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

Proc Natl Acad Sci U S A. 1989 Dec;86(23):9514-8. doi: 10.1073/pnas.86.23.9514.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Line
  • Cell Transformation, Viral
  • Cells, Cultured
  • Cytotoxicity, Immunologic*
  • Gene Expression
  • Genes, Viral
  • HIV Seropositivity / immunology
  • HIV-1 / enzymology
  • HIV-1 / genetics
  • HIV-1 / immunology*
  • Herpesvirus 4, Human / genetics
  • Humans
  • RNA-Directed DNA Polymerase / genetics
  • T-Lymphocytes, Cytotoxic / cytology
  • T-Lymphocytes, Cytotoxic / immunology*
  • Vaccinia virus / genetics
  • Viral Structural Proteins / genetics

Substances

  • Viral Structural Proteins
  • RNA-Directed DNA Polymerase