TY - JOUR
T1 - Novel non-radioisotope immunoprecipitation studies indicate involvement of pemphigus vulgaris antigen in paraneoplastic pemphigus
AU - Hashimoto, T.
AU - Amagai, M.
AU - Ning, W.
AU - Nishikawa, T.
AU - Karashima, T.
AU - Mori, O.
AU - Jablonska, S.
AU - Chorzelski, T. P.
N1 - Funding Information:
We gratefully appreciate Dr Feliks Wasik, Wroclaw, Poland, Adam Nowak, Szczecin, Poland, and Dr Siri Chiewchanvit, Chiang Mai, Thailand for generously providing PNP sera. We also thank Dr D.R. Garrod, Manchester University for mAb, and Miss M. Makino for technical assistance. We are indebted to Dr Sa. Tsukita and Dr Sh. Tsukita, Kyoto, Japan, for the information of the cell surface biotinylation. This work was supported in part by Grant-in-Aid for Scientific Research from the Ministry of Education, Science and Culture of Japan (04454289), and a grant from the Ministry of Health and Welfare of Japan.
PY - 1998/6
Y1 - 1998/6
N2 - We have developed two different novel immunoprecipitation assays in which radioisotopes are not used, and have examined antigens for four cases of paraneoplastic pemphigus (PNP) including three new patients. The PNP sera showed a clear reactivity with transitional epithelia of rat urinary bladder by immunofluorescence, and reacted with a characteristic doublet of the 210 and 190 kD proteins by immunoblotting of normal human epidermal extract, confirming the diagnosis of PNP. In addition, by immunoprecipitation using silver-stain to detect immunoprecipitated proteins, the PNP sera detected the 250, 210 and 190 kD proteins, while control bullous pemphigoid sera detected only the 230 kD bullous pemphigoid antigen. Furthermore, with another immunoprecipitation using cell surface biotinylation, three of the four PNP sera specifically reacted with the 130 kD pemphigus vulgaris antigen (Dsg3), indicating that pemphigus vulgaris antigen may be involved in PNP. This reactivity was further suggested by the immunoblot analysis using recombinant pemphigus vulgaris antigen. In future, these non-radioisotope immunoprecipitation assays should become a useful tool not only to unravel the complex situation for the PNP antigens, but also to study antigens in other autoimmune bullous skin diseases.
AB - We have developed two different novel immunoprecipitation assays in which radioisotopes are not used, and have examined antigens for four cases of paraneoplastic pemphigus (PNP) including three new patients. The PNP sera showed a clear reactivity with transitional epithelia of rat urinary bladder by immunofluorescence, and reacted with a characteristic doublet of the 210 and 190 kD proteins by immunoblotting of normal human epidermal extract, confirming the diagnosis of PNP. In addition, by immunoprecipitation using silver-stain to detect immunoprecipitated proteins, the PNP sera detected the 250, 210 and 190 kD proteins, while control bullous pemphigoid sera detected only the 230 kD bullous pemphigoid antigen. Furthermore, with another immunoprecipitation using cell surface biotinylation, three of the four PNP sera specifically reacted with the 130 kD pemphigus vulgaris antigen (Dsg3), indicating that pemphigus vulgaris antigen may be involved in PNP. This reactivity was further suggested by the immunoblot analysis using recombinant pemphigus vulgaris antigen. In future, these non-radioisotope immunoprecipitation assays should become a useful tool not only to unravel the complex situation for the PNP antigens, but also to study antigens in other autoimmune bullous skin diseases.
KW - Autoantigen
KW - Immunoblotting
KW - Immunoprecipitation
KW - Paraneoplastic pemphigus
KW - Pemphigus vulgaris antigen
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U2 - 10.1016/S0923-1811(98)00005-X
DO - 10.1016/S0923-1811(98)00005-X
M3 - Article
C2 - 9673895
AN - SCOPUS:0031748891
SN - 0923-1811
VL - 17
SP - 132
EP - 139
JO - Journal of Dermatological Science
JF - Journal of Dermatological Science
IS - 2
ER -