ライフサイエンスコーパス: melanoma antigen

1 F6 and expressing a transgenic TCR for gp100-melanoma antigen.

2 27, which gave rise to an HLA-DR4-restricted melanoma antigen.

3 ization to the human MART-1/Melan-A (MART-1) melanoma antigen.

4 RA by downregulating expression of PRAME, a melanoma antigen.

5 ization with a post-translationally modified melanoma antigen.

6 ng gp100 and CTL clones specific for a gp100 melanoma antigen.

7 stricted peptides derived from either HIV or melanoma antigens.

8 r Ags, including melanoma-associated Ag 1, B melanoma antigen 1, and Wilm tumor Ag 1.

9 screen, we identified an interaction between melanoma antigen-11 (MAGE-11) cancer-testis antigen and

10 A variety of melanoma antigen A (MAGE-A) genes are commonly detected

11 The menstrual cycle-dependent expression of melanoma antigen-A11 (MAGE-11) in the mid-secretory huma

12 (N/C) interaction enables direct binding to melanoma antigen-A11 (MAGE-11), an AR coregulator that i

13 X-linked primate-specific melanoma antigen-A11 (MAGE-A11) is a human androgen rece

14 Melanoma antigen-A11 (MAGE-A11) is a low-abundance, prim

15 rimate-specific steroid receptor coregulator melanoma antigen-A11 (MAGE-A11).

16 AR WXXLF motif (433)WHTLF(437) required for melanoma antigen-A11 and p300 to stimulate transcription

17 We conclude that the coregulator effects of melanoma antigen-A11 on the AR NH(2)- and carboxyl-termi

18 ys that depend on the coregulator effects of melanoma antigen-A11.

19 Here we identify the cancer/testes antigen melanoma antigen-A4 (MAGE-A4) as a tumour cell-specific

20 Melanoma antigen-A4 (MAGE-A4), a cancer-testis antigen,

21 ptide derived from the cancer testis antigen melanoma antigen-A4 (MAGE-A4).

22 is study, we investigated a small library of melanoma antigens and the effects of several formulation

23 , oncogenesis (TGFbeta1, cathepsin L, IGFR1, melanoma antigen) and apoptosis (Bcl-2, Bid, Bad, p53) a

24 The GM2 ganglioside is a well-defined melanoma antigen, and anti-GM2 antibodies have been asso

25 Whereas many of the identified human melanoma antigens are normal tissue differentiation prot

26 When analyzing T-cell recognition of shared melanoma antigens before and after adoptive cell therapy

27 As expected, early on-target recognition of melanoma antigens by tumor-specific CD4(+) T cells was r

28 expressed the CT antigen CT7 (also known as melanoma antigen C1 [MAGE-C1]) and 70% expressed MAGE-A3

29 s or enhances T cell function in response to melanoma antigens, depending on the dose of drug in the

30 ein-1 and -2 (TRP-1 and TRP-2), gp100, human melanoma antigen-encoding genes 1 and 3 (MAGE-1 and MAGE

31 lanoma-specific CTL precursors that can kill melanoma antigen-expressing targets.

32 with exogenous peptides or transduction with melanoma antigen-expressing viruses.

33 ed, and four active compounds that increased melanoma antigen expression leading to enhanced IFNgamma

34 Necdin, a melanoma antigen family protein, promotes neuronal and m

35 GABAA) receptor gene family, a member of the melanoma antigen gene (MAGE) family, and several members

36 MageB2 belongs to the melanoma antigen gene (MAGE-I) family of tumor-specific

37 In all of the CSAGE positive samples, the melanoma antigen gene family was also expressed.

38 eport, we identified the X chromosome-linked melanoma antigen gene product MAGE-11 as an AR coregulat

39 Melanoma antigen gene protein 11 (MAGE-11) is an AR core

40 interactions is supported by the effects of melanoma antigen gene protein-11, an AR coregulator that

41 In humans and other primates, melanoma antigen gene protein-A11 (MAGE-11) is an AR sel

42 with coregulatory proteins that include the melanoma antigen gene protein-A11 (MAGE-11).

43 ognized by T cells-1 (MART-1), and universal melanoma antigen gene-A (uMAG-A).

44 (antigen recognized by T cells-1), MAGE-A3 (melanoma antigen gene-A3 family), GalNAc-T (beta1-->4-N-

45 ox homeotic gene transcription factor 3; and melanoma antigen gene-A3 family, and the changes of CTCs

46 endritic cells (DCs) engineered to express a melanoma antigen generates antigen-specific, MHC-restric

47 of dendritic cells (DCs) expressing a model melanoma antigen generates antigen-specific, MHC-restric

48 both the target antigen Tyrp1 and a distinct melanoma antigen gp100 in an Fc receptor-dependent mecha

49 s recognize an epitope derived from the self/melanoma antigen gp100.

50 ioma cell lines (GL26 and GL261) express the melanoma antigens gp100 and tyrosinase-related protein 2

51 ssional antigen-presenting cells loaded with melanoma antigens gp100 and tyrosinase.

52 enhances DNA vaccination against a distinct melanoma antigen, gp100(pmel17/silver locus), improving

53 c cells loaded with peptide derived from the melanoma antigen, gp100, failed to mediate regression of

54 e (amino acids 209-217) derived from a human melanoma antigen, gp100.

55 Characterization of immunogenic human melanoma antigens has been a major focus of tumor immuno

56 cells specific for idealized or established melanoma antigens in mice.

57 NRAGE (neurotrophin receptor-interacting melanoma antigen) interacted with a component of the E-c

58 llectively, this study links three important melanoma antigens into a common transcriptional pathway

59 ults suggest engineering macrophages against melanoma antigens is a promising solid tumor immunothera

60 Cytotoxic T lymphocyte priming towards melanoma antigens is also obtained with cells from metas

61 ass I molecules, we hypothesized that mature melanoma antigen-loaded DCs engineered to process antige

62 The melanoma antigen (MAGE) family consists of more than 60

63 Type I melanoma antigen (MAGE) family members are detected in n

64 Melanoma antigen (MAGE) genes are conserved in all eukar

65 The melanoma antigen (MAGE) proteins all contain a MAGE homo

66 Testis-restricted melanoma antigen (MAGE) proteins are frequently hijacked

67 D27(+)CD8(+) T cells against the four shared melanoma antigens: MAGE-3, gp100, tyrosinase, and MART-1

68 ity T-cell receptors (TCRalpha/beta) for the melanoma antigen MART-1/HLA-A*0201 [recognized by F5 cyt

69 DMF5, a T-cell receptor that recognizes the melanoma antigen MART-127-35 (DMF5(TLR5L) T cells), disp

70 th mature DCs transfected with RNAs encoding melanoma antigens MART1, MAGE-3, gp100, and tyrosinase.

71 ing DC vaccines expressing three full-length melanoma antigens (MAs) was performed.

72 were pulsed with peptides derived from four melanoma antigens [(MelAgs) MelanA/MART-1, tyrosinase, M

73 s were stained with hematoxylin-eosin (H-E), melanoma antigen (melan-A), and again with H-E.

74 by using cells raised against the candidate melanoma antigen mutant B-Raf or its phosphorylated coun

75 tion between the class II epitope-containing melanoma antigen New York esophageal 1 and MHC class II.

76 activated B cells to stimulate T cells using melanoma antigens or melanoma cell lysates.

77 sion and led to endogenous responses against melanoma antigens other than NY-ESO-1.

78 d tyrosinase-related protein-2 (TRP-2), is a melanoma antigen overexpressed in most chemo-/radiothera

79 te antigen (HLA) class I antigen-restricted, melanoma antigen-reactive T-cell receptors; however, sub

80 e, we describe the identification of a novel melanoma antigen recognized by an human histocompatibili

81 s the melanoma-associated antigens gp100 and melanoma antigen recognized by T cells (MART-1).

82 d frequency of gp100 and T cells specific to melanoma antigen recognized by T cells 1 (MART-1), also

83 se (TYR), TYR-related protein 2 (TRP-2), and melanoma antigen recognized by T cells 1 (MART-1); all t

84 abeled with human melanoma black 45 (HMB45), melanoma antigen recognized by T cells 1 (Melan-A), S100

85 ression of four melanoma-associated markers: melanoma antigen recognized by T cells 1; beta1 --> 4-N-

86 by MM-RT-PCR, using the markers tyrosinase, melanoma antigen recognized by T cells-1 (MART-1), and u

87 l structure of a phosphopeptide derived from melanoma antigen recognized by T cells-1 (pMART-1), sele

88 33%, 5%, and 13% (negative) for tyrosinase, melanoma antigen recognized by T cells-1, tyrosinase-rel

89 This protein has been identified as a melanoma antigen recognized by tumor reactive CTLs deriv

90 Autologous dendritic cells pulsed with the melanoma antigen recognized T cells 1 self-peptide were

91 ss in the structural identification of human melanoma antigens recognized by autologous cytotoxic T c

92 Several epitopes in the human melanoma antigens recognized by HLA-A2-restricted CTLs h

93 , DCT (tyrosinase-related protein 2), MART1 (melanoma antigens recognized by T-cells) gp100 (Pmel17/s

94 are able to prime an immune response against melanoma antigens shared between K1735 and B16.

95 clonotypes specific for public overexpressed melanoma antigens (shared across different tumours) or p

96 lymphocytes (TIL), including MART-1/Melan-A melanoma antigen-specific CD8 T cells, predominantly exp

97 in tumor-draining lymph nodes, and increased melanoma antigen-specific CD8(+) T cells in the spleen.

98 inflammatory responses and the production of melanoma antigen-specific CD8(+) T cells.

99 tudinal phenotypic analysis was performed on melanoma antigen-specific CD8+ T cells during their tran

100 of Akt, resistance to cell death induced by melanoma antigen-specific cytotoxic T cells, and phospha

101 re not recognized by HLA class I-restricted, melanoma antigen-specific cytotoxic T lymphocytes even f

102 or LAQ824 and the adoptive transfer of gp100 melanoma antigen-specific pmel-1 T cells.

103 In melanoma antigen-specific T cells, CO-induced transient

104 ogous gene-modified lymphocytes expressing a melanoma antigen-specific TCR at the National Cancer Ins

105 and not by CTL specific for more traditional melanoma antigens such as TRP2 or gp100.

106 ector T cells specific for either EBNA1 or a melanoma antigen, suggesting that these CD4(+) Treg cell

107 Recent studies have identified new melanoma antigens that are recognised by CD4(+) T cells.

108 to be due to an immune response generated to melanoma antigens that cross-react with normal skin.

109 then trans-fected with RNA encoding defined melanoma antigens, these DCs were superior inducers of a

110 ass I MHC (HLA-A2)-restricted epitope of the melanoma antigen tyrosinase was isolated from a CD4(+) t

111 artic acid to an isoaspartic acid within the melanoma antigen tyrosinase-related protein (TRP)-2 pept

112 rophylactic prime-boost vaccination with the melanoma antigen tyrosinase-related protein 2, which als

113 ice bearing a TCR transgene specific for the melanoma antigen tyrosinase-related protein-2 (TRP-2, Dc

114 isteria monocytogenes vaccine expressing the melanoma antigen tyrosinase-related protein-2 to protect

115 nsfer of genes encoding TCRs recognizing the melanoma antigen tyrosinase.

116 ma patients were immunized against the gp100 melanoma antigen using autologous peptide-pulsed, CD40L/

117 Interestingly, T cells specific to melanoma antigens were generated.

118 otein of 113 kDa, originally identified as a melanoma antigen, whose expression is associated with tu