TY - JOUR
T1 - Cloning genes encoding MHC class II-restricted antigens
T2 - Mutated CDC27 as a tumor antigen
AU - Wang, Rong Fu
AU - Wang, Xiang
AU - Atwood, Alicia C.
AU - Topalian, Suzanne L.
AU - Rosenberg, Steven A.
PY - 1999/5/21
Y1 - 1999/5/21
N2 - 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.
AB - 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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U2 - 10.1126/science.284.5418.1351
DO - 10.1126/science.284.5418.1351
M3 - Article
C2 - 10334988
AN - SCOPUS:0033591429
SN - 0036-8075
VL - 284
SP - 1351
EP - 1354
JO - Science
JF - Science
IS - 5418
ER -