Long-term in vivo provision of antigen-specific T cell immunity by programming hematopoietic stem cells

Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4518-23. doi: 10.1073/pnas.0500600102. Epub 2005 Mar 9.


A method to genetically program mouse hematopoietic stem cells to develop into functional CD8 or CD4 T cells of defined specificity in vivo is described. For this purpose, a bicistronic retroviral vector was engineered that efficiently delivers genes for both alpha and beta chains of T cell receptor (TCR) to hematopoietic stem cells. When modified cell populations were used to reconstruct the hematopoietic lineages of recipient mice, significant percentages of antigen-specific CD8 or CD4 T cells were observed. These cells expressed normal surface markers and responded to peptide antigen stimulation by proliferation and cytokine production. Moreover, they could mature into memory cells after peptide stimulation. Using TCRs specific for a model tumor antigen, we found that the recipient mice were able to partially resist a challenge with tumor cells carrying the antigen. By combining cells modified with CD8- and CD4-specific TCRs, and boosting with dendritic cells pulsed with cognate peptides, complete suppression of tumor could be achieved and even tumors that had become established would regress and be eliminated after dendritic cell/peptide immunization. This methodology of "instructive immunotherapy" could be developed for controlling the growth of human tumors and attacking established pathogens.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, Neoplasm / administration & dosage
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Differentiation
  • Cell Line, Tumor
  • Chickens
  • Dendritic Cells / immunology
  • Female
  • Genes, RAG-1
  • Genetic Vectors
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / immunology*
  • Humans
  • Immunity, Cellular
  • Immunotherapy
  • In Vitro Techniques
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Neoplasms, Experimental / immunology
  • Neoplasms, Experimental / therapy
  • Ovalbumin / immunology
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology*


  • Antigens, Neoplasm
  • Receptors, Antigen, T-Cell, alpha-beta
  • Ovalbumin