4.6 Article

Induction of IL-22 protein and IL-22-producing cells in rainbow trout Oncorhynchus mykiss

Journal

DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
Volume 101, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dci.2019.103449

Keywords

Rainbow trout; Interleukin-22; Transcript expression; Protein expression; Monoclonal antibody

Funding

  1. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/N024052/1, BB/R008442/1]
  2. European Commission under the 7th Framework Programme for Research and Technological Development (FP7) of the European Union [311993 TARGETFISH]
  3. Ministry of Education, Republic of China (Taiwan)
  4. Ministry of Science and Technology, Republic of China (Taiwan) [MOST 107-2917-1-564-019]
  5. Newton International Fellowship - Academy of Medical Sciences, UK (AMS) [NIF004\1036]
  6. BBSRC [BB/N024052/1, BB/R008442/1] Funding Source: UKRI

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IL-22 is a critical cytokine which is involved in modulating tissue responses during inflammation, and is produced mainly by T cells and innate leucocytes. In mammals, IL-22 is a key component in mucosal defences, tissue repair, epithelial cell survival and proliferation. In teleosts, IL-22 has been cloned and studied in several species, and the transcript is highly expressd in mucosal tissues and induced by pathogen associated molecular patterns (PAMPs), suggesting IL-22 also functions as an important component of the innate immune response in fish. To investigate these immune responses further, we have validated and characterised two monoclonal antibodies (mAbs) which were raised against two different peptide immunogens of salmonid IL-22. Our results show that both mAbs specifically react to their own peptide immunogens and recombinant IL-22, and are able to detect the induction of native protein expression after stimulation. In flow cytometry, an increase in IL-22 positive cells was detected after stimulation in vitro with cytokines and PAMPs and in vivo after bacterial challenge. The immunohistochemistry results showed that IL-22 is highly upregulated in the gills after challenge, both in cells within the gill filaments and in the interbranchial lymphoid tissue. Such results suggest IL-22 may have a role in triggering local antimicrobial defences in fish that may facilitate efficient microbial clearance. Hence monitoring IL-22 producing cells/protein secretion may provide an alternative mean to assess the effectiveness of mucosal vaccines.

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