Extracellular Granzymes A and B in Humans: Detection of Native Species During CTL Responses In Vitro and In Vivo

Author:

Spaeny-Dekking Elisabeth H. A.1,Hanna William L.2,Wolbink Angela M.1,Wever Peter C.3,Kummer Alain J.4,Swaak Anton J. G.5,Middeldorp Jaap M.6,Huisman Han G.1,Froelich Christopher J.2,Hack C. Erik1

Affiliation:

1. *Central Laboratory of The Netherlands Red Cross Blood Transfusion Service and the Laboratory for Clinical and Experimental Immunology, and

2. ‡Department of Research, Evanston Hospital, Northwestern University, Evanston, IL 60201;

3. †Department of Internal Medicine, Renal Transplant Unit, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands;

4. §Department of Pathology, Free University Hospital, Amsterdam, The Netherlands;

5. ¶Department of Rheumatology, Daniel Den Hoed Clinic, Rotterdam, The Netherlands; and

6. ∥Organon Technika, Boxtel, The Netherlands

Abstract

AbstractActivated CTLs and NK cells induce apoptosis via multiple mechanisms, including that termed granule exocytosis. The latter pathway consists of vectorial secretion of perforin and a family of granule-associated serine proteases (granzymes) to the target cell. To establish whether granzymes are released extracellularly during cytolytic reactions in vivo, ELISAs that measure the native enzymes were developed and were found to specifically detect granzyme A (GrA) and granzyme B (GrB) at picogram concentrations. Low levels of GrA and GrB were present in plasma of healthy individuals (GrA, 33.5 pg/ml (median); GrB, 11.5 pg/ml (median)), whereas significantly higher levels were present in patients with ongoing CTL response, i.e., patients suffering from infections by EBV or HIV type 1. Markedly elevated levels were also noted in synovial fluid of patients with active rheumatoid arthritis. The measurement of soluble granzymes should be useful to assess clinical disorders associated with activated CTL and NK cells. Furthermore, these results suggest that granzymes mediate biologic effects beyond their described role in apoptotic cell death.

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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