Blocking of α4β7 gut-homing integrin during acute infection leads to decreased plasma and gastrointestinal tissue viral loads in simian immunodeficiency virus-infected rhesus macaques.

نویسندگان

  • Aftab A Ansari
  • Keith A Reimann
  • Ann E Mayne
  • Yoshiaki Takahashi
  • Susan T Stephenson
  • Rijian Wang
  • Xinyue Wang
  • Jichu Li
  • Andrew A Price
  • Dawn M Little
  • Mohammad Zaidi
  • Robert Lyles
  • Francois Villinger
چکیده

Intravenous administration of a novel recombinant rhesus mAb against the α4β7 gut-homing integrin (mAb) into rhesus macaques just prior to and during acute SIV infection resulted in significant decrease in plasma and gastrointestinal (GI) tissue viral load and a marked reduction in GI tissue proviral DNA load as compared with control SIV-infected rhesus macaques. This mAb administration was associated with increases in peripheral blood naive and central memory CD4(+) T cells and maintenance of a high frequency of CCR5(+)CD4(+) T cells. Additionally, such mAb administration inhibited the mobilization of NK cells and plasmacytoid dendritic cells characteristically seen in the control animals during acute infection accompanied by the inhibition of the synthesis of MIP-3α by the gut tissues. These data in concert suggest that blocking of GI trafficking CD4(+) T cells and inhibiting the mobilization of cell lineages of the innate immune system may be a powerful new tool to protect GI tissues and modulate acute lentiviral infection.

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عنوان ژورنال:
  • Journal of immunology

دوره 186 2  شماره 

صفحات  -

تاریخ انتشار 2011