S
Siona Eliyahu
Researcher at National Institutes of Health
Publications - 8
Citations - 4440
Siona Eliyahu is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Antigen & Melanoma. The author has an hindex of 7, co-authored 8 publications receiving 4343 citations.
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Journal ArticleDOI
Cloning of the gene coding for a shared human melanoma antigen recognized by autologous T cells infiltrating into tumor.
Yutaka Kawakami,Siona Eliyahu,Cynthia H. Delgado,Paul F. Robbins,Licia Rivoltini,Suzanne L. Topalian,Toru Miki,Steven A. Rosenberg +7 more
TL;DR: A gene encoding a melanocyte lineage-specific protein (MART-1) that is a widely shared melanoma antigen recognized by the T lymphocytes of patients with established malignancy is identified and opens possibilities for the development of immunotherapies for patients with melanoma.
Journal ArticleDOI
Identification of a human melanoma antigen recognized by tumor-infiltrating lymphocytes associated with in vivo tumor rejection.
Yutaka Kawakami,Siona Eliyahu,Cynthia H. Delgado,Paul F. Robbins,Kazuyasu Sakaguchi,Ettore Appella,John R. Yannelli,G J Adema,Toru Miki,Steven A. Rosenberg +9 more
TL;DR: Since the administration of TIL1200 plus interleukin 2 resulted in regression of metastatic cancer in the autologous patient, gp100 is a possible tumor rejection antigen and may be useful for the development of immunotherapies for patients with melanoma.
Journal ArticleDOI
Identification of the immunodominant peptides of the MART-1 human melanoma antigen recognized by the majority of HLA-A2-restricted tumor infiltrating lymphocytes.
Yutaka Kawakami,Siona Eliyahu,Kazuyasu Sakaguchi,Paul F. Robbins,Licia Rivoltini,John R. Yannelli,Ettore Appella,Steven A. Rosenberg +7 more
TL;DR: One of the 9-mer peptides, AAGIGILTV, was most effective in sensitizing the T2 cells for TIL lysis and appears to be a very common immunogenic epitope for HLA-A2-restricted melanoma-specific TIL and may be useful for the development of immunotherapeutic strategies.
Journal ArticleDOI
Wild-type p53 can inhibit oncogene-mediated focus formation.
TL;DR: The effects of plasmids encoding wild-type (wt) p53 on the ability of primary rat embryo fibroblasts to be transformed by a combination of mutant p53 and ras support the notions that wt p53 expression may be restrictive to neoplastic progression and that p53 inactivation may play a crucial role in tumorigenesis.
Journal Article
Recognition of multiple epitopes in the human melanoma antigen gp100 by tumor-infiltrating T lymphocytes associated with in vivo tumor regression.
Yutaka Kawakami,Siona Eliyahu,C. Jennings,Kazuyasu Sakaguchi,Xiaoqiang Kang,Scott Southwood,Paul F. Robbins,Alessandro Sette,Ettore Appella,Steven A. Rosenberg +9 more
TL;DR: Four of ten HLA-A2-restricted melanoma specific CTL that were derived from tumor-infiltrating lymphocytes (TIL) and administered to patients recognized the gp100 melanoma Ag and nine of ten recognized the MART-1 Ag.