Cytotoxic T lymphocytes (CTL) play an important role in the control of huma
n immunodeficiency virus (HIV) infection. CTL responses have been demonstra
ted for most of the HIV gene products, predominantly gag, pal, and env-enco
ded proteins, and also for the regulatory proteins Nef, Tat, Vif, or Rev. T
he HIV-1 reverse transcriptase (RT), which derives from expression of the p
ol gene, is an important target of cellular immune responses in infected in
dividuals. More than 40 different peptides containing RT-specific CTL epito
pes have been identified. The most conserved and frequently detected are lo
cated in the 'fingers' and 'palm' subdomains of the enzyme, but other epito
pes have been found in the 'thumb' and 'connection' subdomains as well as i
n the RNase Ii domain. Studies on the sequence variability and functional r
ole of amino acids forming CTL epitopes are relevant for addressing importa
nt questions relative to viral escape from immune control and the future de
sign of anti-AIDS vaccines.