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A Monoclonal Antibody against the Paraneoplastic Pemphigus (PNP) Antigen, Envoplakin: cDNA Sequences Encoding the Variable Regions of Heavy and Light Chains

Authors
 Jin-Hyung Ahn  ;  Min-Geol Lee  ;  Tae Ho Lee  ;  Soo-Chan Kim 
Citation
 MOLECULES AND CELLS, Vol.18(2) : 237-241, 2004 
Journal Title
MOLECULES AND CELLS
ISSN
 1016-8478 
Issue Date
2004
MeSH
Animals ; Antibodies, Monoclonal/biosynthesis ; Antibodies, Monoclonal/genetics* ; Antibody Specificity ; Base Sequence ; Cloning, Molecular/methods ; DNA, Complementary ; Humans ; Hybridomas/immunology ; Immune Sera ; Immunoassay ; Immunoglobulin Heavy Chains/genetics ; Immunoglobulin Light Chains/genetics ; Keratinocytes/chemistry ; Keratinocytes/ultrastructure ; Membrane Proteins/immunology* ; Mice ; Molecular Sequence Data ; Paraneoplastic Syndromes/genetics* ; Pemphigus ; Protein Precursors/immunology*
Keywords
Envoplakin ; Monoclonal Antibody ; Paraneoplastic Pemphigus (PNP)
Abstract
Paraneoplastic pemphigus (PNP) is an acquired autoimmune disorder characterized by severe mucosal erosion, and polymorphous cutaneous lesions associated with neoplasia. PNP patients have circulating autoantibodies that bind to stratified and nonstratified epithelia. Previously, we showed that envoplakin was a component of the antigen complex recognized by PNP sera. In the present study we generated a monoclonal antibody, EVP-YS, against human envoplakin. The antibody bound to keratinocyte cell surfaces and reacted with the 210-kDa PNP antigen, confirming its specificity for envoplakin. The variable regions of the heavy (H) and light (L) chain genes were cloned from the hybridoma and shown to belong to mouse H chain subgroup III and k light chain subgroup V, respectively. The L chain of EVP-YS was 98% identical to the k chains of some autoantibodies and anti-nucleic acid antibodies, and had an identical amino acid sequence in all three complementary determining regions, suggesting that the H chains determine the specificity of the EVP-YS-envoplakin interaction. The EVP-YS antibody can be used to evaluate the sensitivity and specificity of clinical, histological, and immunological criteria for diagnosing PNP.
Files in This Item:
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Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Soo Chan(김수찬) ORCID logo https://orcid.org/0000-0002-2327-4755
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/112850
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