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Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel
The MHC class I-restricted CD8 CTL effector arm of the adaptive
immune response is uniquely equipped to recognize tumor cells as
foreign and consequently initiates the cascade of events resulting in
their destruction. However, tumors have developed sophisticated
strategies to escape immune effector mechanisms; their most well-known
strategy is down-regulation of MHC class I molecules. To overcome this
and develop new approaches for immunotherapy, we have constructed a
recombinant molecule in which a single-chain MHC is specifically
targeted to tumor cells through its fusion to cancer-specific
recombinant Ab fragments. As a model we used a single-chain HLA-A2
molecule genetically fused to the variable domains of an
anti-IL-2R
subunit-specific humanized Ab, anti-Tac. The
construct, termed B2M-aTac(dsFv), was expressed in
Escherichia coli, and functional molecules were produced
by in vitro refolding in the presence of HLA-A2-restricted antigenic
peptides. Flow cytometry studies revealed the ability to decorate
Ag-positive, HLA-A2-negative human tumor cells with HLA-A2-peptide
complexes in a manner that was entirely dependent upon the specificity
of the targeting Ab fragment. Most importantly, the
B2M-aTac(dsFv)-mediated coating of the target tumor cells made them
susceptible for efficient and specific HLA-A2-restricted, melanoma
gp100 peptide-specific CTL-mediated lysis. These results demonstrate
the concept that Ab-guided, Ag-specific targeting of MHC-peptide
complexes on tumor cells can render them susceptible and more receptive
and thus potentiate CTL killing. This type of approach may open the way
for the development of new immunotherapeutic strategies based on Ab
targeting of natural cognate MHC ligands and CTL-based cytotoxic
mechanisms.
This article has been cited by other articles:
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C. Germain, C. Larbouret, V. Cesson, A. Donda, W. Held, J.-P. Mach, A. Pelegrin, and B. Robert MHC Class I-Related Chain A Conjugated to Antitumor Antibodies Can Sensitize Tumor Cells to Specific Lysis by Natural Killer Cells Clin. Cancer Res., October 15, 2005; 11(20): 7516 - 7522. [Abstract] [Full Text] [PDF] |
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