HLA-DR-restricted T-cell responses to factor VIII epitopes in a mild haemophilia A family with missense substitution A2201P

被引:44
作者
Ettinger, R. A. [1 ,2 ]
James, E. A. [2 ]
Kwok, W. W. [2 ,3 ]
Thompson, A. R. [1 ,4 ]
Pratt, K. P. [1 ,4 ]
机构
[1] Univ Washington, Puget Sound Blood Ctr, Seattle, WA 98104 USA
[2] Univ Washington, Benaroya Res Inst, Seattle, WA 98104 USA
[3] Univ Washington, Dept Immunol, Seattle, WA 98104 USA
[4] Univ Washington, Dept Med, Div Hematol, Seattle, WA 98104 USA
关键词
epitope mapping; factor VIII inhibitors; haemophilia A; HLA-DR; T-cell; COAGULATION-FACTOR-VIII; MALMO INTERNATIONAL BROTHER; RECOMBINANT FACTOR-VIII; FACTOR-IX INHIBITORS; CRYSTAL-STRUCTURE; C2; DOMAIN; RISK; MUTATIONS; IDENTIFICATION; POLYMORPHISMS;
D O I
10.1111/j.1365-2516.2008.01905.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An HLA-DRA-DRB1 *0101-restricted T-cell epitope in the factor VIII (FVIII) C2 domain occurred in a mild haemophilia A patient with missense substitution FVIII-A2201P. His T cells responded to synthetic peptides FVIII2186-2705 and FVIII2194-2213 (J Thromb Haemost 2007; 5: 2399). T cells from family members with genotype A2201P were analysed to determine if FVIII-specific T cells occur in individuals with a haemophilic mutation but no clinically significant inhibitor response. Fluorescent MHC class II tetramers corresponding to subjects' HLA-DRB1 types were loaded with 20-mer peptides and utilized to label antigen-specific CD4+ T cells. T-cell responses to peptides spanning the FVIII-C2 sequence were evaluated. T cells recognizing specific peptides were cloned, and antigen specificity was verified by proliferation assays. Plasma and/or purified IgG samples were tested for FVIII inhibitory activity. CD4+ T cells and T-cell clones from two brothers who shared the DRB1 *0101 allele responded to FVIII2194-2213. A haemophilic cousin's HLA-DRA-DRB1 *1104-restricted response to FVIII2202-2221 was detected only when CD4+CD25+ cells were depleted. A great uncle and two obligate carriers had no detectable FVIII-C2-specific T cells. Concentrated IgG from the brother without a clinical inhibitor response showed a low-titre FVIII inhibitor. FVIII-specific T cells and inhibitory IgG were found in a previously infused, haemophilic subject who had a sub-clinical FVIII inhibitor. CD4+CD25+ depleted T cells from a non-infused haemophilic cousin recognized an overlapping FVIII epitope, indicating a latent HLA-DRA-DRB1 *1104-restricted T-cell response to FVIII. Specific T-cell responses to FVIII can occur without clinically significant inhibitors.
引用
收藏
页码:44 / 55
页数:12
相关论文
共 59 条
[1]   HISTOCOMPATIBILITY ANTIGEN PATTERNS IN HEMOPHILIC PATIENTS WITH FACTOR-VIII ANTIBODIES [J].
ALY, AM ;
ALEDORT, LM ;
LEE, TD ;
HOYER, LW .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 76 (02) :238-241
[2]   Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A [J].
Astermark, J. ;
Wang, X. ;
Oldenburg, J. ;
Berntorp, E. ;
Lefvert, A. -K. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2007, 5 (02) :263-265
[3]   Basic aspects of inhibitors to factors VIII and IX and the influence of non-genetic risk factors [J].
Astermark, J. .
HAEMOPHILIA, 2006, 12 :8-13
[4]   Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A [J].
Astermark, J ;
Oldenburg, J ;
Pavlova, A ;
Berntorp, E ;
Lefvert, AK .
BLOOD, 2006, 107 (08) :3167-3172
[5]   Malmo International Brother Study (MIBS): An international survey of brother pairs with haemophilia [J].
Astermark, J ;
Berntorp, E .
VOX SANGUINIS, 1999, 77 :80-82
[6]   The Malmo International Brother Study (MIBS): further support for genetic predisposition to inhibitor development [J].
Astermark, J ;
Berntorp, E ;
White, GC ;
Kroner, BL .
HAEMOPHILIA, 2001, 7 (03) :267-272
[7]   Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A [J].
Astermark, Jan ;
Oldenburg, Johannes ;
Carlson, Joyce ;
Pavlova, Anna ;
Kavakli, Kaan ;
Berntorp, Erik ;
Lefvert, Ann-Kari .
BLOOD, 2006, 108 (12) :3739-3745
[8]  
Astermark J, 2005, HAEMATOLOGICA, V90, P924
[9]  
Brackmann H-H, 2003, Hamostaseologie, V23, P24
[10]   LOSS OF HIGH-RESPONDER INHIBITORS IN PATIENTS WITH SEVERE HEMOPHILIA-A AND HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION - A REPORT FROM THE MULTICENTER HEMOPHILIA COHORT STUDY [J].
BRAY, GL ;
KRONER, BL ;
ARKIN, S ;
ALEDORT, LW ;
HILGARTNER, MW ;
EYSTER, ME ;
RAGNI, MV ;
GOEDERT, JJ .
AMERICAN JOURNAL OF HEMATOLOGY, 1993, 42 (04) :375-379