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Ex vivo perfusion of plasma over protein A columns in human mammary adenocarcinoma. Evidence for a protein A leaking by radioimmunoassay
Author(s) -
KINET J. P.,
HUNT J.,
FOIDART J. B.,
DESOROUX A.,
MAHIEU Ph.
Publication year - 1986
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1111/j.1365-2362.1986.tb01306.x
Subject(s) - radioimmunoassay , ex vivo , chills , in vivo , medicine , coefficient of variation , blood proteins , perfusion , chemistry , endocrinology , biology , chromatography , microbiology and biotechnology
. A solid phase radioimmunoassay (RIA) has been developed for detection of protein A in human serum or plasma using plates coated with specific goat anti‐protein A IgG and affinity‐purified anti‐protein A F (ab') 2 fragments labelled with 125 Iodine as a tracer. This RIA detected 25 ng of protein A per ml of serum or plasma. The ‘intra‐plate’ coefficient of variation (CV) was 4·26%, whereas the ‘inter‐plate’ CV was 5·86%, even in the presence of aggregated IgG. The presence of protein A was searched for by this RIA in samples collected during ex vivo perfusion of the plasma of patients suffering from a metastatic mammary adenocarcinoma either over columns of ‘native’ protein A (seven patients; group A) or over columns of protein A in which the Fc‐binding capacity was destroyed (five patients; group B). A protein A leaking occurred with the same incidence (about 20% of the sessions) in both groups. However, major acute side effects (hypotension, chills, mild fever, etc.) and necrolytic responses were seen only in some patients from group A. In these cases, the incidence of side effects, but not of tumoricidal responses, increased with the protein A serum concentrations reached 1 h after the end of the sessions (25–150 ng ml ‐1 ). The data suggest that the therapeutic efficacy of ex vivo protein A immunoadsorption in breast cancer is related to the Fc‐binding capacity of the columns rather than to a leakage of ‘native’ protein A into the blood stream.