Long-term culture and fine specificity of human cytotoxic T-lymphocyte clones reactive with human immunodeficiency virus type 1.

BD Walker, C Flexner… - Proceedings of the …, 1989 - National Acad Sciences
BD Walker, C Flexner, K Birch-Limberger, L Fisher, TJ Paradis, A Aldovini, R Young, B Moss
Proceedings of the National Academy of Sciences, 1989National Acad Sciences
The definition of human immunodeficiency virus type 1 (HIV-1) immunogenic epitopes is
central to the rational design of AIDS vaccine strategies. In this study, we have generated
seven HIV-1 reverse transcriptase-specific cytotoxic T-lymphocyte (CTL) clones from the
peripheral blood of two seropositive subjects. Epitopes recognized by these CTL clones
were identified by using target cells infected with recombinant HIV-1-vaccinia virus vectors
expressing truncated reverse transcriptase proteins and further defined by using target cells …
The definition of human immunodeficiency virus type 1 (HIV-1) immunogenic epitopes is central to the rational design of AIDS vaccine strategies. In this study, we have generated seven HIV-1 reverse transcriptase-specific cytotoxic T-lymphocyte (CTL) clones from the peripheral blood of two seropositive subjects. Epitopes recognized by these CTL clones were identified by using target cells infected with recombinant HIV-1-vaccinia virus vectors expressing truncated reverse transcriptase proteins and further defined by using target cells incubated with overlapping 25-amino acid synthetic reverse transcriptase peptides. Five different CTL epitopes were identified, and in each case recognition was restricted by class I human leukocyte antigens (HLA). Clones maintained specific cytolytic function in continuous culture for up to 11 months, requiring only periodic restimulation with a CD3-specific monoclonal antibody. These results indicate that HIV-1-specific, major histocompatibility class I-restricted CTL recognize multiple epitopes of a single viral gene product in conjunction with different host HLA antigens. In addition, they demonstrate that human virus-specific CTL can be grown in long-term culture without the need for reexposure to viral antigen.
National Acad Sciences