaspanins constitute a family of proteins, also called TM9SF, characterized by a large non-cytoplasmic domain and nine putative transmembrane domains. This family is highly conserved through evolution and comprises three members in Saccharomyces cerevisiae, Dictyostelium discoideum, and Drosophila melanogaster, and ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-010-0472-x

    authors: Pruvot B,Laurens V,Salvadori F,Solary E,Pichon L,Chluba J

    更新日期:2010-10-01 00:00:00

  • The dichotomous size variation of human complement C4 genes is mediated by a novel family of endogenous retroviruses, which also establishes species-specific genomic patterns among Old World primates.

    abstract::The human complement C4 genes in the HLA exhibit an unusual, dichotomous size polymorphism and a four-gene, modular variation involving novel gene RP, complement C4, steroid 21-hydroxylase (CYP21), and tenascin-like Gene X (RCCX). The C4 gene size dichotomy is mediated by an endogenous retrovirus, HERV-K(C4). Nearly i...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00177825

    authors: Dangel AW,Mendoza AR,Baker BJ,Daniel CM,Carroll MC,Wu LC,Yu CY

    更新日期:1994-01-01 00:00:00

  • Differential expression of two Carassius auratus Mx genes in cultured CAB cells induced by grass carp hemorrhage virus and interferon.

    abstract::UV-inactivated GCHV (grass carp hemorrhage virus) is able to induce an antiviral state in cultured CAB cells (crucian carp Carassius auratus blastulae embryonic cells) via the production of interferon (IFN). In the current work, the full-length cDNAs of two Mx genes, termed CaMx1 and CaMx2, have been cloned and sequen...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-004-0658-1

    authors: Zhang YB,Li Q,Gui JF

    更新日期:2004-04-01 00:00:00

  • H-2 influences phenytoin binding and inhibition of prostaglandin synthesis.

    abstract::We have reported that susceptibility to glucocorticoid- and phenytoin-induced cleft palate and glucocorticoid receptor levels in mice are influenced by the H-2 histocompatibility complex on chromosome 17. Phenytoin competes with glucocorticoids for the glucocorticoid receptor and inhibits production of prostaglandins ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00430325

    authors: Gupta C,Katsumata M,Goldman AS

    更新日期:1984-01-01 00:00:00

  • Coordinate loss of MHC class II expression in the diffuse large B cell lymphoma cell line OCI-Ly2 is due to a novel mutation in RFX-AP.

    abstract::Loss of major histocompatibility complex class II (MHCII) antigen expression on diffuse large B cell lymphoma (DLBCL) corresponds closely with significant decreases in patient survival. However, the mechanisms accounting for MHCII loss in DLBCL have not been thoroughly characterized to date. In this report, we demonst...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-009-0418-3

    authors: Bushway M,Cycon KA,Mulvaney K,Murphy SP

    更新日期:2010-02-01 00:00:00

  • Lyb-8.2: A new B cell antigen defined and characterized with a monoclonal antibody.

    abstract::A DBA/1 B10.D2-specific monoclonal antibody (CY34) is described which defines a new murine B lymphocyte differentiation antigen designated Lyb-8.2. The ontogeny, strain distribution, and cell-surface density of the antigen were studied by radioimmunoassay and by fluorescence-activated cell sorter (FACS) analysis. Lyb-...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00372098

    authors: Symington FW,Subbarao B,Mosier DE,Sprent J

    更新日期:1982-01-01 00:00:00

  • Mhc haplotype H6 is associated with sustained control of SIVmac251 infection in Mauritian cynomolgus macaques.

    abstract::The restricted diversity of the major histocompatibility complex (MHC) of Mauritian cynomolgus macaques provides powerful opportunities for insight into host-viral interactions and cellular immune responses that restrict lentiviral infections. However, little is known about the effects of Mhc haplotypes on control of ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-009-0369-8

    authors: Mee ET,Berry N,Ham C,Sauermann U,Maggiorella MT,Martinon F,Verschoor EJ,Heeney JL,Le Grand R,Titti F,Almond N,Rose NJ

    更新日期:2009-05-01 00:00:00

  • Characteristics of initial and reinduced experimental autoimmune encephalomyelitis.

    abstract::The factors which influence expression of autoimmune disease in the central nervous system are still poorly understood. We determined the characteristics of experimental autoimmune encephalomyelitis (EAE) in twelve different inbred strains of mice using either mouse spinal cord homogenate or synthetic peptides as the ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF02602559

    authors: Lindsey JW

    更新日期:1996-01-01 00:00:00

  • Position 45 influences the peptide binding motif of HLA-B*44:08.

    abstract::Position 45 represents a highly polymorphic residue within HLA class I alleles, which contacts the p2 position of bound peptides in 85% of the peptide-HLA structures analyzed, while the neighboring residues 41 and 46 are not involved in peptide binding. To investigate the influence of residue 45 at the functional leve...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-011-0583-z

    authors: Badrinath S,Huyton T,Schumacher H,Blasczyk R,Bade-Doeding C

    更新日期:2012-03-01 00:00:00

  • A mutation in KIR3DS1 that results in truncation and lack of cell surface expression.

    abstract::The KIR gene cluster exhibits a high degree of polymorphism in terms of gene content as well as allelic polymorphism, and data suggest that it is evolving rapidly. The KIR3DL1 locus is one of the most polymorphic loci within this cluster and is unique in that it encodes an activating receptor KIR3DS1, as well as multi...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-007-0240-8

    authors: Martin MP,Pascal V,Yeager M,Phair J,Kirk GD,Hoots K,O'Brien SJ,Anderson SK,Carrington M

    更新日期:2007-10-01 00:00:00

  • Evolutionary history of the Rh blood group-related genes in vertebrates.

    abstract::Rh and its homologous Rh50 gene products are considered to form heterotetramers on erythrocyte membranes. Rh protein has Rh blood group antigen sites, while Rh50 protein does not, and is more conserved than Rh protein. We previously determined both Rh and Rh50 gene cDNA coding regions from mouse and rat, and carried o...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510000202

    authors: Kitano T,Saitou N

    更新日期:2000-08-01 00:00:00

  • Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS.

    abstract::Apoptosis has been suggested as a major mechanism for the CD4(+) T-lymphocyte depletion observed in patients infected with human immunodeficiency virus 1 (HIV-1). To evaluate the impact of genetic variations to apoptosis during progression of acquired immunodeficiency syndrome (AIDS), we have performed an extensive ge...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-004-0664-3

    authors: Vasilescu A,Heath SC,Diop G,Do H,Hirtzig T,Hendel H,Bertin-Maghit S,Rappaport J,Therwath A,Lathrop GM,Matsuda F,Zagury JF

    更新日期:2004-04-01 00:00:00

  • The gene encoding the Ia-associated invariant chain is located on chromosome 18 in the mouse.

    abstract::The chromosomal assignment of the gene encoding the invariant (Ii) chain associated with the mouse immune response antigens (Ia) was determined by Southern blot analysis of DNA from a panel of mouse X Chinese hamster somatic cell hybrids cleaved with Hind III or Eco RI. Using a mouse li cDNA as a hybridization probe, ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00372244

    authors: Yamamoto K,Floyd-Smith G,Francke U,Koch N,Lauer W,Dobberstein B,Schäfer R,Hämmerling GJ

    更新日期:1985-01-01 00:00:00

  • Structural and functional characterisation of the Toll like receptor 9 of Aotus nancymaae, a non-human primate model for malaria vaccine development.

    abstract::In the absence of suitable rodent animal models for Plasmodium falciparum malaria, the efficacy testing of asexual blood-stage vaccine candidates in Aotus nancymaae represents a tool to select between different formulations before conducting expensive human clinical trials. CpG oligonucleotides (ODN) specifically prom...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-005-0789-z

    authors: Spirig R,Peduzzi E,Patarroyo ME,Pluschke G,Daubenberger CA

    更新日期:2005-05-01 00:00:00

  • Diversity of the human LILRB3/A6 locus encoding a myeloid inhibitory and activating receptor pair.

    abstract::Leukocyte immunoglobulin-like receptor (LILR)B3 and LILRA6 represent a pair of inhibitory/activating receptors with identical extracellular domains and unknown ligands. LILRB3 can mediate inhibitory signaling via immunoreceptor tyrosine-based inhibition motifs in its cytoplasmic tail whereas LILRA6 can signal through ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-013-0730-9

    authors: Bashirova AA,Apps R,Vince N,Mochalova Y,Yu XG,Carrington M

    更新日期:2014-01-01 00:00:00

  • Polymorphisms in the human surfactant protein-D (SFTPD) gene: strong evidence that serum levels of surfactant protein-D (SP-D) are genetically influenced.

    abstract::The collectin surfactant protein-D (SP-D) plays a significant role in innate immunity. Epidemiological studies described associations between single nucleotide polymorphisms (SNPs) of the human gene coding surfactant protein-D (SFTPD) and infectious pulmonary diseases. Studies on twins indicated very strong genetic de...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-005-0775-5

    authors: Heidinger K,König IR,Bohnert A,Kleinsteiber A,Hilgendorff A,Gortner L,Ziegler A,Chakraborty T,Bein G

    更新日期:2005-04-01 00:00:00