Neurology®
The most widely read and highly cited peer-reviewed Neurology journal
Quick Search
Advanced Search
This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hurko, O.
Right arrow Articles by Walsh, F. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hurko, O.
Right arrow Articles by Walsh, F. S.
NEUROLOGY 1983;33:737
© 1983 American Academy of Neurology

Human fetal muscle-specific antigen is restricted to regenerating myofibers in diseased adult muscle

Orest Hurko, MD and Frank S. Walsh, PhD

Muscular Dystrophy Laboratories, Institute of Neurology, London, England.

A monoclonal antibody, 5.1H11, directed against human fetal muscle and myogenic cells in tissue culture, was used for immunofluorescence analysis of frozen sections of muscle biopsies from 24 patients with different diseases of muscle. The staining pattern was highly specific; detectable levels of the 5.1H11 antigen were restricted to regenerating myofibers as assessed by comparison with serial sections stained with hematoxylineosin. There was no appreciable staining of intrafusal, normal adult extra fusal, denervated, degenerating, or necrotic muscle fibers. Thus, the 5.1H11 antibody allows unambiguous identification of regenerating myofibers in biopsy specimens.

Address correspondence and reprint requests to Dr. Walsh, Muscular Dystrophy Labs, Institute of Neurology, Queen Square, London WC1N 3BG, England.

This work was supported by grants from the Muscular Dystrophy Group of Great Britain. Orest Hurko is the William O. Moseley, Jr., Travelling Fellow of Harvard University.

Accepted for publication September 20, 1982.




This article has been cited by other articles:


Home page
J. Virol.Home page
C. Volpers, C. Thirion, V. Biermann, S. Hussmann, H. Kewes, P. Dunant, H. von der Mark, A. Herrmann, S. Kochanek, and H. Lochmuller
Antibody-Mediated Targeting of an Adenovirus Vector Modified To Contain a Synthetic Immunoglobulin G-Binding Domain in the Capsid
J. Virol., February 1, 2003; 77(3): 2093 - 2104.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
R. Massa, B. Weller, G. Karpati, E. Shoubridge, and S. Carpenter
Familial Inclusion Body Myositis Among Kurdish-Iranian Jews
Arch Neurol, May 1, 1991; 48(5): 519 - 522.
[Abstract] [PDF]


Home page
ScienceHome page
H. Blau, G. Pavlath, E. Hardeman, C. Chiu, L Silberstein, S. Webster, S. Miller, and C Webster
Plasticity of the differentiated state
Science, November 15, 1985; 230(4727): 758 - 766.
[Abstract] [PDF]