Regulating MHC expression for cellular therapeutics

Transfusion. 2007 Jan;47(1):18-27. doi: 10.1111/j.1537-2995.2007.01059.x.

Abstract

Background: In the past decade, regenerative medicine and cell-based therapies have emerged as new science and technology, with the main goal of repairing, replacing, or regenerating new tissues. A critical issue in this field is the high polymorphism of HLA, which compromises immune acceptance. The lentivirus-mediated delivery of short-hairpin RNAs (shRNAs) has proved to be an efficient method to inhibit the translation of a specific gene.

Study design and methods: A lentiviral-based vector system was used for drug-inducible expression of shRNA sequences that target either beta2-microglobulin (beta2m) or HLA heavy-chain transcripts.

Results: The transduction of inducible RNA interference cassettes containing the sequences for shRNAs targeting beta2m or HLA heavy chain suppressed HLA class I expression by up to 90 percent in HeLa and B-lymphocyte cell lines as well as in peripheral blood monocytes. The expression of HLA class I antigens was fully restored in these cells after the drug had been discontinued. It was demonstrated that HLA class I knockdown was effective in preventing antibody-mediated cell lysis and CD8+ T-cell response. The residual HLA expression in HLA-silenced cells may provide sufficient protection against natural killer cell-mediated lysis.

Conclusions: These data demonstrate the feasibility of controlling HLA expression by genetically modifying cell-based therapeutics to overcome the limitations of immune rejection, bringing cellular therapies closer to reality.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Line, Transformed
  • Cell Proliferation
  • Complement System Proteins / immunology
  • Cytotoxicity Tests, Immunologic
  • Feasibility Studies
  • Gene Transfer Techniques
  • Genetic Vectors
  • Graft Rejection / prevention & control
  • Histocompatibility Antigens Class I / genetics*
  • Humans
  • Killer Cells, Natural / immunology
  • Lentivirus / genetics
  • Monocytes / immunology
  • RNA Interference*
  • Stem Cell Transplantation / methods*

Substances

  • Histocompatibility Antigens Class I
  • Complement System Proteins