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Functional cure of SIVagm infection in rhesus macaques results in complete recovery of CD4+ T cells and is reverted by CD8+ cell depletion.

Publication ,  Journal Article
Pandrea, I; Gaufin, T; Gautam, R; Kristoff, J; Mandell, D; Montefiori, D; Keele, BF; Ribeiro, RM; Veazey, RS; Apetrei, C
Published in: PLoS Pathog
August 2011

Understanding the mechanism of infection control in elite controllers (EC) may shed light on the correlates of control of disease progression in HIV infection. However, limitations have prevented a clear understanding of the mechanisms of elite controlled infection, as these studies can only be performed at randomly selected late time points in infection, after control is achieved, and the access to tissues is limited. We report that SIVagm infection is elite-controlled in rhesus macaques (RMs) and therefore can be used as an animal model for EC HIV infection. A robust acute infection, with high levels of viral replication and dramatic mucosal CD4(+) T cell depletion, similar to pathogenic HIV-1/SIV infections of humans and RMs, was followed by complete and durable control of SIVagm replication, defined as: undetectable VLs in blood and tissues beginning 72 to 90 days postinoculation (pi) and continuing at least 4 years; seroreversion; progressive recovery of mucosal CD4(+) T cells, with complete recovery by 4 years pi; normal levels of T cell immune activation, proliferation, and apoptosis; and no disease progression. This "functional cure" of SIVagm infection in RMs could be reverted after 4 years of control of infection by depleting CD8 cells, which resulted in transient rebounds of VLs, thus suggesting that control may be at least in part immune mediated. Viral control was independent of MHC, partial APOBEC restriction was not involved in SIVagm control in RMs and Trim5 genotypes did not impact viral replication. This new animal model of EC lentiviral infection, in which complete control can be predicted in all cases, permits research on the early events of infection in blood and tissues, before the defining characteristics of EC are evident and when host factors are actively driving the infection towards the EC status.

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Published In

PLoS Pathog

DOI

EISSN

1553-7374

Publication Date

August 2011

Volume

7

Issue

8

Start / End Page

e1002170

Location

United States

Related Subject Headings

  • Virus Replication
  • Virology
  • Time Factors
  • Simian immunodeficiency virus
  • Simian Immunodeficiency Virus
  • Simian Acquired Immunodeficiency Syndrome
  • Macaca mulatta
  • Lymphocyte Activation
  • Humans
  • CD8-Positive T-Lymphocytes
 

Citation

APA
Chicago
ICMJE
MLA
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Pandrea, I., Gaufin, T., Gautam, R., Kristoff, J., Mandell, D., Montefiori, D., … Apetrei, C. (2011). Functional cure of SIVagm infection in rhesus macaques results in complete recovery of CD4+ T cells and is reverted by CD8+ cell depletion. PLoS Pathog, 7(8), e1002170. https://doi.org/10.1371/journal.ppat.1002170
Pandrea, Ivona, Thaidra Gaufin, Rajeev Gautam, Jan Kristoff, Daniel Mandell, David Montefiori, Brandon F. Keele, Ruy M. Ribeiro, Ronald S. Veazey, and Cristian Apetrei. “Functional cure of SIVagm infection in rhesus macaques results in complete recovery of CD4+ T cells and is reverted by CD8+ cell depletion.PLoS Pathog 7, no. 8 (August 2011): e1002170. https://doi.org/10.1371/journal.ppat.1002170.
Pandrea I, Gaufin T, Gautam R, Kristoff J, Mandell D, Montefiori D, et al. Functional cure of SIVagm infection in rhesus macaques results in complete recovery of CD4+ T cells and is reverted by CD8+ cell depletion. PLoS Pathog. 2011 Aug;7(8):e1002170.
Pandrea, Ivona, et al. “Functional cure of SIVagm infection in rhesus macaques results in complete recovery of CD4+ T cells and is reverted by CD8+ cell depletion.PLoS Pathog, vol. 7, no. 8, Aug. 2011, p. e1002170. Pubmed, doi:10.1371/journal.ppat.1002170.
Pandrea I, Gaufin T, Gautam R, Kristoff J, Mandell D, Montefiori D, Keele BF, Ribeiro RM, Veazey RS, Apetrei C. Functional cure of SIVagm infection in rhesus macaques results in complete recovery of CD4+ T cells and is reverted by CD8+ cell depletion. PLoS Pathog. 2011 Aug;7(8):e1002170.

Published In

PLoS Pathog

DOI

EISSN

1553-7374

Publication Date

August 2011

Volume

7

Issue

8

Start / End Page

e1002170

Location

United States

Related Subject Headings

  • Virus Replication
  • Virology
  • Time Factors
  • Simian immunodeficiency virus
  • Simian Immunodeficiency Virus
  • Simian Acquired Immunodeficiency Syndrome
  • Macaca mulatta
  • Lymphocyte Activation
  • Humans
  • CD8-Positive T-Lymphocytes