학술논문

Functional analysis and quantification of the complement C3 derived anaphylatoxin C3a with a monoclonal antibody.
Document Type
Article
Source
Clinical & Experimental Immunology. Jun1987, Vol. 68 Issue 3, p703-711. 9p.
Subject
*MONOCLONAL antibodies
*TOXINS
*ADULT respiratory distress syndrome
*RESPIRATORY diseases
*ENZYME-linked immunosorbent assay
*IMMUNOPATHOLOGY
Language
ISSN
0009-9104
Abstract
The C3 fragment C3a belongs to the anaphylatoxins. It has immune regulatory activity and contributes to the pathogenesis of the adult respiratory distress syndrome (ARDS). The low molecular weight (9 kD) of C3a complicates the production of antibodies to C3a. We obtained a monoclonal antibody (designated HI3) to human C3a. It reacts with C3a or C3a-desArg and with native C3 but not with C5 or C5a. In immunoblot analysis it reacts with the α-but not with β-chain of C3 and binds to a protein with a mol. wt of about 10 kD present in zymosan-activated sera which is only marginally detectable in nonactivated serum and absent in plasma. H13 crossreacts with the analogous proteins of rabbit, guinea pig and sheep. H13 has the capacity to bind 125I-radiolabelled C3a efficiently but fails totally to react with 125I-C5a or with other C3 α-chain fragments. H13 blocks C3a functional activity. It markedly inhibits C3a-induced ³H-serotonin release from platelets in vitro and similarly inhibits the C3a-induced extravasation of Evans blue into the skin in vivo. H13 does not interfere with the haemolytic activity orC3. An ELISA system was established using H13 which permits quantification of C3a in sera of polytrauma patients. The antibody H13 should facilitate further functional analysis of C3a in experimental systems. It should be useful for quantification of C3a in diagnostic assays and also for application in immunopathology. [ABSTRACT FROM AUTHOR]