[HTML][HTML] Direct isolation, phenotyping and cloning of low-frequency antigen-specific cytotoxic T lymphocytes from peripheral blood

PR Dunbar, GS Ogg, J Chen, N Rust… - Current Biology, 1998 - cell.com
PR Dunbar, GS Ogg, J Chen, N Rust, P van der Bruggen, V Cerundolo
Current Biology, 1998cell.com
Cytotoxic T lymphocytes (CTLs) play an important role in controlling viral infections and
certain tumours, but characterising specific CTL responses has always been technically
limited. Fluorogenic 'tetramers' of major histocompatibility complex (MHC) class I complexes
have been exploited recently to quantify the massive expansion of specific CTLs in human
immunodeficiency virus (HIV) infection [1]. Here, we use MHC class I complex tetramers to
isolate low-frequency antigen-specific CTLs directly from human peripheral blood, allowing …
Abstract
Cytotoxic T lymphocytes (CTLs) play an important role in controlling viral infections and certain tumours, but characterising specific CTL responses has always been technically limited. Fluorogenic ‘tetramers' of major histocompatibility complex (MHC) class I complexes have been exploited recently to quantify the massive expansion of specific CTLs in human immunodeficiency virus (HIV) infection [1]. Here, we use MHC class I complex tetramers to isolate low-frequency antigen-specific CTLs directly from human peripheral blood, allowing the simultaneous phenotypic and functional characterisation and cloning of these CTLs. We synthesised a tetramer that specifically stained human leukocyte antigen (HLA)-A2.1-restricted CTL clones recognising the influenza matrix protein peptide 58–66, matrix 58–66 [2]. This tetramer stained between 1 in 1,500 and 1 in 58,000 peripheral blood mononuclear cells (PBMCs) from HLA-A2.1+ individuals. The surface phenotype of these cells could be analysed by fluorescence-activated cell sorting (FACS), and the cells could be directly sorted into enzyme-linked immunospot (ELISpot) plates, where they released interferon-γ (IFN-γ) within 1 day of antigen exposure. The same population was cloned by FACS, and the specificity of several expanded clones was confirmed. Cloning was greatly simplified and accelerated compared with standard protocols, and was highly efficient. We also used tetramer-based sorting to enrich melanoma-specific CTLs derived from a tumour-infiltrated lymph node. Direct cloning of specific CTLs from peripheral blood can provide important information about immunological memory, CTL responses against tumour antigens and CTL proliferation and function, and opens up new possibilities for generating CTLs for adoptive immunotherapy.
cell.com