The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.

OBJECTIVES: HLA-B*27:05 is associated with AS whereas HLA-B*27:09 is not associated. We hypothesized that different interactions with KIR immune receptors could contribute to the difference in disease association between HLA-B*27:05 and HLAB*27:09. Thus, the objective of this study was to compare th...

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Κύριοι συγγραφείς: Cauli, A, Shaw, J, Giles, J, Hatano, H, Rysnik, O, Payeli, S, McHugh, K, Dessole, G, Porru, G, Desogus, E, Fiedler, S, Hölper, S, Carette, A, Blanco-Gelaz, M, Vacca, A, Piga, M, Ibba, V, Garau, P, La Nasa, G, López-Larrea, C, Mathieu, A, Renner, C, Bowness, P, Kollnberger, S
Μορφή: Journal article
Γλώσσα:English
Έκδοση: Oxford University Press 2013
_version_ 1826288903731019776
author Cauli, A
Shaw, J
Giles, J
Hatano, H
Rysnik, O
Payeli, S
McHugh, K
Dessole, G
Porru, G
Desogus, E
Fiedler, S
Hölper, S
Carette, A
Blanco-Gelaz, M
Vacca, A
Piga, M
Ibba, V
Garau, P
La Nasa, G
López-Larrea, C
Mathieu, A
Renner, C
Bowness, P
Kollnberger, S
author_facet Cauli, A
Shaw, J
Giles, J
Hatano, H
Rysnik, O
Payeli, S
McHugh, K
Dessole, G
Porru, G
Desogus, E
Fiedler, S
Hölper, S
Carette, A
Blanco-Gelaz, M
Vacca, A
Piga, M
Ibba, V
Garau, P
La Nasa, G
López-Larrea, C
Mathieu, A
Renner, C
Bowness, P
Kollnberger, S
author_sort Cauli, A
collection OXFORD
description OBJECTIVES: HLA-B*27:05 is associated with AS whereas HLA-B*27:09 is not associated. We hypothesized that different interactions with KIR immune receptors could contribute to the difference in disease association between HLA-B*27:05 and HLAB*27:09. Thus, the objective of this study was to compare the formation of β2m-free heavy chain (FHC) including B27 dimers (B272) by HLA-B*27:05 and HLA-B*27:09 and their binding to KIR immunoreceptors. METHODS: We studied the formation of HLA-B*27:05 and HLA-B*27:09 heterotrimers and FHC forms including dimers in vitro and in transfected cells. We investigated HLA-B*27:05 and HLA-B*27:09 binding to KIR3DL1, KIR3DL2 and LILRB2 by FACS staining with class I tetramers and by quantifying interactions with KIR3DL2CD3ε-reporter cells and KIR3DL2-expressing NK cells. We also measured KIR expression on peripheral blood NK and CD4 T cells from 18 HLA-B*27:05 AS patients, 8 HLA-B27 negative and 12 HLA-B*27:05+ and HLA-B*27:09+ healthy controls by FACS staining. RESULTS: HLA-B*27:09 formed less B27₂ and FHC than HLA-B*27:05. HLA-B*27:05-expressing cells stimulated KIR3DL2CD3ε-reporter T cells more effectively. Cells expressing HLA-B*27:05 promoted KIR3DL2+ NK cell survival more strongly than HLA-B*27:09. HLA-B*27:05 and HLA-B*27:09 dimer tetramers stained KIR3DL1, KIR3DL2 and LILRB2 equivalently. Increased proportions of NK and CD4 T cells expressed KIR3DL2 in HLA-B*27:05+ AS patients compared with HLA-B*27:05+, HLA-B*27:09+ and HLA-B27- healthy controls. CONCLUSION: Differences in the formation of FHC ligands for KIR3DL2 by HLA-B*27:05 and HLA-B*27:09 could contribute to the differential association of these alleles with AS.
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spelling oxford-uuid:a3d3c09d-988c-49eb-a6cd-2fb33ec0266a2022-03-27T02:29:51ZThe arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a3d3c09d-988c-49eb-a6cd-2fb33ec0266aEnglishSymplectic Elements at OxfordOxford University Press2013Cauli, AShaw, JGiles, JHatano, HRysnik, OPayeli, SMcHugh, KDessole, GPorru, GDesogus, EFiedler, SHölper, SCarette, ABlanco-Gelaz, MVacca, APiga, MIbba, VGarau, PLa Nasa, GLópez-Larrea, CMathieu, ARenner, CBowness, PKollnberger, SOBJECTIVES: HLA-B*27:05 is associated with AS whereas HLA-B*27:09 is not associated. We hypothesized that different interactions with KIR immune receptors could contribute to the difference in disease association between HLA-B*27:05 and HLAB*27:09. Thus, the objective of this study was to compare the formation of β2m-free heavy chain (FHC) including B27 dimers (B272) by HLA-B*27:05 and HLA-B*27:09 and their binding to KIR immunoreceptors. METHODS: We studied the formation of HLA-B*27:05 and HLA-B*27:09 heterotrimers and FHC forms including dimers in vitro and in transfected cells. We investigated HLA-B*27:05 and HLA-B*27:09 binding to KIR3DL1, KIR3DL2 and LILRB2 by FACS staining with class I tetramers and by quantifying interactions with KIR3DL2CD3ε-reporter cells and KIR3DL2-expressing NK cells. We also measured KIR expression on peripheral blood NK and CD4 T cells from 18 HLA-B*27:05 AS patients, 8 HLA-B27 negative and 12 HLA-B*27:05+ and HLA-B*27:09+ healthy controls by FACS staining. RESULTS: HLA-B*27:09 formed less B27₂ and FHC than HLA-B*27:05. HLA-B*27:05-expressing cells stimulated KIR3DL2CD3ε-reporter T cells more effectively. Cells expressing HLA-B*27:05 promoted KIR3DL2+ NK cell survival more strongly than HLA-B*27:09. HLA-B*27:05 and HLA-B*27:09 dimer tetramers stained KIR3DL1, KIR3DL2 and LILRB2 equivalently. Increased proportions of NK and CD4 T cells expressed KIR3DL2 in HLA-B*27:05+ AS patients compared with HLA-B*27:05+, HLA-B*27:09+ and HLA-B27- healthy controls. CONCLUSION: Differences in the formation of FHC ligands for KIR3DL2 by HLA-B*27:05 and HLA-B*27:09 could contribute to the differential association of these alleles with AS.
spellingShingle Cauli, A
Shaw, J
Giles, J
Hatano, H
Rysnik, O
Payeli, S
McHugh, K
Dessole, G
Porru, G
Desogus, E
Fiedler, S
Hölper, S
Carette, A
Blanco-Gelaz, M
Vacca, A
Piga, M
Ibba, V
Garau, P
La Nasa, G
López-Larrea, C
Mathieu, A
Renner, C
Bowness, P
Kollnberger, S
The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.
title The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.
title_full The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.
title_fullStr The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.
title_full_unstemmed The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.
title_short The arthritis-associated HLA-B*27:05 allele forms more cell surface B27 dimer and free heavy chain ligands for KIR3DL2 than HLA-B*27:09.
title_sort arthritis associated hla b 27 05 allele forms more cell surface b27 dimer and free heavy chain ligands for kir3dl2 than hla b 27 09
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