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Published on: June 13, 2013
Trypsin inhibitory capacity in vernal keratoconjunctivitis
Saeid Ghavami1, Mohammad Hashemi, Fredrick J de Serres
1Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Investigative Ophthalmology & Visual Science
|January 2, 2007
Summary
Tear trypsin inhibitory capacity (T-TIC) is reduced in vernal keratoconjunctivitis (VKC) patients, while matrix metalloproteinase (MMP)-1 and -9 activity is increased. This local decrease in T-TIC may contribute to prolonged conjunctival inflammation in VKC.
Area of Science:
- Ophthalmology
- Immunology
- Biochemistry
Background:
- Vernal keratoconjunctivitis (VKC) is a bilateral, itching, seasonal eye inflammation.
- Matrix metalloproteinases (MMPs) are enzymes involved in tissue remodeling and inflammation.
- Alpha-1 antitrypsin (AAT) is a key inhibitor of proteases, including MMPs.
Purpose of the Study:
- To investigate tear trypsin inhibitory capacity (T-TIC) and serum trypsin inhibitory capacity (S-TIC) in VKC patients.
- To determine the relationship between T-TIC, S-TIC, and MMP-1 and MMP-9 levels in VKC.
- To explore the role of these factors in the pathogenesis of VKC.
Main Methods:
- In vitro assessment of MMP-1 and MMP-9 inactivation of AAT.
- Collection and analysis of tear samples from VKC patients and healthy controls.
- Quantification of T-TIC, S-TIC, and tear MMP-1 and MMP-9 levels using spectrophotometry and ELISA.
Main Results:
- MMP-1 and MMP-9 were found to inactivate AAT in vitro.
- VKC patients exhibited significantly higher S-TIC and lower T-TIC compared to controls.
- Elevated tear levels and activity of MMP-1 and MMP-9 were observed in VKC patients.
Conclusions:
- T-TIC is reduced, and MMP-1 and MMP-9 activity is increased in the tears of VKC patients.
- A local deficiency in T-TIC may exacerbate or prolong conjunctival inflammation in VKC.
- While T-TIC did not correlate with disease severity, its reduction suggests a role in VKC pathogenesis.