抗原
主要组织相容性复合体
生物
人类白细胞抗原
抗原处理
次要组织相容性抗原
MHC I级
基因
免疫学
川东北74
遗传学
分子生物学
作者
Rong‐Fu Wang,Xiang Wang,Alicia C. Atwood,Suzanne L. Topalian,Steven A. Rosenberg
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1999-05-21
卷期号:284 (5418): 1351-1354
被引量:300
标识
DOI:10.1126/science.284.5418.1351
摘要
In an effort to identify tumor-specific antigens recognized by CD4(+) T cells, an approach was developed that allows the screening of an invariant chain-complementary DNA fusion library in a genetically engineered cell line expressing the essential components of the major histocompatibility complex (MHC) class II processing and presentation pathway. This led to the identification of a mutated form of human CDC27, which gave rise to an HLA-DR4-restricted melanoma antigen. A mutated form of triosephosphate isomerase, isolated by a biochemical method, was also identified as an HLA-DR1-restricted antigen. Thus, this approach may be generally applicable to the identification of antigens recognized by CD4(+) T cells, which could aid the development of strategies for the treatment of patients with cancer, autoimmune diseases, or infectious diseases.
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