Abacavir induced T cell reactivity from drug naïve individuals shares features of allo-immune responses

PLoS One. 2014 Apr 21;9(4):e95339. doi: 10.1371/journal.pone.0095339. eCollection 2014.

Abstract

Abacavir hypersensitivity is a severe hypersensitivity reaction which occurs exclusively in carriers of the HLA-B*57∶01 allele. In vitro culture of PBMC with abacavir results in the outgrowth of abacavir-reacting CD8+ T cells, which release IFNγ and are cytotoxic. How this immune response is induced and what is recognized by these T cells is still a matter of debate. We analyzed the conditions required to develop an abacavir-dependent T cell response in vitro. The abacavir reactivity was independent of co-stimulatory signals, as neither DC maturation nor release of inflammatory cytokines were observed upon abacavir exposure. Abacavir induced T cells arose in the absence of professional APC and stemmed from naïve and memory compartments. These features are reminiscent of allo-reactivity. Screening for allo-reactivity revealed that about 5% of generated T cell clones (n = 136) from three donors were allo-reactive exclusively to the related HLA-B*58∶01. The addition of peptides which can bind to the HLA-B*57∶01-abacavir complex and to HLA-B*58∶01 during the induction phase increased the proportion of HLA-B*58∶01 allo-reactive T cell clones from 5% to 42%. In conclusion, abacavir can alter the HLA-B*57∶01-peptide complex in a way that mimics an allo-allele ('altered self-allele') and create the potential for robust T cell responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD8-Positive T-Lymphocytes / drug effects*
  • CD8-Positive T-Lymphocytes / immunology*
  • Cell Compartmentation / drug effects
  • Clone Cells
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Dideoxynucleosides / pharmacology*
  • HLA-B Antigens / immunology
  • Histocompatibility Testing
  • Humans
  • Immunity, Innate / drug effects*
  • Immunologic Memory / drug effects
  • Lymphocyte Activation / drug effects
  • Models, Molecular
  • Peptides / chemistry
  • Peptides / immunology
  • Receptors, Antigen, T-Cell / metabolism
  • Tissue Donors

Substances

  • Dideoxynucleosides
  • HLA-B Antigens
  • Peptides
  • Receptors, Antigen, T-Cell
  • abacavir

Grants and funding

This work was supported by the Swiss National Science Foundation (SNF grant Nr. 310030-129828-1) and by the Swiss Center for Applied Human Toxicology (SCAHT). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.