You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 125 No. 4, April 1989 TABLE OF CONTENTS
  Archives
  •  Online Features
  ARTICLES
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

19-DEJ-1, A Hemidesmosome-Anchoring Filament Complex-Associated Monoclonal Antibody

Definition of a New Skin Basement Membrane Antigenic Defect in Junctional and Dystrophic Epidermolysis Bullosa

Jo-David Fine, MD; Yuji Horiguchi, MD; John R. Couchman, PhD

Arch Dermatol. 1989;125(4):520-523.


Abstract

• A murine monoclonal antibody (19-DEJ-1) was recently produced that recognizes a unique antigenic epitope of human skin basement membrane localized to the midlamina lucida exclusively in those areas bordered by overlying hemidesmosomes. To determine whether the antigen defined by 19-DEJ-1 is normally expressed in one or more forms of epidermolysis bullosa (EB) known to have structural and antigenic defects in skin basement membrane, we examined by indirect immunofluorescence 46 specimens of clinically normal skin from 43 patients representing each of the four forms of inherited EB (simplex, 15 patients; junctional, nine patients; dominant dystrophic, seven patients; and recessive dystrophic, 15 patients). All nine junctional EB specimens revealed absent 19-DEJ-1 binding; similarly, seven of 15 and one of six recessive and dominant dystrophic EB skin specimens, respectively, showed lack of antibody recognition. In contrast, binding was normal in 15 of 15 EB simplex specimens and five of six dominant dystrophic EB specimens. Absent binding of 19-DEJ-1 to junctional EB skin correlates well with the localization of this antigen to the region of the midlamina lucida. Its absence in approximately 50% of patients with recessive dystrophic EB further suggests, for the first time, that an inherited defect in basement membrane is shared in patients with junctional and some recessive dystrophic EB. The difference in site of skin cleavage in the latter two disorders gives additional support to the hypothesis that 19-DEJ-1 recognizes a structure, such as the anchoring filament, which both bridges the entire basement membrane and contributes to epidermal-dermal adhesion.

(Arch Dermatol 1989;125:520-523)



Author Affiliations

From the Departments of Dermatology (Drs Fine and Horiguchi), Institute of Dental Research (Dr Fine), and Cell Biology and Anatomy (Dr Couchman), University of Alabama at Birmingham School of Medicine; and Dermatology Section, Medical Service, Birmingham (Ala) Veterans Administration Medical Center (Dr Fine).


Footnotes

Accepted for publication Nov 17, 1988.

Presented at the Southern Regional meeting of the Society for Investigative Dermatology, New Orleans, Feb 4,1988.

Reprint requests to Department of Dermatology, University of Alabama at Birmingham, UAB Station, Box 76, Birmingham, AL 35294 (Dr Fine).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Immunohistochemical, Ultrastructural, and Molecular Features of Kindler Syndrome Distinguish It From Dystrophic Epidermolysis Bullosa
Shimizu et al.
Arch Dermatol 1997;133:1111-1117.
ABSTRACT  

Absence of Detectable {alpha}6 Integrin in Pyloric Atresia-Junctional Epidermolysis Bullosa Syndrome: Application for Prenatal Diagnosis in a Family at Risk for Recurrence
Shimizu et al.
Arch Dermatol 1996;132:919-925.
ABSTRACT  

Generalized Atrophic Benign Epidermolysis Bullosa: Either 180-kd Bullous Pemphigoid Antigen or Laminin-5 Deficiency
Jonkman et al.
Arch Dermatol 1996;132:145-150.
ABSTRACT  

Advances in the Diagnosis of Subepidermal Bullous Diseases
Yancey and Hintner
Arch Dermatol 1996;132:220-222.
ABSTRACT  

The Molecular Genetics of Basement Membrane Diseases
Marinkovich
Arch Dermatol 1993;129:1557-1565.
ABSTRACT  

Type VII Collagen and 19-DEJ-1 Antigen: Comparison of Expression in Inversa and Generalized Variants of Recessive Dystrophic Epidermolysis Bullosa
Fine et al.
Arch Dermatol 1990;126:1587-1593.
ABSTRACT  

19-DEJ-1, a Monoclonal Antibody to the Hemidesmosome-Anchoring Filament Complex, Is the Only Reliable Immunohistochemical Probe for All Major Forms of Junctional Epidermolysis Bullosa
Fine
Arch Dermatol 1990;126:1187-1190.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1989 American Medical Association. All Rights Reserved.