Identification of an interleukin (IL)-25–dependent cell population that provides IL-4, IL-5, and IL-13 at the onset of helminth expulsion

By P. Fallon, S. Ballantyne, Niamh E. Mangan, J. Barlow, A. Dasvarma, D. Hewett, Ann Mcilgorm, H. Jolin, Andrew N. J. McKenzie. Journal of Experimental Medicine, 2006

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Type 2 immunity, which involves coordinated regulation of innate and adaptive immune responses, can protect against helminth parasite infection, but may lead to allergy and asthma after inappropriate activation. We demonstrate that il25−/− mice display inefficient Nippostrongylus brasiliensis expulsion and delayed cytokine production by T helper 2 cells. We further establish a key role for interleukin (IL)-25 in regulating a novel population of IL-4–, IL-5–, IL-13–producing non–B/non–T (NBNT), c-kit+, FcɛR1− cells during helminth infection. A deficit in this population in il25−/− mice correlates with inefficient N. brasiliensis expulsion. In contrast, administration of recombinant IL-25 in vivo induces the appearance of NBNT, c-kit+, FcɛR1− cells and leads to rapid worm expulsion that is T and B cell independent, but type 2 cytokine dependent. We demonstrate that these IL-25–regulated cells appear rapidly in the draining lymph nodes, implicating them as a source of type 2 cytokines during initiation of worm expulsion.

Subfields: Immunology, Parasitology, Small Animals

View Paper: https://www.semanticscholar.org/paper/8448eb332ed530e44ddfa7d094673de767e65612

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In Immunology

  1. R. Locksley
  2. H. Hammad
  3. S. Gordon
  4. F. Martínez
  5. B. Lambrecht
  6. Jinfang Zhu
  7. W. E. Paul
  8. H. Spits

In Parasitology

  1. R. Locksley
  2. A. Mantovani

In Small Animals

  1. R. Locksley

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