Time to Seroconversion in HIV-Exposed Subjects Carrying Protective versus Non Protective KIR3DS1/L1 and HLA-B Genotypes
Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface killer immunoglobulin-like receptor locus KIR3DL1/S1 have been shown to influence time to AIDS in HIV-infected individuals and risk of seroconver...
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Published in | PloS one Vol. 9; no. 10; p. e110480 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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17.10.2014
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Abstract | Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface killer immunoglobulin-like receptor locus KIR3DL1/S1 have been shown to influence time to AIDS in HIV-infected individuals and risk of seroconversion in HIV exposed seronegative (HESN) subjects. Here, we assessed time to seroconversion or duration of seronegative status in a group of 168 HIV exposed individuals, including 74 seroconverters and 94 HESN based on carriage or not of KIR3DL1/S1/HLA-B genotypes previously shown to be associated with protection from infection and/or slow time to AIDS. KIR3DL1/S1 genotyping was performed by sequence-specific primer polymerase chain reaction using two pairs of specific primers for each locus. The MHC class IB locus was typed to four-position resolution to resolve Bw4 and Bw6 alleles and the amino acid present at position 80. KIR3DL1/S1 heterozygotes became HIV infected significantly faster than KIR3DS1 homozygotes. Individuals who carried both KIR3DS1 and Bw4*80I did not remain HIV seronegative longer than those from a control group who were homozygous for HLA-Bw6 and carried no HLA-A locus Bw4 alleles Subjects who were *h/*y+B*57 showed a trend towards slower time to serconversion than those with other KIR3DL1 homozygous and KIR3DL1/S1 heterozygous genotypes. Thus, KIR3DS1 homozygosity is associated with protection from HIV infection while co-carriage of KIR3DS1 and Bw4*80I is not. The requirements for protection from HIV infection can differ from those that influence time to AIDS in HIV infected individuals. |
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AbstractList | Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic
HLA-B
locus and the NK cell surface killer immunoglobulin-like receptor locus
KIR3DL1/S1
have been shown to influence time to AIDS in HIV-infected individuals and risk of seroconversion in HIV exposed seronegative (HESN) subjects. Here, we assessed time to seroconversion or duration of seronegative status in a group of 168 HIV exposed individuals, including 74 seroconverters and 94 HESN based on carriage or not of
KIR3DL1/S1/HLA-B
genotypes previously shown to be associated with protection from infection and/or slow time to AIDS.
KIR3DL1/S1
genotyping was performed by sequence-specific primer polymerase chain reaction using two pairs of specific primers for each locus. The MHC class IB locus was typed to four-position resolution to resolve
Bw4
and
Bw6
alleles and the amino acid present at position 80.
KIR3DL1/S1
heterozygotes became HIV infected significantly faster than
KIR3DS1
homozygotes. Individuals who carried both
KIR3DS1
and
Bw4*80I
did not remain HIV seronegative longer than those from a control group who were homozygous for
HLA-Bw6
and carried no
HLA-A
locus
Bw4
alleles Subjects who were
*h/*y+B*57
showed a trend towards slower time to serconversion than those with other
KIR3DL1
homozygous and
KIR3DL1/S1
heterozygous genotypes. Thus,
KIR3DS1
homozygosity is associated with protection from HIV infection while co-carriage of
KIR3DS1
and
Bw4*80I
is not. The requirements for protection from HIV infection can differ from those that influence time to AIDS in HIV infected individuals. Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface killer immunoglobulin-like receptor locus KIR3DL1/S1 have been shown to influence time to AIDS in HIV-infected individuals and risk of seroconversion in HIV exposed seronegative (HESN) subjects. Here, we assessed time to seroconversion or duration of seronegative status in a group of 168 HIV exposed individuals, including 74 seroconverters and 94 HESN based on carriage or not of KIR3DL1/S1/HLA-B genotypes previously shown to be associated with protection from infection and/or slow time to AIDS. KIR3DL1/S1 genotyping was performed by sequence-specific primer polymerase chain reaction using two pairs of specific primers for each locus. The MHC class IB locus was typed to four-position resolution to resolve Bw4 and Bw6 alleles and the amino acid present at position 80. KIR3DL1/S1 heterozygotes became HIV infected significantly faster than KIR3DS1 homozygotes. Individuals who carried both KIR3DS1 and Bw4*80I did not remain HIV seronegative longer than those from a control group who were homozygous for HLA-Bw6 and carried no HLA-A locus Bw4 alleles Subjects who were *h/*y+B*57 showed a trend towards slower time to serconversion than those with other KIR3DL1 homozygous and KIR3DL1/S1 heterozygous genotypes. Thus, KIR3DS1 homozygosity is associated with protection from HIV infection while co-carriage of KIR3DS1 and Bw4*80I is not. The requirements for protection from HIV infection can differ from those that influence time to AIDS in HIV infected individuals. Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface killer immunoglobulin-like receptor locus KIR3DL1/S1 have been shown to influence time to AIDS in HIV-infected individuals and risk of seroconversion in HIV exposed seronegative (HESN) subjects. Here, we assessed time to seroconversion or duration of seronegative status in a group of 168 HIV exposed individuals, including 74 seroconverters and 94 HESN based on carriage or not of KIR3DL1/S1/HLA-B genotypes previously shown to be associated with protection from infection and/or slow time to AIDS. KIR3DL1/S1 genotyping was performed by sequence-specific primer polymerase chain reaction using two pairs of specific primers for each locus. The MHC class IB locus was typed to four-position resolution to resolve Bw4 and Bw6 alleles and the amino acid present at position 80. KIR3DL1/S1 heterozygotes became HIV infected significantly faster than KIR3DS1 homozygotes. Individuals who carried both KIR3DS1 and Bw4*80I did not remain HIV seronegative longer than those from a control group who were homozygous for HLA-Bw6 and carried no HLA-A locus Bw4 alleles Subjects who were *h/*y+B*57 showed a trend towards slower time to serconversion than those with other KIR3DL1 homozygous and KIR3DL1/S1 heterozygous genotypes. Thus, KIR3DS1 homozygosity is associated with protection from HIV infection while co-carriage of KIR3DS1 and Bw4*80I is not. The requirements for protection from HIV infection can differ from those that influence time to AIDS in HIV infected individuals.Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface killer immunoglobulin-like receptor locus KIR3DL1/S1 have been shown to influence time to AIDS in HIV-infected individuals and risk of seroconversion in HIV exposed seronegative (HESN) subjects. Here, we assessed time to seroconversion or duration of seronegative status in a group of 168 HIV exposed individuals, including 74 seroconverters and 94 HESN based on carriage or not of KIR3DL1/S1/HLA-B genotypes previously shown to be associated with protection from infection and/or slow time to AIDS. KIR3DL1/S1 genotyping was performed by sequence-specific primer polymerase chain reaction using two pairs of specific primers for each locus. The MHC class IB locus was typed to four-position resolution to resolve Bw4 and Bw6 alleles and the amino acid present at position 80. KIR3DL1/S1 heterozygotes became HIV infected significantly faster than KIR3DS1 homozygotes. Individuals who carried both KIR3DS1 and Bw4*80I did not remain HIV seronegative longer than those from a control group who were homozygous for HLA-Bw6 and carried no HLA-A locus Bw4 alleles Subjects who were *h/*y+B*57 showed a trend towards slower time to serconversion than those with other KIR3DL1 homozygous and KIR3DL1/S1 heterozygous genotypes. Thus, KIR3DS1 homozygosity is associated with protection from HIV infection while co-carriage of KIR3DS1 and Bw4*80I is not. The requirements for protection from HIV infection can differ from those that influence time to AIDS in HIV infected individuals. |
Audience | Academic |
Author | Kiani, Zahra Routy, Jean-Pierre Tan, Xianming Tsoukas, Christos M. Tallon, Benjamin J. M. Bernard, Nicole F. Bruneau, Julie |
AuthorAffiliation | 2 Division of Experimental Medicine, McGill University, Montréal, Québec, Canada 5 Division of Clinical Immunology and Allergy, McGill University Health Centre, Montréal, Québec, Canada 4 Family Medicine Department, Université de Montréal, Montréal, Québec, Canada 3 Centre de recherche, Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, Québec, Canada 1 Research Institute of the McGill University Health Centre (RI MUHC), Montréal, Québec, Canada 7 Biostatistics Core Facility, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada 6 Immunodeficiency Service and Division of Hematology, Royal Victoria Hospital, McGill University Health Centre, Montréal, Québec, Canada Karolinska Institutet, Sweden |
AuthorAffiliation_xml | – name: 6 Immunodeficiency Service and Division of Hematology, Royal Victoria Hospital, McGill University Health Centre, Montréal, Québec, Canada – name: 3 Centre de recherche, Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, Québec, Canada – name: 7 Biostatistics Core Facility, Research Institute of the McGill University Health Centre, Montréal, Québec, Canada – name: Karolinska Institutet, Sweden – name: 4 Family Medicine Department, Université de Montréal, Montréal, Québec, Canada – name: 1 Research Institute of the McGill University Health Centre (RI MUHC), Montréal, Québec, Canada – name: 2 Division of Experimental Medicine, McGill University, Montréal, Québec, Canada – name: 5 Division of Clinical Immunology and Allergy, McGill University Health Centre, Montréal, Québec, Canada |
Author_xml | – sequence: 1 givenname: Benjamin J. M. surname: Tallon fullname: Tallon, Benjamin J. M. – sequence: 2 givenname: Julie surname: Bruneau fullname: Bruneau, Julie – sequence: 3 givenname: Christos M. surname: Tsoukas fullname: Tsoukas, Christos M. – sequence: 4 givenname: Jean-Pierre surname: Routy fullname: Routy, Jean-Pierre – sequence: 5 givenname: Zahra surname: Kiani fullname: Kiani, Zahra – sequence: 6 givenname: Xianming surname: Tan fullname: Tan, Xianming – sequence: 7 givenname: Nicole F. surname: Bernard fullname: Bernard, Nicole F. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25330014$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | COPYRIGHT 2014 Public Library of Science 2014 Tallon et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2014 Tallon et al 2014 Tallon et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: The authors have declared that no competing interests exist. Conceived and designed the experiments: NFB BT. Performed the experiments: BT. Analyzed the data: BT NFB XT ZK. Contributed reagents/materials/analysis tools: JB CMT J-PR. Contributed to the writing of the manuscript: BT JB CMT J-PR ZK XT NFB. |
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Snippet | Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface... Natural killer (NK) cells play a role in the clearance of viral infections. Combinations of alleles at the polymorphic HLA-B locus and the NK cell surface... |
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SubjectTerms | Acquired immune deficiency syndrome Adult AIDS AIDS (Disease) Alleles Amino acids Antigens Biology and life sciences Blood & organ donations Cell surface Exposure Female Genetic aspects Genetic Association Studies Genotype Genotypes Genotyping Haplotypes Health aspects Health risks Heterozygotes Histocompatibility antigen HLA HIV HIV Infections - genetics HIV Infections - immunology HIV Infections - virology HIV Seropositivity - genetics HIV Seropositivity - immunology HIV-1 - genetics HIV-1 - immunology HIV-1 - pathogenicity HLA antigens HLA-A Antigens - genetics HLA-A Antigens - immunology HLA-B Antigens - genetics HLA-B Antigens - immunology Homozygosity Homozygotes Human immunodeficiency virus Humans Immunoglobulins Immunology Infection Infections Killer Cells, Natural - immunology Ligands Loci Major histocompatibility complex Male Medicine Medicine and health sciences Middle Aged Natural killer cells Physical Sciences Polymerase chain reaction Potassium channels (inwardly-rectifying) Primers Receptors, KIR3DL1 - genetics Seroconversion |
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Title | Time to Seroconversion in HIV-Exposed Subjects Carrying Protective versus Non Protective KIR3DS1/L1 and HLA-B Genotypes |
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