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Blood, 30 April 2009, Vol. 113, No. 18, pp. 4250-4261. Prepublished online as a Blood First Edition Paper on January 23, 2009; DOI 10.1182/blood-2008-09-177741.
Submitted September 8, 2008
Division of Microbiology, Tulane National Primate Research Center, Covington, LA, United States * Corresponding author; email: capetrei{at}tulane.edu.
We investigated the impact of rhesus macaque (RM) B cell depletion prior to inoculation with the isolate SIVsmmD215. Seven RMs were treated every three weeks with 50 mg/kg of an anti-CD20 antibody (Rituxan) starting seven days prior to inoculation for two months (n=4) and five months (n=3), respectively. Four control animals received no antibody. Three animals were completely depleted of CD20+ B cells, but four were only partially depleted of CD20 cells in the LNs and intestine. The decrease in antibody production was consistent with the efficacy of tissue CD20 depletion. Seroconversion and neutralizing antibody production was significantly delayed in animals showing complete tissue CD20 depletion and remained at low titers in all CD20-depleted RMs. Surprisingly, there was no significant difference in acute or chronic viral loads between CD20-depleted and control animal groups. There was a tendency for lower viral set-points in CD20-depleted animals. At 6 weeks post-inoculation, cellular immune responses were significantly stronger in CD20-depleted animals than in controls. There was no significant difference in survival between CD20-depleted and control animals. Our data suggest that a deficiency of Ab responses did not markedly affect viral replication or disease progression and that they may be compensated by more robust cellular responses.
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