A new mechanism for IL-5-dependent helminth control: Neutrophil accumulation and neutrophil-mediated worm encapsulation in murine filariasis are abolished in the absence of IL-5

Khaled M. Al-Qaoud, Eric Pearlman, Thomas Hartung, Jan Klukowski, Bernhard Fleischer, Achim Hoerauf

Research output: Contribution to journalArticle

Abstract

IL-5 production and eosinophilia are features of helminth infections, but results concerning the role of IL-5 and eosinophils (EP) in worm control are contradictory. We describe here a novel, IL-5-dependent mechanism of helminth control in vivo, using a fully permissive murine filariasis model, i.e. infection of BALB/c mice with Litomosoides sigmodontis. Worm control was exerted by the formation of inflammatory nodules around adult filariae which initially remained alive but were eventually killed within several weeks. The cell population essential for inflammatory nodule formation was found to be neutrophils (NP) but not EP. Neutralization of IL-5 led to a failure of both EP and NP accumulation at the site of infection (i.e. the thoracic cavity), resulting in cessation of inflammatory nodule formation around worms and in their survival. The role of NP in this process was confirmed by treatment of mice with anti-granulocyte colony stimulating factor (G-CSF) which also resulted in a lack of inflammatory nodule formation and worm killing albeit in the presence of EP. Since IL-5, due to the absence of IL-5 receptors on NP, does not act on these cells directly, it was investigated if anti-IL-5 altered the production of NP-chemotactic cytokines. In anti-IL-5-treated mice, cytokines known to promote NP accumulation like tumor necrosis factor-α, G-CSF and KC (IL-8) were found to be strongly reduced, while NP-deactivating cytokines like IL-10 were increased. In conclusion, IL-5 constitutes a cytokine essential for NP-mediated worm control in filarial infection.

Original languageEnglish (US)
Pages (from-to)899-908
Number of pages10
JournalInternational Immunology
Volume12
Issue number6
StatePublished - 2000
Externally publishedYes

Fingerprint

Filariasis
Helminths
Interleukin-5
Neutrophils
Eosinophils
Granulocyte Colony-Stimulating Factor
Cytokines
Infection
Interleukin-5 Receptors
Filarioidea
Thoracic Cavity
Eosinophilia
Interleukin-8
Chemokines
Interleukin-10
Tumor Necrosis Factor-alpha

Keywords

  • Animal model
  • Cytokines
  • Eosinophils
  • Helminth infection
  • Neutrophils

ASJC Scopus subject areas

  • Immunology

Cite this

A new mechanism for IL-5-dependent helminth control : Neutrophil accumulation and neutrophil-mediated worm encapsulation in murine filariasis are abolished in the absence of IL-5. / Al-Qaoud, Khaled M.; Pearlman, Eric; Hartung, Thomas; Klukowski, Jan; Fleischer, Bernhard; Hoerauf, Achim.

In: International Immunology, Vol. 12, No. 6, 2000, p. 899-908.

Research output: Contribution to journalArticle

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abstract = "IL-5 production and eosinophilia are features of helminth infections, but results concerning the role of IL-5 and eosinophils (EP) in worm control are contradictory. We describe here a novel, IL-5-dependent mechanism of helminth control in vivo, using a fully permissive murine filariasis model, i.e. infection of BALB/c mice with Litomosoides sigmodontis. Worm control was exerted by the formation of inflammatory nodules around adult filariae which initially remained alive but were eventually killed within several weeks. The cell population essential for inflammatory nodule formation was found to be neutrophils (NP) but not EP. Neutralization of IL-5 led to a failure of both EP and NP accumulation at the site of infection (i.e. the thoracic cavity), resulting in cessation of inflammatory nodule formation around worms and in their survival. The role of NP in this process was confirmed by treatment of mice with anti-granulocyte colony stimulating factor (G-CSF) which also resulted in a lack of inflammatory nodule formation and worm killing albeit in the presence of EP. Since IL-5, due to the absence of IL-5 receptors on NP, does not act on these cells directly, it was investigated if anti-IL-5 altered the production of NP-chemotactic cytokines. In anti-IL-5-treated mice, cytokines known to promote NP accumulation like tumor necrosis factor-α, G-CSF and KC (IL-8) were found to be strongly reduced, while NP-deactivating cytokines like IL-10 were increased. In conclusion, IL-5 constitutes a cytokine essential for NP-mediated worm control in filarial infection.",
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AU - Pearlman, Eric

AU - Hartung, Thomas

AU - Klukowski, Jan

AU - Fleischer, Bernhard

AU - Hoerauf, Achim

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