Consequences of cytotoxic T-lymphocyte escape

Common escape mutations in simian immunodeficiency virus are poorly recognized in naïve hosts

Thomas C. Friedrich, Adrian B. McDermott, Matthew R. Reynolds, Shari Piaskowski, Sarah Fuenger, Ivna P. De Souza, Richard Rudersdorf, Candice Cullen, Levi J. Yant, Lara Vojnov, Jason Stephany, Sarah Martin, David H. O'Connor, Nancy Wilson, David Watkins

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

Cytotoxic T lymphocytes (CTL) are associated with control of immunodeficiency virus infection but also select for variants that escape immune recognition. Declining frequencies of epitope-specific CTL frequencies have been correlated with viral escape in individual hosts. However, escape mutations may give rise to new epitopes that could be recognized by CTL expressing appropriate T-cell receptors and thus still be immunogenic when escape variants are passed to individuals expressing the appropriate major histocompatibility complex class I molecules. To determine whether peptide ligands that have been altered through escape can be immunogenic in new hosts, we challenged naïve, immunocompetent macaques with a molecularly cloned simian immunodeficiency virus (SIV) bearing common escape mutations in three immunodominant CTL epitopes. Responses to the altered peptides were barely detectable in fresh samples at any time after infection. Surprisingly, CTL specific for two of three escaped epitopes could be expanded by in vitro stimulation with synthetic peptides. Our results suggest that some escape variant epitopes evolving in infected individuals do not efficiently stimulate new populations of CTL, either in that individual or upon passage to new hosts. Nevertheless, escape variation may not completely abolish an epitope's immunogenicity. Moreover, since the mutant epitope sequences did not revert to wild type during the study period, it is possible that low-frequency CTL exerted enough selective pressure to preserve epitope mutations in viruses replicating in vivo.

Original languageEnglish
Pages (from-to)10064-10073
Number of pages10
JournalJournal of Virology
Volume78
Issue number18
DOIs
StatePublished - Sep 1 2004
Externally publishedYes

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Simian immunodeficiency virus
Simian Immunodeficiency Virus
cytotoxic T-lymphocytes
Cytotoxic T-Lymphocytes
epitopes
Epitopes
mutation
Mutation
Peptides
peptides
T-Lymphocyte Epitopes
viruses
Macaca
Virus Diseases
T-Cell Antigen Receptor
Major Histocompatibility Complex
synthetic peptides
immunosuppression
major histocompatibility complex
infection

ASJC Scopus subject areas

  • Immunology

Cite this

Consequences of cytotoxic T-lymphocyte escape : Common escape mutations in simian immunodeficiency virus are poorly recognized in naïve hosts. / Friedrich, Thomas C.; McDermott, Adrian B.; Reynolds, Matthew R.; Piaskowski, Shari; Fuenger, Sarah; De Souza, Ivna P.; Rudersdorf, Richard; Cullen, Candice; Yant, Levi J.; Vojnov, Lara; Stephany, Jason; Martin, Sarah; O'Connor, David H.; Wilson, Nancy; Watkins, David.

In: Journal of Virology, Vol. 78, No. 18, 01.09.2004, p. 10064-10073.

Research output: Contribution to journalArticle

Friedrich, TC, McDermott, AB, Reynolds, MR, Piaskowski, S, Fuenger, S, De Souza, IP, Rudersdorf, R, Cullen, C, Yant, LJ, Vojnov, L, Stephany, J, Martin, S, O'Connor, DH, Wilson, N & Watkins, D 2004, 'Consequences of cytotoxic T-lymphocyte escape: Common escape mutations in simian immunodeficiency virus are poorly recognized in naïve hosts', Journal of Virology, vol. 78, no. 18, pp. 10064-10073. https://doi.org/10.1128/JVI.78.18.10064-10073.2004
Friedrich, Thomas C. ; McDermott, Adrian B. ; Reynolds, Matthew R. ; Piaskowski, Shari ; Fuenger, Sarah ; De Souza, Ivna P. ; Rudersdorf, Richard ; Cullen, Candice ; Yant, Levi J. ; Vojnov, Lara ; Stephany, Jason ; Martin, Sarah ; O'Connor, David H. ; Wilson, Nancy ; Watkins, David. / Consequences of cytotoxic T-lymphocyte escape : Common escape mutations in simian immunodeficiency virus are poorly recognized in naïve hosts. In: Journal of Virology. 2004 ; Vol. 78, No. 18. pp. 10064-10073.
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