z-logo
Premium
30 Increased Mercury Load in Protein A Immunoadsorption
Author(s) -
Pernat A Marn,
Horvat M,
Logar M,
Ponikvar R
Publication year - 2005
Publication title -
therapeutic apheresis and dialysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.415
H-Index - 53
eISSN - 1744-9987
pISSN - 1744-9979
DOI - 10.1111/j.1526-0968.2005.222_30_30.x
Subject(s) - immunoadsorption , thiomersal , medicine , mercury (programming language) , toxicity , venous blood , immunology , antibody , computer science , programming language
Background  Immunoadsorption is an adsorption technique for extracorporeal removal of circulating autoantibodies in autoimmune diseases such as myasthenia gravis and Guillain‐Barré syndrome. To prevent microbial growth during storage, the protein A columns are primed with thiomersal containing toxic ethylmercury which could be released during the immunoadsorption treatment and potentially result in its accumulation and toxicity. To reduce a thiomersal‐related mercury release during immunoadsorption treatment we introduced a modified rinsing solution containing N‐acetylcysteine which is an avid mercury scavenger. Methods  Thirteen patients were treated by 17 protein A immunoadsorption treatments and venous blood samples were collected immediately before and after each session. Whole blood mercury levels were measured by atomic absorption spectroscopy and ethylmercury levels by atomic fluorescent spectroscopy. According to the manufacturer's recommendations we used 600 mg of N‐acetylcysteine to rinse the mercury from protein‐loaded columns before each immunoadsorption treatment. Results  Following protein A immunoadsorption ethylmercury levels increased from 0.148 ± 0.402 ng/g to 2.026 ± 1.944 ng/g ( P  < 0.001) and whole blood mercury increased from 2.447 ± 3.065 ng/g to 20.437 ± 28.603 ng/g ( P  = 0.02). Post‐treatment values of whole blood mercury exceeded upper safety level of 5 ng/g in all 17 immunoadsorption treatments but no patient developed clinical signs of mercury toxicity. In one patient immunoadsorption treatment was repeated within 7 days and the results of serial determinations of blood mercury levels are shown in Table A30. A30Ethylmercury Whole blood mercury (ng/g) (ng/g)Before IA After IA Before IA After IADay 0 0.13 ± 0.03 1.35 ± 0.12 0.49 ± 0.06 76.8 ± 5.6 Day 1 0.17 ± 0.00 0.10 ± 0.02 8.14 ± 1.24 19.4 ± 0.6 Day 2 0.05 ± 0.00 0.09 ± 0.00 9.57 ± 0.80 11.8 ± 0.9 Day 3 0.03 ± 0.00 0.08 ± 0.01 6.96 ± 0.09 8.52 ± 0.39 Day 7 1.69 ± 0.00 4.23 ± 0.12 5.54 ± 0.32 9.04 ± 0.48Data are presented as means ± standard deviation. IA, immunoadsorption.Conclusions  The results of our study showed that whole blood mercury and ethylmercury levels were increased during the immunoadsorption treatments, suggesting mercury release from thiomersal‐primed columns even with addition of N‐acetylcysteine to the rinsing solution. Mercury release was more pronounced at the beginning of serial immunoadsorption treatments which indicates that mercury exposure might depend on the storage time of protein A columns containing thiomersal priming solution.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here