Preferential HLA usage in the influenza virus-specific CTL response

被引:45
作者
Boon, ACM
de Mutsert, G
Fouchier, RAM
Sintnicolaas, K
Osterhaus, ADME
Rimmelzwaan, GF
机构
[1] Erasmus Univ, Med Ctr, Inst Virol, Dept Virol, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, World Hlth Org Natl Influenza Ctr, NL-3000 DR Rotterdam, Netherlands
[3] Sanquin Bloodbank Rotterdam, Lab Histocompatibil & Immunogenet, Dordrecht, Netherlands
关键词
D O I
10.4049/jimmunol.172.7.4435
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To study whether individual HLA class I alleles are used preferentially or equally in human virus-specific CTL responses, the contribution of individual HLA-A and -B alleles to the human influenza virus-specific CTL response was investigated. To this end, PBMC were obtained from three groups of HLA-A and -B identical blood donors and stimulated with influenza virus. In the virus-specific CD8(+) T cell population, the proportion of IFN-gamma- and TNF-alpha-producing cells, restricted by individual HLA-A and -B alleles, was determined using virus-infected C1R cells expressing a single HLA-A or -B allele for restimulation of these cells. In HLA-B*2705- and HLA-B*3501-positive individuals, these alleles were preferentially used in the influenza A virus-specific CTL response, while the contribution of HLA-B*0801 and HLA-A*0101 was minor in these donors. The magnitude of the HLA-B*0801-restricted response was even lower in the presence of HLA-B*2705. OR cells expressing HLA-B*2705, HLA-A*0101, or HLA-A*0201 were preferentially lysed by virus-specific CD8+ T cells. In contrast, the CTL response to influenza B virus was mainly directed toward HLA-B*0801-restricted epitopes. Thus, the preferential use of HLA alleles depended on the virus studied.
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页码:4435 / 4443
页数:9
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