Specific Immunoassay Reveals Increased Serum Trypsinogen 3 in Acute Pancreatitis

Author:

Oiva Jani1,Itkonen Outi23,Koistinen Riitta3,Hotakainen Kristina3,Zhang Wang-Ming4,Kemppainen Esko1,Puolakkainen Pauli1,Kylänpää Leena1,Stenman Ulf-Håkan1,Koistinen Hannu3

Affiliation:

1. Department of Surgery and

2. Laboratory Division (HUSLAB), Helsinki University Central Hospital, Helsinki, Finland

3. Department of Clinical Chemistry, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland

4. Department of Clinical Pathology, Cleveland Clinic, Cleveland, OH

Abstract

BACKGROUND Trypsinogen 3 is a minor trypsinogen isoform in the pancreas. In contrast with trypsin 1 and 2, trypsin 3 degrades pancreatic secretory trypsin inhibitor, which may lead to an excess of active trypsin and acute pancreatitis (AP). We developed an immunoassay for trypsinogen 3 and studied whether an assay of serum trypsinogen 3 is of clinical utility in the diagnosis of AP. METHODS Monoclonal antibodies were generated using recombinant human trypsinogen 3 as the antigen and used to establish a sandwich-type immunoassay. We analyzed serum trypsinogen 3 concentrations in 82 patients with AP and 63 patients with upper abdominal pain (controls). The reference interval was determined using serum samples from 172 apparently healthy individuals. RESULTS The measuring range of the trypsinogen 3 assay was 1.0–250 μg/L. Intra- and interassay CVs were <11%, and cross-reactivity with other trypsinogen isoenzymes was <0.1%. The median trypsinogen 3 concentration in serum from healthy individuals was <1.0 μg/L, and the upper reference limit was 4.4 μg/L. We observed increased trypsinogen 3 concentrations in patients with mild (median 9.5 μg/L) and severe (15.0 μg/L) AP; in both groups, the concentrations were significantly higher than in controls (median <1.0 μg/L) (P < 0.0001). In ROC analysis, the area under the curve of trypsinogen 3 for separation between AP and controls was 0.90 (P < 0.0001). CONCLUSIONS We established for the first time a specific immunoassay for trypsinogen 3 using monoclonal antibodies. Patients with AP were found to have increased serum concentrations of trypsinogen 3. The availability of this assay will be useful for studies of the clinical utility of trypsinogen 3.

Funder

Helsinki University Central Hospital

Finnish Cancer Foundation

Academy of Finland

Finnish Funding Agency for Technology and Innovation

Finska Läkaresällskapet

Clinical Chemistry Research Foundation

Finnish Cultural Foundation

Research Foundation of Abdominal Illnesses

Professor MI Turunen Foundation

Maud Kuistila Foundation

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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