Skip to main content
eScholarship
Open Access Publications from the University of California

Genetic and stochastic influences on the interaction of human immunodeficiency virus type 1 and cytotoxic T lymphocytes in identical twins

  • Author(s): Yang, Otto O
  • Church, Joseph
  • Kitchen, Christina M R
  • Kilpatrick, Ryan
  • Ali, Ayub
  • Geng, Yongzhi
  • Killian, M Scott
  • Sabado, Rachel Lubong
  • Ng, Hwee
  • Suen, Jeffrey
  • Bryson, Yvonne
  • Jamieson, Beth D
  • Krogstad, Paul
  • et al.
Abstract

Human immunodeficiency virus type 1 (HIV-1) evolves in vivo under selective pressure from CD8(+) T-lymphocyte (CTL) responses, which are in turn determined by host and viral genetic factors, such as restricting major histocompatibility complex molecules and the available viral epitope sequences. However, CTL are derived stochastically through the random gene rearrangements to produce T-cell receptors (TCR), and the relative impact of genetic versus stochastic processes on CTL targeting of HIV and immune-driven viral evolution is unclear. Here we evaluate identical twins infected with HIV-1 as neonates from a common blood transfusion, with subsequently similar environmental exposures, thereby allowing controlled comparisons of CTL targeting and viral evolution. Seventeen years after infection, their CTL targeting of HIV-1 was remarkably similar. In contrast, their overall TCR profiles were highly dissimilar, and a dominant epitope was recognized by distinctly different TCR in each twin. Furthermore, their viral epitopes had diverged, and there was ongoing viral phylogenetic divergence between the twins between 12 and 17 years after infection. These results indicate that while CTL targeting is predominately genetically determined, stochastic influences render the interaction of HIV-1 and host immunity, and therefore viral escape and CTL efficacy, unpredictable.

Many UC-authored scholarly publications are freely available on this site because of the UC Academic Senate's Open Access Policy. Let us know how this access is important for you.

Main Content
Current View