The lectin pathway of complement: advantage or disadvantage in HIV pathogenesis?

Clin Immunol. 2014 Sep;154(1):13-25. doi: 10.1016/j.clim.2014.06.002. Epub 2014 Jun 11.

Abstract

The pattern recognition molecules of the lectin complement pathway are important components of the innate immune system with known functions in host-virus interactions. This paper summarizes current knowledge of how these intriguing molecules, including mannose-binding lectin (MBL), Ficolin-1, -2 and -3, and collectin-11 (CL-11) may influence HIV-pathogenesis. It has been demonstrated that MBL is capable of binding and neutralizing HIV and may affect host susceptibility to HIV infection and disease progression. In addition, MBL may cause variations in the host immune response against HIV. Ficolin-1, -2 and -3 and CL-11 could have similar functions in HIV infection as the ficolins have been shown to play a role in other viral infections, and CL-11 resembles MBL and the ficolins in structure and binding capacity.

Keywords: Collectin-11; Ficolin-1, -2 and -3; HIV; Innate immunity; Lectin pathway; Mannose-binding lectin (MBL).

Publication types

  • Review

MeSH terms

  • Complement Pathway, Mannose-Binding Lectin / genetics
  • Complement Pathway, Mannose-Binding Lectin / immunology*
  • HIV Infections / immunology*
  • HIV Infections / physiopathology
  • Humans
  • Models, Biological
  • Polymorphism, Genetic