Dysfunctional HIV-specific CD8+ T cell proliferation is associated with increased caspase-8 activity and mediated by necroptosis

Gaurav D. Gaiha, Kevin J. McKim, Matthew Woods, Thomas Pertel, Janine Rohrbach, Natasha Barteneva, Christopher R. Chin, Dongfang Liu, Damien Z. Soghoian, Kevin Cesa, Shannon Wilton, Michael T. Waring, Adam Chicoine, Travis Doering, E. John Wherry, Daniel E. Kaufmann, Mathias Lichterfeld, Abraham L. Brass, Bruce D. Walker

Research output: Contribution to journalArticle

34 Scopus citations

Abstract

Decreased HIV-specific CD8+ Tcell proliferation is a hallmark of chronic infection, but the mechanisms of decline are unclear. We analyzed gene expression profiles from antigen-stimulated HIV-specific CD8+ Tcells from patients with controlled and uncontrolled infection and identified caspase-8 as a correlate of dysfunctional CD8+ Tcell proliferation. Caspase-8 activity was upregulated in HIV-specific CD8+ Tcells from progressors and correlated positively with disease progression and programmed cell death-1 (PD-1) expression, but negatively with proliferation. In addition, progressor cells displayed a decreased ability to upregulate membrane-associated caspase-8 activity and increased necrotic cell death following antigenic stimulation, implicating the programmed cell death pathway necroptosis. Invitro necroptosis blockade rescued HIV-specific CD8+ Tcell proliferation in progressors, as did silencing of necroptosis mediator RIPK3. Thus, chronic stimulation leading to upregulated caspase-8 activity contributes to dysfunctional HIV-specific CD8+ Tcell proliferation through activation of necroptosis and increased cell death.

Original languageEnglish (US)
Pages (from-to)1001-1012
Number of pages12
JournalImmunity
Volume41
Issue number6
DOIs
StatePublished - Dec 18 2014

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Infectious Diseases

Fingerprint Dive into the research topics of 'Dysfunctional HIV-specific CD8<sup>+</sup> T cell proliferation is associated with increased caspase-8 activity and mediated by necroptosis'. Together they form a unique fingerprint.

Cite this