Advances in our understanding of the role of cytotoxic T lymphocytes (CTLs)
in the control of Epstein-Barr virus (EBV)-associated malignancies and the
overall biology of these diseases have led to the development of novel the
rapeutic strategies designed to specifically target viral antigens expresse
d in these malignancies. Long-term success of many of these strategies is c
onstrained by the latency phenotypes adopted by different diseases. Adoptiv
e transfer of polyclonal virus-specific CTLs has been used successfully to
reverse the outgrowth of malignancies such as post-transplant lymphoprolife
rative disease (PTLD). On the other hand, limited viral gene expression in
other EBV-associated malignancies such as Burkitt's lymphoma, Hodgkin's dis
ease and nasopharyngeal carcinoma limits the efficacy of immunotherapeutic
strategies used for PTLD. Preclinical studies based on specific targeting o
f viral antigens expressed in these malignancies have provided very encoura
ging results and thus are likely to serve as an important platform for the
treatment of human patients.