4.7 Article

MHC-I-restricted melanoma antigen specific TCR-engineered human CD4+T cells exhibit multifunctional effector and helper responses, in vitro

期刊

CLINICAL IMMUNOLOGY
卷 136, 期 3, 页码 338-347

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2010.04.013

关键词

Cancer immunotherapy; TCR; Multi functional CD4 T cells

资金

  1. PHS [CA 83130, CA 88059, CA 129816]
  2. Dowling Foundation
  3. Samuel Waxman Cancer Research Foundation
  4. W.M. Keck Foundation
  5. Joy and Jerry Monkarsh Fund
  6. Breast Cancer Alliance
  7. Connecticut
  8. GCRC, UCHC [MO 1RR06192]

向作者/读者索取更多资源

MHC class I-restricted human melanoma epitope MART-1(27-35) specific TCR-engineered CD4+CD25- T cells synthesize Th1 type cytokines and exhibit cytolytic effector function upon cognate stimulation. A detailed characterization of such TCR-engineered CD4+CD25- T cells now reveals that they are multifunctional. For example, they undergo multiple rounds of division, synthesize cytokines (IFN-gamma, TNF-alpha, IL-2, and MIP1 beta), lyse target cells, and help the expansion of the MART-1(27-35) specific CD8+ T cells when stimulated by the MART-1(27-35) peptide pulsed DC. Multiparametric analyses reveal that a single TCR-engineered CD4+ T cell can perform as many as five different functions. Nearly 100% MART-1(27-35) specific TCR expressing CD4+ T cells can be generated through retroviral vector-based transduction and one round of in vitro stimulation by the peptide pulsed DC. MHC class I-restricted tumor epitope specific TCR transduced CD4+ T cells, therefore, could be useful in immunotherapeutic strategies for melanoma or other human malignancies. (C) 2010 Elsevier Inc. All rights reserved.

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