Autoimmune reactivity against precursor form of desmoglein 1 in healthy Tunisians in the area of endemic pemphigus foliaceus

Amina Toumi, Marwah Adly Saleh, Jun Yamagami, Olfa Abida, Maryem Kallel, Abderrahmen Masmoudi, Sondes Makni, Hamida Turki, Takahisa Hachiya, Keiko Kuroda, John R. Stanley, Hatem Masmoudi, Masayuki Amagai

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Background: Desmoglein 1 (Dsg1), the pemphigus foliaceus (PF) antigen, is produced as a precursor (preDsg1) and is transported to the cell surface as the mature form (matDsg1). Recent studies show that B cells from North American individuals without pemphigus can potentially produce anti-preDsg1 IgG antibodies, but ELISA screening of large numbers of normal people in North America and Japan hardly ever shows circulating antibodies against preDsg1 or matDsg1. In contrast, in Tunisia, where PF is endemic, anti-Dsg1 IgGs are frequently detected in healthy individuals. Objective: To characterize these anti-Dsg1 antibodies from normal individuals in Tunisia. Methods: Sera from 16 healthy individuals and 9 PF patients in the endemic PF area in Tunisia, and sera from Japanese non-endemic PF patients were analyzed by immunoprecipitation-immunoblotting using recombinant proteins of preDsg1, matDsg1, and domain-swapped Dsg1/Dsg2 molecules. Results: Sera from normal Tunisian individuals reacted to preDsg1 alone (8/16) or more strongly to preDsg1 than to matDsg1 (7/16), while those from all Tunisian PF patients and Japanese non-endemic PF patients reacted similarly to preDsg1 and matDsg1, or preferentially to matDsg1. The epitopes recognized by anti-Dsg1 IgGs from normal Tunisian individuals were more frequently found in the C-terminal extracellular domains (EC3 to EC5), while those in Tunisian endemic PF patients were more widely distributed throughout the extracellular domains, suggesting IgGs against EC1 and EC2 developed during disease progression. Conclusions: These findings indicate that IgG autoantibodies against Dsg1 are mostly raised against preDsg1 and/or C-terminal domains of Dsg1 in healthy Tunisians in the endemic area of PF.

Original languageEnglish
Pages (from-to)19-25
Number of pages7
JournalJournal of Dermatological Science
Volume70
Issue number1
DOIs
Publication statusPublished - 2013 Apr

Fingerprint

Desmoglein 1
Pemphigus
Tunisia
Antibodies
Serum
Pemphigus and fogo selvagem
North America
Immunoprecipitation
Recombinant Proteins
Immunoblotting
Autoantibodies
Disease Progression
Epitopes
Japan
Screening
B-Lymphocytes
Immunoglobulin G
Enzyme-Linked Immunosorbent Assay
Cells

Keywords

  • Autoantibody
  • Desmoglein 1
  • Pemphigus foliaceus
  • Precursor

ASJC Scopus subject areas

  • Dermatology
  • Biochemistry
  • Molecular Biology

Cite this

Autoimmune reactivity against precursor form of desmoglein 1 in healthy Tunisians in the area of endemic pemphigus foliaceus. / Toumi, Amina; Saleh, Marwah Adly; Yamagami, Jun; Abida, Olfa; Kallel, Maryem; Masmoudi, Abderrahmen; Makni, Sondes; Turki, Hamida; Hachiya, Takahisa; Kuroda, Keiko; Stanley, John R.; Masmoudi, Hatem; Amagai, Masayuki.

In: Journal of Dermatological Science, Vol. 70, No. 1, 04.2013, p. 19-25.

Research output: Contribution to journalArticle

Toumi, A, Saleh, MA, Yamagami, J, Abida, O, Kallel, M, Masmoudi, A, Makni, S, Turki, H, Hachiya, T, Kuroda, K, Stanley, JR, Masmoudi, H & Amagai, M 2013, 'Autoimmune reactivity against precursor form of desmoglein 1 in healthy Tunisians in the area of endemic pemphigus foliaceus', Journal of Dermatological Science, vol. 70, no. 1, pp. 19-25. https://doi.org/10.1016/j.jdermsci.2013.02.002
Toumi, Amina ; Saleh, Marwah Adly ; Yamagami, Jun ; Abida, Olfa ; Kallel, Maryem ; Masmoudi, Abderrahmen ; Makni, Sondes ; Turki, Hamida ; Hachiya, Takahisa ; Kuroda, Keiko ; Stanley, John R. ; Masmoudi, Hatem ; Amagai, Masayuki. / Autoimmune reactivity against precursor form of desmoglein 1 in healthy Tunisians in the area of endemic pemphigus foliaceus. In: Journal of Dermatological Science. 2013 ; Vol. 70, No. 1. pp. 19-25.
@article{6a162a89e62349e48b25c9516862a4bb,
title = "Autoimmune reactivity against precursor form of desmoglein 1 in healthy Tunisians in the area of endemic pemphigus foliaceus",
abstract = "Background: Desmoglein 1 (Dsg1), the pemphigus foliaceus (PF) antigen, is produced as a precursor (preDsg1) and is transported to the cell surface as the mature form (matDsg1). Recent studies show that B cells from North American individuals without pemphigus can potentially produce anti-preDsg1 IgG antibodies, but ELISA screening of large numbers of normal people in North America and Japan hardly ever shows circulating antibodies against preDsg1 or matDsg1. In contrast, in Tunisia, where PF is endemic, anti-Dsg1 IgGs are frequently detected in healthy individuals. Objective: To characterize these anti-Dsg1 antibodies from normal individuals in Tunisia. Methods: Sera from 16 healthy individuals and 9 PF patients in the endemic PF area in Tunisia, and sera from Japanese non-endemic PF patients were analyzed by immunoprecipitation-immunoblotting using recombinant proteins of preDsg1, matDsg1, and domain-swapped Dsg1/Dsg2 molecules. Results: Sera from normal Tunisian individuals reacted to preDsg1 alone (8/16) or more strongly to preDsg1 than to matDsg1 (7/16), while those from all Tunisian PF patients and Japanese non-endemic PF patients reacted similarly to preDsg1 and matDsg1, or preferentially to matDsg1. The epitopes recognized by anti-Dsg1 IgGs from normal Tunisian individuals were more frequently found in the C-terminal extracellular domains (EC3 to EC5), while those in Tunisian endemic PF patients were more widely distributed throughout the extracellular domains, suggesting IgGs against EC1 and EC2 developed during disease progression. Conclusions: These findings indicate that IgG autoantibodies against Dsg1 are mostly raised against preDsg1 and/or C-terminal domains of Dsg1 in healthy Tunisians in the endemic area of PF.",
keywords = "Autoantibody, Desmoglein 1, Pemphigus foliaceus, Precursor",
author = "Amina Toumi and Saleh, {Marwah Adly} and Jun Yamagami and Olfa Abida and Maryem Kallel and Abderrahmen Masmoudi and Sondes Makni and Hamida Turki and Takahisa Hachiya and Keiko Kuroda and Stanley, {John R.} and Hatem Masmoudi and Masayuki Amagai",
year = "2013",
month = "4",
doi = "10.1016/j.jdermsci.2013.02.002",
language = "English",
volume = "70",
pages = "19--25",
journal = "Journal of Dermatological Science",
issn = "0923-1811",
publisher = "Elsevier Ireland Ltd",
number = "1",

}

TY - JOUR

T1 - Autoimmune reactivity against precursor form of desmoglein 1 in healthy Tunisians in the area of endemic pemphigus foliaceus

AU - Toumi, Amina

AU - Saleh, Marwah Adly

AU - Yamagami, Jun

AU - Abida, Olfa

AU - Kallel, Maryem

AU - Masmoudi, Abderrahmen

AU - Makni, Sondes

AU - Turki, Hamida

AU - Hachiya, Takahisa

AU - Kuroda, Keiko

AU - Stanley, John R.

AU - Masmoudi, Hatem

AU - Amagai, Masayuki

PY - 2013/4

Y1 - 2013/4

N2 - Background: Desmoglein 1 (Dsg1), the pemphigus foliaceus (PF) antigen, is produced as a precursor (preDsg1) and is transported to the cell surface as the mature form (matDsg1). Recent studies show that B cells from North American individuals without pemphigus can potentially produce anti-preDsg1 IgG antibodies, but ELISA screening of large numbers of normal people in North America and Japan hardly ever shows circulating antibodies against preDsg1 or matDsg1. In contrast, in Tunisia, where PF is endemic, anti-Dsg1 IgGs are frequently detected in healthy individuals. Objective: To characterize these anti-Dsg1 antibodies from normal individuals in Tunisia. Methods: Sera from 16 healthy individuals and 9 PF patients in the endemic PF area in Tunisia, and sera from Japanese non-endemic PF patients were analyzed by immunoprecipitation-immunoblotting using recombinant proteins of preDsg1, matDsg1, and domain-swapped Dsg1/Dsg2 molecules. Results: Sera from normal Tunisian individuals reacted to preDsg1 alone (8/16) or more strongly to preDsg1 than to matDsg1 (7/16), while those from all Tunisian PF patients and Japanese non-endemic PF patients reacted similarly to preDsg1 and matDsg1, or preferentially to matDsg1. The epitopes recognized by anti-Dsg1 IgGs from normal Tunisian individuals were more frequently found in the C-terminal extracellular domains (EC3 to EC5), while those in Tunisian endemic PF patients were more widely distributed throughout the extracellular domains, suggesting IgGs against EC1 and EC2 developed during disease progression. Conclusions: These findings indicate that IgG autoantibodies against Dsg1 are mostly raised against preDsg1 and/or C-terminal domains of Dsg1 in healthy Tunisians in the endemic area of PF.

AB - Background: Desmoglein 1 (Dsg1), the pemphigus foliaceus (PF) antigen, is produced as a precursor (preDsg1) and is transported to the cell surface as the mature form (matDsg1). Recent studies show that B cells from North American individuals without pemphigus can potentially produce anti-preDsg1 IgG antibodies, but ELISA screening of large numbers of normal people in North America and Japan hardly ever shows circulating antibodies against preDsg1 or matDsg1. In contrast, in Tunisia, where PF is endemic, anti-Dsg1 IgGs are frequently detected in healthy individuals. Objective: To characterize these anti-Dsg1 antibodies from normal individuals in Tunisia. Methods: Sera from 16 healthy individuals and 9 PF patients in the endemic PF area in Tunisia, and sera from Japanese non-endemic PF patients were analyzed by immunoprecipitation-immunoblotting using recombinant proteins of preDsg1, matDsg1, and domain-swapped Dsg1/Dsg2 molecules. Results: Sera from normal Tunisian individuals reacted to preDsg1 alone (8/16) or more strongly to preDsg1 than to matDsg1 (7/16), while those from all Tunisian PF patients and Japanese non-endemic PF patients reacted similarly to preDsg1 and matDsg1, or preferentially to matDsg1. The epitopes recognized by anti-Dsg1 IgGs from normal Tunisian individuals were more frequently found in the C-terminal extracellular domains (EC3 to EC5), while those in Tunisian endemic PF patients were more widely distributed throughout the extracellular domains, suggesting IgGs against EC1 and EC2 developed during disease progression. Conclusions: These findings indicate that IgG autoantibodies against Dsg1 are mostly raised against preDsg1 and/or C-terminal domains of Dsg1 in healthy Tunisians in the endemic area of PF.

KW - Autoantibody

KW - Desmoglein 1

KW - Pemphigus foliaceus

KW - Precursor

UR - http://www.scopus.com/inward/record.url?scp=84875808545&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84875808545&partnerID=8YFLogxK

U2 - 10.1016/j.jdermsci.2013.02.002

DO - 10.1016/j.jdermsci.2013.02.002

M3 - Article

VL - 70

SP - 19

EP - 25

JO - Journal of Dermatological Science

JF - Journal of Dermatological Science

SN - 0923-1811

IS - 1

ER -