Volume 10 Supplement 1

2nd Cross Company Respiratory Symposium

Open Access

Exploring the role of SYK in respiratory in vivo models

  • Michael Caniga1,
  • Janice D Woodhouse1,
  • Alan Wilhelm1,
  • Malgorzata A Gil1,
  • Yanlin Jia1,
  • Hongshi Yu1,
  • Stella Vincent1,
  • Richard Miller1,
  • Gissela Lieber2,
  • Xiomara Fernandez2,
  • Richard Chapman2,
  • Robbie McLeod1,
  • Lily Y Moy1,
  • Nancy Kelly1,
  • Emily Hickey2,
  • Michael A Crackower1,
  • Thomas Miller1,
  • William M Abraham3 and
  • Milenko Cicmil1
Journal of Inflammation201310(Suppl 1):P11

https://doi.org/10.1186/1476-9255-10-S1-P11

Published: 14 August 2013

Background

Spleen Tyrosine Kinase (SYK) is a key activator of signaling pathways downstream of multiple surface receptors implicated in asthma. SYK function has been extensively studied in Last cells downstream of the high-affinity IgE receptor (FcεR1). Most studies evaluating SYK function in preclinical models have relied on poorly selective compounds, anti-sense oligonucleotides, or SYK knockout mice. Here we describe the characterization of SYK mechanism in multiple in vivo model settings.

Materials and methods

The effect of SYK inhibitor MRK-A on allergic airway responses was evaluated in IgE-mediated tracheal extravasation in rat, Brown Norway Ova rat models of allergic inflammation and the sheep inhaled ascaris allergen challenge model.

Results

MRK-A dose-dependently blocked IgE-mediated tracheal extravasation in rat. In a Brown Norway rat ovalbumin-sensitized airway challenge model oral dosing of MRK-A led to a dose-dependent inhibition of airway inflammation. Intravenous dosing of MRK-A was able to significantly inhibit both early and late allergen- induced changes in airway resistance in an ascaris-sensitive sheep allergen challenge model as well as airway hyper responsiveness.

Conclusions

Here we demonstrated that SYK mechanism plays a significant role in several in vivo allergen challenge models. This ranges from simple PK/PD mast cells driven models such as the IgE-mediated tracheal extravasation to the more complex and clinically relevant sheep inhaled allergen challenge model.

Authors’ Affiliations

(1)
Merck Research Laboratories
(2)
Merck Research Laboratories
(3)
Mount Sinai Medical Center

Copyright

© Caniga et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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