Impact of filarial infections on coincident intracellular pathogens: Mycobacterium tuberculosis and Plasmodium falciparum

Curr Opin HIV AIDS. 2012 May;7(3):231-8. doi: 10.1097/COH.0b013e3283522c3d.

Abstract

Purpose of review: To examine the consequences of the immune modulation seen in chronic filarial infection on responses to intracellular pathogens (and their antigens) that are often co-endemic with filarial infections, namely Plasmodium and Mycobacterium tuberculosis.

Recent findings: Much of the recent data on filaria/mycobacteria or filaria/Plasmodium co-infection has focused on the modulation of mycobacteria-specific or malaria-specific responses by chronic filarial infection. As such, filarial infections very clearly alter the magnitude and quality of the mycobacteria-specific or malaria-specific cytokine responses, responses that have been typically associated with control of these intracellular pathogens.

Summary: Although phylogenetically distinct, mycobacteria and Plasmodium spp. often share the same geographical niche with filarial infections. The complex interplay between filarial parasites that are associated with immunomodulation and those microbial pathogens that require a proinflammatory or unmodulated response for their control is easily demonstrable ex vivo, but whether this interplay affects disease outcome in tuberculosis or malaria remains an open question.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • Coinfection / immunology*
  • Coinfection / microbiology
  • Coinfection / parasitology
  • Cytokines
  • Filariasis / complications*
  • Filariasis / parasitology
  • Filarioidea / immunology*
  • Humans
  • Malaria, Falciparum / complications
  • Malaria, Falciparum / immunology*
  • Mycobacterium tuberculosis / immunology
  • Plasmodium falciparum / immunology
  • Tuberculosis / complications
  • Tuberculosis / immunology*

Substances

  • Cytokines