Identification and characterization of autoreactive T cell responses to bullous pemphigoid antigen 2 in patients and healthy controls

被引:179
作者
Büdinger, L
Borradori, L
Yee, C
Eming, R
Ferencik, S
Grosse-Wilde, H
Merk, HF
Yancey, K
Hertl, M
机构
[1] Rhein Westfal TH Klinikum, Hautklin, D-52074 Aachen, Germany
[2] Univ Geneva, Hop Cantonal, Dermatol Clin, CH-1211 Geneva, Switzerland
[3] NCI, Dermatol Branch, Bethesda, MD 20892 USA
[4] Univ Essen Gesamthsch Klinikum, Inst Immunol, D-45122 Essen, Germany
关键词
hemidesmosome; extracellular domain; autoreactive Th1/Th2 cells; cytokines; HLA class II restriction;
D O I
10.1172/JCI3335
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Antibodies against the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) are thought to play a key role in the pathogenesis of bullous pemphigoid (BP), the most frequent autoimmune bullous disease of the skin. Autoreactive T cell responses to BPAG2 were investigated in 16 BP patients and 24 healthy controls by coculture of PBMC with two recombinant BPAG2 proteins (extracellular domain of BPAG2). Primary in vitro T cell responses to BPAG2 were observed in 10/12 BP patients expressing the BP-associated HLA-DQB1*0301 allele and 8/10 DQB1*0301 positive healthy individuals. DQB1*0301 also restricted three autoreactive T cell lines from two BP patients and a healthy donor. In contrast, PBMC from 14 normal patients carrying HLA class II alleles other than DQB1*0301 were not stimulated by BPAG2. Autoreactive BPAG2-specific CD4(+) T cell lines and clones from five BP patients produced both Th1 and Th2 cytokines, whereas three autoreactive T cell lines from three DQB1*0301 positive normal patients produced exclusively IFN-gamma. The absence of BPAG2-specific Th2 cells in healthy individuals strongly suggests that autoreactive Th2 responses to BPAG2 are restricted to BP patients and may thus be critical in the pathogenesis of BP.
引用
收藏
页码:2082 / 2089
页数:8
相关论文
共 41 条
  • [1] MAJOR HISTOCOMPATIBILITY COMPLEX HAPLOTYPE STUDIES IN ASHKENAZI JEWISH PATIENTS WITH PEMPHIGUS-VULGARIS
    AHMED, AR
    YUNIS, EJ
    KHATRI, K
    WAGNER, R
    NOTANI, G
    AWDEH, Z
    ALPER, CA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (19) : 7658 - 7662
  • [2] Cicatricial pemphigoid autoantibodies react with multiple sites on the BP180 extracellular domain
    Balding, SD
    Prost, C
    Diaz, LA
    Bernard, P
    Bedane, C
    Aberdam, D
    Giudice, GJ
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (01) : 141 - 146
  • [3] Bernard P, 1990, CLIN IMMUNOL IMMUNOP, V54, P489
  • [4] SUBCLASS DISTRIBUTION OF IGG AUTOANTIBODIES IN BULLOUS PEMPHIGOID
    BIRD, P
    FRIEDMANN, PS
    LING, N
    BIRD, AG
    THOMPSON, RA
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 86 (01) : 21 - 25
  • [5] The localization of bullous pemphigoid antigen 180 (BP180) in hemidesmosomes is mediated by its cytoplasmic domain and seems to be regulated by the beta 4 integrin subunit
    Borradori, L
    Koch, PJ
    Niessen, CM
    Erkeland, S
    vanLeusden, MR
    Sonnenberg, A
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 136 (06) : 1333 - 1347
  • [6] INVITRO PROLIFERATIVE RESPONSES AND ANTIBODY-TITERS SPECIFIC TO HUMAN ACETYLCHOLINE-RECEPTOR SYNTHETIC PEPTIDES IN PATIENTS WITH MYASTHENIA-GRAVIS AND RELATION TO HLA CLASS-II GENES
    BROCKE, S
    BRAUTBAR, C
    STEINMAN, L
    ABRAMSKY, O
    ROTHBARD, J
    NEUMANN, D
    FUCHS, S
    MOZES, E
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (06) : 1894 - 1900
  • [7] Delaporte E, 1996, J IMMUNOL, V157, P3642
  • [8] A common major histocompatibility complex class II allele HLA-DQB1*0301 is present in clinical variants of pemphigoid
    Delgado, JC
    Turbay, D
    Yunis, EJ
    Yunis, JJ
    Morton, ED
    Bhol, K
    Norman, R
    Alper, CA
    Good, RA
    Ahmed, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) : 8569 - 8571
  • [9] FREDRIKSON S, 1993, J IMMUNOL, V151, P2217
  • [10] HUMAN B-CELL CLONES CAN BE INDUCED TO PROLIFERATE AND TO SWITCH TO IGE AND IGG4 SYNTHESIS BY INTERLEUKIN-4 AND A SIGNAL PROVIDED BY ACTIVATED CD4+ T-CELL CLONES
    GASCAN, H
    GAUCHAT, JF
    RONCAROLO, MG
    YSSEL, H
    SPITS, H
    DEVRIES, JE
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) : 747 - 750