Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2138335 | Leukemia Research | 2009 | 14 Pages |
Abstract
The breaking of peripheral T-cell tolerance toward self-antigens expressed by tumor cells and the subsequent establishment of an effective tumor protective immune response remains a major challenge for cancer immunotherapy. We report that both protective and therapeutic anti-tumor immune responses can be achieved in a mouse leukemia/lymphoma tumor model through the strong adjuvant effects provided by allogeneic CD3/CD28 cross-linked Th1 memory cells. The adjuvant effect of these cells is mediated by their ability to produce a variety of ‘danger signals’ which serve to deviate native non-protective Th2 anti-leukemia immune responses to effective Th1 immune responses.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Cancer Research
Authors
M. Har-Noy, M. Zeira, L. Weiss, E. Fingerut, R. Or, S. Slavin,