Levels of anti-BP180 NC16A IgE do not correlate with severity of disease in the early stages of bullous pemphigoid

被引:19
作者
Liu Bing [1 ,2 ]
Zhou Xiping [1 ,2 ]
Li Li [1 ,2 ]
Peng Jun [3 ]
Wang Yi-Xia [4 ]
Yang Min [5 ]
Liu Qing [6 ]
Sun Qiu-Ning [1 ,2 ]
Jin Hong-Zhong [1 ,2 ]
Zuo Ya-Gang [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Dermatol, Beijing 100730, Peoples R China
[2] Peking Union Med Coll, Beijing 100730, Peoples R China
[3] Cangzhou Peoples Hosp, Dept Dermatol, Cangzhou, Hebei Province, Peoples R China
[4] Air Force Gen Hosp, Dept Dermatol, Beijing, Peoples R China
[5] Beijing Hosp, Dept Dermatol, Beijing, Peoples R China
[6] Beijing Hosp Tradit Chinese Med, Dept Dermatol, Beijing, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Bullous pemphigoid; IgE; Anti-BP180NC16A; Sera; Blister fluid; HUMAN SKIN; BP180; AUTOANTIBODIES; AUTOANTIGEN; BP230; MICE;
D O I
10.1007/s00403-015-1598-3
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Bullous pemphigoid (BP), a common autoimmune skin disease, is associated with IgG autoantibodies against the hemidesmosomal proteins, BP180 and BP230. In addition to IgG, IgE has been shown to play a role in the disease. However, the association between disease activity and IgE specific to the NC16A domain of BP180 in blister fluid remains unclear. Our objective was to evaluate the correlation between BP disease activity and BP180 NC16A-specific IgE sera and blister fluid titers, and to analyze changes during treatment. We evaluated the levels of anti-BP180 IgE autoantibodies in the sera and blister fluids of 37 BP patients using an Enzyme-linked immunosorbent assay. We also observed changes in the levels of these antibodies in 2 BP patients at 4 or 5 different time points (day 0 when the patient first visited our hospital, day 5, day 14, day 39 and day 62 for patient 1; day 0, day 4, day 8 and day 17 for patient 2). We also collected extra serum samples from the 2 patients when the disease was controlled (blister disappeared) (day 85, day 104 and day 146 for patient 1 and day 123, day 158 and day 189 for the other patient). IgE anti-BP180 antibodies were detected in the serum of 72.97 % of the patients. There was no correlation between disease activity scores and BP180 NC16A IgE titers in serum (r = -0.077, p > 0.05) or in blister fluid (r = 0.262, p > 0.05). The levels of the autoantibody in serum were positively correlated with that in blister fluid (r = 0.6651, p < 0.001); however, the levels continued to rise despite effective control of the disease in the initial two to 6 weeks of diagnosis. The level of this autoantibody reached a peak on day 39 for patient 1 and on day 17 for patient 2 although the systemic and topical medication of steroid had controlled the disease process effectively. We conclude that levels of anti-BP180 NC16A IgE are higher in the sera than blister fluids. These levels could generally reflect disease severity throughout the course of the disease, but not in the early stages of medication.
引用
收藏
页码:849 / 854
页数:6
相关论文
共 14 条
  • [1] Incidence of bullous pemphigoid and mortality of patients with bullous pemphigoid in Olmsted County, Minnesota, 1960 through 2009
    Brick, Katherine E.
    Weaver, Chad H.
    Lohse, Christine M.
    Pittelkow, Mark R.
    Lehman, Julia S.
    Camilleri, Michael J.
    Al-Hashimi, Mustafa
    Wieland, Carilyn N.
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2014, 71 (01) : 92 - 99
  • [2] Usefulness of BP230 and BP180-NC16a Enzyme-Linked Immunosorbent Assays in the Initial Diagnosis of Bullous Pemphigoid A Retrospective Study of 138 Patients
    Charneux, Julie
    Lorin, Johanna
    Vitry, Fabien
    Antonicelli, Frank
    Reguiai, Ziad
    Barbe, Coralie
    Tabary, Thierry
    Grange, Florent
    Bernard, Philippe
    [J]. ARCHIVES OF DERMATOLOGY, 2011, 147 (03) : 286 - 291
  • [3] A comparative study of antibody titers of blister fluid and serum in patients with subepidermal. immunobullous diseases
    Daneshpazhooh, M
    Shahdi, M
    Aghaeepoor, M
    Hasiri, G
    Chams, C
    [J]. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2004, 43 (05) : 348 - 351
  • [4] A pathogenic role for IgE in autoimmunity: Bullous pemphigoid IgE reproduces the early phase of lesion development in human skin grafted to nu/nu mice
    Fairley, Janet A.
    Burnett, Christopher T.
    Fu, Chang-Ling
    Larson, David L.
    Fleming, Matthew G.
    Giudice, George J.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 (11) : 2605 - 2611
  • [5] Missing the target: Characterization of bullous pemphigoid patients who are negative using the BP180 enzyme-linked immunosorbant assay
    Fairley, Janet A.
    Bream, Matthew
    Fullenkamp, Colleen
    Syrbu, Sergei
    Chen, Mei
    Messingham, Kelly N.
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2013, 68 (03) : 395 - 403
  • [6] IgE recognition of bullous pemphigoid (BP)180 and BP230 in BP patients and elderly individuals with pruritic dermatoses
    Fania, Luca
    Caldarola, Giacomo
    Mueller, Ralf
    Brandt, Oliver
    Pellicano, Riccardo
    Feliciani, Claudio
    Hertl, Michael
    [J]. CLINICAL IMMUNOLOGY, 2012, 143 (03) : 236 - 245
  • [7] GIUDICE GJ, 1993, J IMMUNOL, V151, P5742
  • [8] CLONING AND PRIMARY STRUCTURAL-ANALYSIS OF THE BULLOUS PEMPHIGOID AUTOANTIGEN BP180
    GIUDICE, GJ
    EMERY, DJ
    DIAZ, LA
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (03) : 243 - 250
  • [9] IgG from Patients with Bullous Pemphigoid Depletes Cultured Keratinocytes of the 180-kDa Bullous Pemphigoid Antigen (Type XVII Collagen) and Weakens Cell Attachment
    Iwata, Hiroaki
    Kamio, Naoko
    Aoyama, Yumi
    Yamamoto, Yukari
    Hirako, Yoshiaki
    Owaribe, Katsushi
    Kitajima, Yasuo
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (04) : 919 - 926
  • [10] Correlation of IgE autoantibody to BP180 with a severe form of bullous pemphigoid
    Iwata, Yohei
    Komura, Kazuhiro
    Kodera, Masanari
    Usuda, Toshikazu
    Yokoyama, Yoko
    Hara, Toshihide
    Muroi, Eiji
    Ogawa, Fumihide
    Takenaka, Motoi
    Sato, Shinichi
    [J]. ARCHIVES OF DERMATOLOGY, 2008, 144 (01) : 41 - 48