Frontiers in Immunology (Mar 2019)

A Pathogenic Role for Splenic B1 Cells in SIV Disease Progression in Rhesus Macaques

  • Gospel Enyindah-Asonye,
  • Anthony Nwankwo,
  • Christopher Hogge,
  • Mohammad Arif Rahman,
  • Sabrina Helmold Hait,
  • Ruth Hunegnaw,
  • Eun-Ju Ko,
  • Tanya Hoang,
  • David J. Venzon,
  • Marjorie Robert-Guroff

DOI
https://doi.org/10.3389/fimmu.2019.00511
Journal volume & issue
Vol. 10

Abstract

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B1 cells spontaneously produce protective natural antibodies which provide the first line of defense against a variety of pathogens. Although these natural antibodies share similar autoreactive features with several HIV-1 broadly neutralizing antibodies, the role of B1 cells in HIV/SIV disease progression is unknown. We report the presence of human-like B1 cells in rhesus macaques. During chronic SIV infection, we found that the frequency of splenic CD11b+ B1 cells positively correlated with plasma SIV viral load and exhausted T cells. Mechanistically, we discovered that splenic CD11b+ B1 cells express PD-L2 and IL-10, and were able to induce PD-1 upregulation on CD4+ T cells in vitro. These findings suggest that splenic CD11b+ B1 cells may contribute to the regulation of SIV plasma viral load by enhancing T cell exhaustion. Therefore, understanding the mechanisms that govern their function in rhesus macaques may lead to novel therapeutic strategies for impeding HIV/SIV disease progression.

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