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PMID: 945140 Published · ppublish English Journal Article

Anti-actin specificity of human smooth muscle antibodies in chronic active hepatitis.

Clinical and experimental immunology ·Vol. 24 ·No. 2 ·1976-05-00 ·Pages 266-72

Lidman K, Biberfeld G, Fagraeus A, Norberg R, Torstensson R, Utter G, Carlsson L, Luca J, Lindberg U

Abstract

Thirty sera reacting by IFL technique in titres greater than or equal to 100 with smooth muscle fibres of rat stomach, rat renal glomeruli, and with the membrane region of thyroid cells were randomly chosen among sera sent in for routine testing of tissue antibodies. All sera but one were found to be derived from patients with chronic active hepatitis. The smooth muscle and other relevant cell staining were abolished after absorption of sera with actin, prepared from rabbit skeletal muscle and found to be homogeneous by SDS gel-electrophoresis and by electron microscopy. The actin anti-bodies were purified by precipitation of sera with F-actin and elution of the precipitates at acid pH. The purified antibodies stained all tissues in the same way as the original sera. In double immunodiffusion tests all thirty sera gave precipitation with actin. Thus, it was concluded that these broad-reacting SMA are directed against actin. The finding of high-titred SMA is of diagnostic value and supports the clinical diagnosis of active chronic hepatitis. In addition, anti-actin antibodies eluted from human sera are a suitable tool for studying actin-containing cellular structures.

MeSH Terms
Actins/immunology Animals Antibody Specificity Hepatitis/immunology Humans In Vitro Techniques Muscle, Smooth/immunology Rabbits
Chemicals
Actins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Lidman K
Biberfeld G
Fagraeus A
Norberg R
Torstensson R
Utter G
Carlsson L
Luca J
Lindberg U
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Article Info
Journal
Clinical and experimental immunology
Abbr.
Clin Exp Immunol
ISSN
0009-9104
Published
1976-05-00
Pages
266-72
Language
English
Region
England
NLM ID
0057202
PMCID
PMC1538403
Subset
IM
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