Journal article
A long, naturally presented immunodominant epitope from NY-ESO-1 tumor antigen: Implications for cancer vaccine design
LM Ebert, CL Yu, CS Clements, NC Robson, HM Jackson, JL Markby, N Dimopoulos, ST Bee, IF Luescher, ID Davis, J Rossjohn, J Cebon, AW Purcell, W Chen
Cancer Research | AMER ASSOC CANCER RESEARCH | Published : 2009
Abstract
The tumor antigen NY-ESO-1 is a promising cancer vaccine target. We describe here a novel HLA-B7-restricted NY-ESO-1 epitope, encompassing amino acids 60-72 (APRGPHGGAASGL), which is naturally presented by melanoma cells. The tumor epitope bound to HLA-B7 by bulging outward from the peptide-binding cleft. This bulged epitope was not an impediment to T-cell recognition, however, because four of six HLA-B7+ melanoma patients vaccinated with NY-ESO-1 ISCOMATRIX vaccine generated a potent T-cell response to this determinant. Moreover, the response to this epitope was immunodominant in three of these patients and, unlike the T-cell responses to bulged HLA class I viral epitopes, the responding T ..
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Awarded by National Health and Medical Research Council (NHMRC)
Awarded by Cancer Council Victoria
Funding Acknowledgements
National Health and Medical Research Council (NHMRC) project grants 433608 (W. Chen), 491117 (A.W. Purcell and J. Rossjohn), and grants from Cancer Council Victoria 381409 (W. Chen) and 433626 (L. E). J. Rossjohn is an ARC Federation Fellow; C.S. Clements is an ARC QEII fellow and A.W. Purcell is a NHMRC Senior Research Fellow.