4.6 Article

Emergence and kinetics of simian immunodeficiency virus-specific CD8+ T cells in the intestines of macaques during primary infection

Journal

JOURNAL OF VIROLOGY
Volume 75, Issue 21, Pages 10515-10519

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.75.21.10515-10519.2001

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Funding

  1. NCI NIH HHS [N01-CO-56000] Funding Source: Medline
  2. NCRR NIH HHS [P51 RR000168, K26 RR000168, RR00168] Funding Source: Medline
  3. NIAID NIH HHS [AI45314, R01 AI049080, AI49080] Funding Source: Medline
  4. NICHD NIH HHS [HD36310] Funding Source: Medline
  5. NIDDK NIH HHS [R01 DK050550, DK50550] Funding Source: Medline

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In this report, three Mamu-A*01(+) rhesus macaques were examined to compare the emergence of simian immunodeficiency virus (SIV)-specific CD8(+) T cells in the intestines and blood in early SIV infection using a major histocompatibility complex class I tetramer complexed with the Gag(181-189) peptide. Fourteen days after intravenous inoculation with SIVmac251, large numbers of SrV Gag(181-189)-specific CD8(+) T cells were detected in the intestinal mucosa (3.1 to 11.5% of CD3(+) CD8(+) lymphocytes) as well as in the blood (3.1 to 13.4%) of all three macaques. By 21 days postinoculation, levels of tetramer-binding cells had dropped in both the intestines and blood. At day 63, however, levels of SIV Gag(181-189)- specific CD8(+) T cells in the intestines had rebounded in all three macaques to levels that were higher (8.6 to 18.7%) than those at day 21. In contrast, percentages of tetramer-binding cells in the peripheral blood remained comparatively stable (2.5 to 4.5%) at this time point. In summary, SFV Gag(181-189)-specific CD8(+) T cells appeared in both the intestinal mucosa and peripheral blood at a comparable rate and magnitude in primary SIV infection. Given that the intestine is a major site of early viral replication as well as the site where most of the total body lymphocyte pool resides, these data indicate that it is also an early and important site of development of antiviral immune responses.

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