Treatment of Granulomas in Patients With Ataxia Telangiectasia

被引:23
作者
Woelke, Sandra [1 ]
Valesky, Eva [2 ]
Bakhtiar, Shahrzad [3 ]
Pommerening, Helena [1 ]
Pfeffermann, L. M. [3 ]
Schubert, Ralf [1 ]
Zielen, Stefan [1 ]
机构
[1] Goethe Univ, Dept Children & Adolescents, Div Allergol Pulmonol & Cyst Fibrosis, Frankfurt, Germany
[2] Goethe Univ, Dept Dermatol Venereol & Allergol, Frankfurt, Germany
[3] Goethe Univ, Dept Children & Adolescents, Div Stem Cell Transplantat & Immunol, Frankfurt, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
关键词
ataxia telangiectasia; granulomas; granulomatous inflammation; TNF inhibitors; primary immunodeficiency; COMMON VARIABLE IMMUNODEFICIENCY; CUTANEOUS GRANULOMAS; T-CELLS; DISEASE; INFLIXIMAB; DEFICIENCY; HOMEOSTASIS; INFECTIONS; REPERTOIRE; GENOTYPE;
D O I
10.3389/fimmu.2018.02000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by progressive cerebellar ataxia, growth retardation, immunodeficiency, chronic pulmonary disease and chromosomal instability. Cutaneous granulomas are a known phenomenon in A-T but extra-dermal manifestation of granulomas at bone and synovia has not been reported so far. The clinical presentation, immunological findings, the long-term course and treatment options of eight patients with severe granulomas will be reported. Methods: From our cohort of 44 classical A-T patients, eight patients aged 2-11 years (18.2%) presented with granulomas. Immunological features of patients with and without granulomas were compared. Five patients suffered from cutaneous manifestation, in two patients we detected a bone and in one a joint involvement. Patients with significant extra-dermal involvement as well as one patient with massive skin manifestation were treated with TNF inhibitors. The patient with granulomas at his finger joint and elbow was treated with hematopoietic stem cell transplantation (HSCT). Results: Interestingly, seven of eight patients with granulomas were total IgA deficient, but there were no differences in IgG and IgM levels. All lymphocytes subsets were equally distributed except patients with granuloma had significantly lower naive CD8 cells. In patients without treatment, four of eight showed a slow but significant enlargement of the granuloma. Treatment success with TNF inhibitors was variable. In one patient, treatment with TNF inhibitors led to a total remission for 3 years up to now. In two patients, treatment with TNF inhibitors led to a partial regression of granulomas. Treatment interruptions caused deterioration again. Conclusions: Granulomas in A-T progress slowly over years and can lead to significant morbidity. Treatment with TNF inhibitors was safe and in part successful in our patients. Interestingly HSCT leads to complete remission, and indicates that aberrant immune function is responsible for granulomas in A-T patients. AT A GLANCE COMMENTARY: Scientific knowledge on the subject: Little is known about the clinical presentation, course and treatment of granulomas in ataxia telangiectasia (A-T). In addition, this is the first report of extra-dermal manifestation of granulomas at bone and synovia in patients with A-T. What This Study Adds to the Field: Granulomas in A-T progress slowly over years and can lead to significant morbidity. Treatment with TNF inhibitors was safe and in part successful in our patients.
引用
收藏
页数:8
相关论文
共 47 条
  • [1] Potential target of infliximab in autoimmune and inflammatory diseases
    Atzeni, Fabiola
    Doria, Andrea
    Carrabba, Mario
    Turiel, Maurizio
    Sarzi-Puttini, Piercarlo
    [J]. AUTOIMMUNITY REVIEWS, 2007, 6 (08) : 529 - 536
  • [2] Live rubella virus vaccine long-term persistence as an antigenic trigger of cutaneous granulomas in patients with primary immunodeficiency
    Bodemer, C.
    Sauvage, V.
    Mahlaoui, N.
    Cheval, J.
    Couderc, T.
    Leclerc-Mercier, S.
    Debre, M.
    Pellier, I.
    Gagnieur, L.
    Fraitag, S.
    Fischer, A.
    Blanche, S.
    Lecuit, M.
    Eloit, M.
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2014, 20 (10) : O656 - O663
  • [3] BODER E, 1958, PEDIATRICS, V21, P526
  • [4] Cutaneous Granulomas in Ataxia Telangiectasia and Other Primary Immunodeficiencies: Reflection of Inappropriate Immune Regulation?
    Chiam, L. Y. T.
    Verhagen, M. M. M.
    Haraldsson, A.
    Wulffraat, N.
    Driessen, G. -J.
    Netea, M. G.
    Weemaes, C. M. R.
    Seyger, M. M. B.
    van Deuren, M.
    [J]. DERMATOLOGY, 2011, 223 (01) : 13 - 19
  • [5] Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects
    Chiriaco, Maria
    Salfa, Irene
    Di Matteo, Gigliola
    Rossi, Paolo
    Finocchi, Andrea
    [J]. PEDIATRIC ALLERGY AND IMMUNOLOGY, 2016, 27 (03) : 242 - 253
  • [6] Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B- and T-cell homeostasis and reduced immune repertoire diversity
    Driessen, Gertjan J.
    IJspeert, Hanna
    Weemaes, Corry M. R.
    Haraldsson, Asgeir
    Trip, Margreet
    Warris, Adilia
    van der Flier, Michiel
    Wulffraat, Nico
    Verhagen, Mijke M. M.
    Taylor, Malcolm A.
    van Zelm, Menno C.
    van Dongen, Jacques J. M.
    van Deuren, Marcel
    van der Burg, Mirjam
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 131 (05) : 1367 - U183
  • [7] Cutaneous granulomas as a presenting sign in ataxia-telangiectasia
    Drolet, BA
    Drolet, B
    Zvulunov, A
    Jacobsen, R
    Troy, J
    Esterly, NB
    [J]. DERMATOLOGY, 1997, 194 (03) : 273 - 275
  • [8] INFECTIONS ASSOCIATED WITH STREPTOCOCCUS CONSTELLATUS IN CHILDREN
    Faden, Howard
    Mohmand, Mustafa
    [J]. PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2017, 36 (11) : 1099 - 1100
  • [9] Fever of unknown origin in a patient with common variable immunodeficiency associated with multisystemic granulomatous disease
    Fernandez-Ruiz, Mario
    Guerra-Vales, Juan-Manuel
    Francisco-Javier, Castelbon-Fernandez
    Yolanda, Rodriguez-Gil
    Miguel-Angel, Martinez-Gonzalez
    Cristina, Garfia-Castillo
    Jesus, Ruiz-Contreras
    [J]. INTERNAL MEDICINE, 2007, 46 (15) : 1197 - 1201
  • [10] Infliximab for Treatment of Granulomatous Disease in Patients with Common Variable Immunodeficiency
    Franxman, Timothy J.
    Howe, Laura E.
    Baker, James R., Jr.
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 (07) : 820 - 827