The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mullins, D. W.
Right arrow Articles by Engelhard, V. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mullins, D. W.
Right arrow Articles by Engelhard, V. H.
The Journal of Immunology, 2001, 167: 4853-4860.
Copyright © 2001 by The American Association of Immunologists

Immune Responses to the HLA-A*0201-Restricted Epitopes of Tyrosinase and Glycoprotein 100 Enable Control of Melanoma Outgrowth in HLA-A*0201-Transgenic Mice1

David W. Mullins, Timothy N. J. Bullock, Teresa A. Colella, Valentina V. Robila and Victor H. Engelhard2

Department of Microbiology and Carter Immunology Center, University of Virginia, Charlottesville, VA 22908

Many of the Ags recognized by human melanoma-reactive CTL are derived from proteins that are also expressed in melanocytes. The possibility of self-tolerance to these epitopes has led to questions about their utility for antitumor immunotherapy. To investigate the issue, we established a preclinical model based on transgenic mice expressing a recombinant HLA-A*0201 molecule and B16 melanoma transfected to express this molecule. HLA-A*0201-restricted epitopes from the melanocyte differentiation proteins (MDP) tyrosinase and gp100 are expressed in both tumor cells and melanocytes, and the former is associated with self-tolerance. However, adoptive transfer of tyrosinase or gp100-reactive CTL developed from tolerant mice delayed tumor outgrowth, as did immunization with MDP peptide-pulsed dendritic cells. Protection was enhanced by the use of peptide ligands containing conservative substitutions that were cross-reactive with the original Ags. These data establish that CTL populations reactive against MDP-derived self-Ags can be activated to mount effective antitumor immunity and strongly support their continued development for tumor immunotherapy in humans.




This article has been cited by other articles:


Home page
J. Immunol.Home page
R. Lengagne, S. Graff-Dubois, M. Garcette, L. Renia, M. Kato, J.-G. Guillet, V. H. Engelhard, M.-F. Avril, J.-P. Abastado, and A. Prevost-Blondel
Distinct Role for CD8 T Cells toward Cutaneous Tumors and Visceral Metastases
J. Immunol., January 1, 2008; 180(1): 130 - 137.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
L. A. Nichols, Y. Chen, T. A. Colella, C. L. Bennett, B. E. Clausen, and V. H. Engelhard
Deletional Self-Tolerance to a Melanocyte/Melanoma Antigen Derived from Tyrosinase Is Mediated by a Radio-Resistant Cell in Peripheral and Mesenteric Lymph Nodes
J. Immunol., July 15, 2007; 179(2): 993 - 1003.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
S. L. Sheasley-O'Neill, C. C. Brinkman, A. R. Ferguson, M. C. Dispenza, and V. H. Engelhard
Dendritic Cell Immunization Route Determines Integrin Expression and Lymphoid and Nonlymphoid Tissue Distribution of CD8 T Cells
J. Immunol., February 1, 2007; 178(3): 1512 - 1522.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
K. M. Hargadon, C. C. Brinkman, S. L. Sheasley-O'Neill, L. A. Nichols, T. N. J. Bullock, and V. H. Engelhard
Incomplete Differentiation of Antigen-Specific CD8 T Cells in Tumor-Draining Lymph Nodes
J. Immunol., November 1, 2006; 177(9): 6081 - 6090.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
A. D. Gritzapis, L. G. Mahaira, S. A. Perez, N. T. Cacoullos, M. Papamichail, and C. N. Baxevanis
Vaccination with Human HER-2/neu (435-443) CTL Peptide Induces Effective Antitumor Immunity against HER-2/neu-Expressing Tumor Cells In vivo.
Cancer Res., May 15, 2006; 66(10): 5452 - 5460.
[Abstract] [Full Text] [PDF]


Home page
JEMHome page
E. Galkina, A. Kadl, J. Sanders, D. Varughese, I. J. Sarembock, and K. Ley
Lymphocyte recruitment into the aortic wall before and during development of atherosclerosis is partially L-selectin dependent
J. Exp. Med., May 15, 2006; 203(5): 1273 - 1282.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
D. W. Mullins and V. H. Engelhard
Limited infiltration of exogenous dendritic cells and naive T cells restricts immune responses in peripheral lymph nodes.
J. Immunol., April 15, 2006; 176(8): 4535 - 4542.
[Abstract] [Full Text] [PDF]


Home page
JEMHome page
N. Casares, M. O. Pequignot, A. Tesniere, F. Ghiringhelli, S. Roux, N. Chaput, E. Schmitt, A. Hamai, S. Hervas-Stubbs, M. Obeid, et al.
Caspase-dependent immunogenicity of doxorubicin-induced tumor cell death
J. Exp. Med., December 19, 2005; 202(12): 1691 - 1701.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
P. J. Tacken, I. J. M. de Vries, K. Gijzen, B. Joosten, D. Wu, R. P. Rother, S. J. Faas, C. J. A. Punt, R. Torensma, G. J. Adema, et al.
Effective induction of naive and recall T-cell responses by targeting antigen to human dendritic cells via a humanized anti-DC-SIGN antibody
Blood, August 15, 2005; 106(4): 1278 - 1285.
[Abstract] [Full Text] [PDF]


Home page
JEMHome page
D. W. Mullins, S. L. Sheasley, R. M. Ream, T. N.J. Bullock, Y.-X. Fu, and V. H. Engelhard
Route of Immunization with Peptide-pulsed Dendritic Cells Controls the Distribution of Memory and Effector T Cells in Lymphoid Tissues and Determines the Pattern of Regional Tumor Control
J. Exp. Med., October 6, 2003; 198(7): 1023 - 1034.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 2001 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 2001 by The American Association of Immunologists, Inc. All rights reserved.