Celiac disease: role of intestinal compartments in the mucosal immune response
详细信息    查看全文
  • 作者:Giuseppe Iacomino ; Angela Marano ; Ilaria Stillitano…
  • 关键词:Celiac disease ; Intestinal compartments ; Cytokines ; Innate immunity ; Adaptive immunity ; Laser capture microdissection
  • 刊名:Molecular and Cellular Biochemistry
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:411
  • 期:1-2
  • 页码:341-349
  • 全文大小:822 KB
  • 参考文献:1.Maiuri L, Ciacci C, Ricciardelli I, Vacca L, Vacca L, Raia V, Auricchio S, Picard J, Osman M, Quaratino S, Londei M (2003) Association between innate response to gliadin and activation of pathogenic T cells in coeliac disease. Lancet 362:30–37CrossRef PubMed
    2.Brottveit M, Beitnes AC, Tollefsen S, Bratlie JE, Jahnsen FL, Johansen FE, Sollid LM, Lundin KE (2013) Mucosal cytokine response after short-term gluten challenge in celiac disease and non-celiac gluten sensitivity. Am J Gastroenterol 108(5):842–850CrossRef PubMed
    3.Koning F, Schuppan D, Cerf-Bensussan N, Sollid LM (2005) Pathomechanisms in celiac disease. Best Pract Res Clin Gastroenterol 19:373–387CrossRef PubMed
    4.Nilsen EM, Jahnsen FL, Lundin KE, Johansen FE, Fausa O, Sollid LM, Jahnsen J, Scott H, Brandtzaeg P (1998) Gluten induces an intestinal cytokine response strongly dominated by interferon gamma in patients with celiac disease. Gastroenterology 115:551–563CrossRef PubMed
    5.Troncone R, Gianfrani C, Mazzarella G, Greco L, Guardiola J, Auricchio S, De Berardinis P (1998) Majority of gliadin-specific T-cell clones from celiac small intestinal mucosa produce interferon-gamma and interleukin-4. Dig Dis Sci 43(1):156–161CrossRef PubMed
    6.Lahat N, Shapiro S, Karban A, Gerstein R, Kinarty A, Lerner A (1999) Cytokine profile in coeliac disease. Scand J Immunol 49(4):441–446CrossRef PubMed
    7.Forsberg G, Hernell O, Melgar S, Israelsson A, Hammarström S, Hammarström ML (2002) Paradoxical coexpression of proinflamatory and down-regulatory cytokines in intestinal T cells in childhood celiac disease. Gastroenterology 123(3):667–678CrossRef PubMed
    8.Di Sabatino A, Ciccocioppo R, Cupelli F, Cinque B, Millimaggi D, Clarkson MM, Paulli M, Cifone MG, Corazza GR (2006) Epithelium derived interleukin 15 regulates intraepithelial lymphocyte Th1 cytokine production, cytotoxicity, and survival in coeliac disease. Gut 55(4):469–477PubMedCentral CrossRef PubMed
    9.Fosberg G, Hernell O, Hammarström S, Hammarström ML (2007) Concomitant increase of IL-10 and pro-inflammatory cytokines in intraepithelial lymphocyte subsets in celiac disease. Int Immunol 19(8):993–1001CrossRef
    10.Simone NL, Bonner RF, Gillespie Emmert-Buck MR, Liotta LA (1998) Laser-capture microdissection: opening the microscopic frontier to molecular analysis. Trends Genet 14(7):272–276CrossRef PubMed
    11.Curran S, McKay JA, McLeod HL, Murray GI (2000) Laser-capture microscopy. Mol Pathol 53(2):64–68PubMedCentral CrossRef PubMed
    12.Lawrie LC, Curran S (2005) Laser-capture microdissection and colorectal cancer proteomics. Methods Mol Biol 293:245–253PubMed
    13.Yen TH, Wright NA (2006) The gastrointestinal tract stem cell niche. Stem Cell Rev 2(3):203–212CrossRef PubMed
    14.Hüe S, Mention JJ, Monteiro RC, Zhang S, Cellier C, Schmitz J, Verkarre V, Fodil N, Bahram S, Cerf-Bensussan N, Caillat-Zucman S (2004) A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease. Immunity 21:367–377CrossRef PubMed
    15.Monteleone G, Pender SL, Alstead E, Hauer AC, Lionetti P, McKenzie C, MacDonald TT (2001) Role of interferon alpha in promoting T helper cell type 1 responses in the small intestine in coeliac disease. Gut 48(3):425–429PubMedCentral CrossRef PubMed
    16.Weissmann C, Nagata S, Boll W, Fountoulakis M, Fujisawa A, Fujisawa JI, Haynes J, Henco K, Mantei N, Ragg H, Schein C, Schmid J, Shaw G, Streuli M, Taira H, Todokoro K, Weidle U (1094) Structure and expression of human IFN-alpha genes. Philos Trans R Soc Lond B Biol Sci 24(299):7–28
    17.Feldman E, Ahmed T, Lutton JD, Farley T, Tani K, Freund M, Asano S, Abraham NG (1997) Adenovirus mediated alpha interferon (IFN-alpha) gene transfer into CD34 + cells and CML mononuclear cells. Stem Cells 15(5):386–395CrossRef PubMed
    18.Airò P, Ghidini C, Zanotti C, Scarsi M, Cattaneo R, Caimi L, Imberti L (2008) Upregulation of myxovirus-resistance protein A: a possible marker of type I interferon induction in systemic sclerosis. Rheumatology 35(11):2192–2200CrossRef
    19.van der Voort LF, Vennegoor A, Visser A, Knol DL, Uitdehaag BM, Barkhof F, Oudejans CB, Polman CH, Killestein J (2010) Spontaneous MxA mRNA level predicts relapses in patients with recently diagnosed MS. Neurology 75(14):1228–1233
    20.Maiuri L, Ciacci C, Auricchio S, Brown V, Quaratino S, Londei M (2000) Interleukin 15 mediates epithelial changes in celiac disease. Gastroenterology 119:996–1006CrossRef PubMed
    21.Mention JJ, Ben Ahmed M, Begue B, Barbe U, Verkarre V, Asnafi V, Colombel JF, Cugnenc PH, Ruemmele FM, McIntyre E, Brousse N, Cellier C, Cerf-Bensussan N (2003) Interleukin 15: a key to disrupted intraepithelial lymphocyte homeostasis and lymphomagenesis in celiac disease. Gastroenterology 125:730–745CrossRef PubMed
    22.Bernardo D, Garrote JA, Allegretti Y, León A, Gómez E, Bermejo-Martin JF, Calvo C, Riestra S, Fernández-Salazar L, Blanco-Quirós A, Chirdo F, Arranz E (2008) Higher constitutive IL15Ra expression and lower IL-15 response threshold in coeliac disease patients. Clin Exp Immunol 154(1):64–73PubMedCentral CrossRef PubMed
    23.Monteleone G, Pender SL, Wathen NC, MacDonald TT (2001) Interferon-alphadrives T cell-mediated immunopathology in the intestine. Eur J Immunol 31:2247–2255CrossRef PubMed
    24.Fernandez S, Molina IJ, Romero P, González R, Peña J, Sánchez F, Reynoso FR, Pérez-Navero JL, Estevez O, Ortega C, Santamaría M (2011) Characterization of gliadin-specific Th17 cells from the mucosa of celiac disease patients. Am J Gastroenterol 106:528–538CrossRef PubMed
    25.Fina D, Sarra M, Caruso R, Del Vecchio Blanco G, Pallone F, MacDonald TT, Monteleone G (2008) Interleukin 21 contributes to the mucosal T helper cell type 1 response in coeliac disease. Gut 57(7):887–892CrossRef PubMed
    26.Bodd M, Ráki M, Tollefsen S, Fallang LE, Bergseng E, Lundin KE, Sollid LM (2010) HLA-DQ2-restricted gluten-reactive T cells produce IL-21 but not IL-17 or IL-22. Mucosal Immunol 3(6):594–601CrossRef PubMed
    27.Sapone A, Lammers KM, Mazzarella G, Mikhailenko I, Cartenì M, Casolaro V, Fasano A (2010) Differential mucosal IL-17 expression in two gliadin-induced disorders: gluten sensitivity and the autoimmune enteropathy celiac disease. Int Arch Allergy Immunol 152(1):75–80PubMedCentral CrossRef PubMed
    28.Monteleone I, Sarra M, Del Vecchio Blanco G, Paoluzi OA, Franzè E, Fina D, Fabrizi A, MacDonald TT, Pallone F, Monteleone G (2010) Characterization of IL-17A-producing cells in celiac disease mucosa. J Immunol 184(4):2211–2218CrossRef PubMed
    29.Lahdenperä AI, Hölttä V, Ruohtula T, Salo HM, Orivuori L, Westerholm-Ormio M, Savilahti E, Fälth-Magnusson K, Högberg L, Ludvigsson J, Vaarala O (2012) Up-regulation of small intestinal interleukin-17 immunity in untreated coeliac disease but not in potential coeliac disease or in type 1 diabetes. Clin Exp Immunol 167(2):226–234PubMedCentral CrossRef PubMed
    30.Lahat N, Shapiro S, Karban R, Gerstein R, Kinarty A, Lerner A (1999) Cytokine profile in coeliac disease. Scand J Immunol 49:441–446CrossRef PubMed
    31.Hansson T, Ulfgren AK, Lindroos E, DannAEus A, Dahlbom I, Klareskog L (2002) Transforming growth factor-beta (TGF-beta) and tissue transglutaminase expression in the small intestine in children with coeliac disease. Scand J Immunol 56(5):530–537CrossRef PubMed
    32.Salvati V, Mazzarella G, Gianfrani C, Levings MK, Stefanile R, De Giulio B, Iaquinto G, Giardullo N, Auricchio S, Roncarolo MG, Troncone R (2005) Recombinant human IL-10 suppresses gliadindependent T-cell activation in ex vivo cultured celiac intestinal mucosa. Gut 54:46–53PubMedCentral CrossRef PubMed
    33.Forsberg G, Hernell O, Melgar S, Israelsson A, Hammarström S, Hammarström ML (2002) Paradoxical coexpression of proinflammatory and down-regulatory cytokines in intestinal T-cells in childhood celiac disease. Gastroenterology 123:667–678CrossRef PubMed
    34.Gianfrani C, Leving M, Sartirana C, Mazzarella G, Barba G, Zanzi D, Camarca A, Iaquinto G, Giardullo N, Auricchio S, Troncone R, Roncarolo MG (2006) Gliadin-specific type-1 regulatory T-cells from intestinal mucosa of treated celiac patients inhibit pathogenic T-cells. J Immunol 177:4178–4186CrossRef PubMed
  • 作者单位:Giuseppe Iacomino (1)
    Angela Marano (1)
    Ilaria Stillitano (1)
    Vera Rotondi Aufiero (1)
    Gaetano Iaquinto (2)
    Michele Schettino (3)
    Armando Masucci (4)
    Riccardo Troncone (5) (6)
    Salvatore Auricchio (5) (6)
    Giuseppe Mazzarella (1) (6)

    1. Institute of Food Sciences, CNR, via Roma 64, 83100, Avellino, Italy
    2. Gastroenterology and Digestive Endoscopy Service, S. Rita Clinic, via Appia, 83042, Atripalda, Italy
    3. Gastroenterology and Digestive Endoscopy Service, San G. Moscati Hospital, Contrada Amoretta, 83100, Avellino, Italy
    4. Department of Preventive Medicine San G. Moscati Hospital, Contrada Amoretta, 83100, Avellino, Italy
    5. Department of Translational Medicine-Pediatric Section, University of Naples “Federico II”, Naples, Italy
    6. European Laboratory for the Investigation of Food-Induced Disease (ELFID), University of Naples “Federico II”, via Pansini, 80131, Naples, Italy
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Biochemistry
    Medical Biochemistry
    Oncology
    Cardiology
  • 出版者:Springer Netherlands
  • ISSN:1573-4919
文摘
Different approaches have been used to study the pattern of cytokines in celiac disease (CD). Laser capture microdissection (LCM) is a powerful tool for the isolation of specific tissue compartments. We aimed to investigate the mucosal immune response that takes place in different intestinal compartments of CD patients, dissected by LCM, analyzing cytokine expression profile. Frozen section of jejunum was obtained from 15 untreated CD and 15 control. Surface epithelium and lamina propria compartment were isolated by LCM. RNA from each LCM sample was extracted and, after a retrotranscription step, messenger RNA levels for MxA, IL-15, TNF-α, IFN-γ, IL-17α, IL-21, IL-10, and TGF-β were determined by quantitative reverse transcriptase-PCR. Increased gene expression levels of MxA, IL-15, TNF-α, IL-10, and TGF-β was observed in the surface epithelium of untreated CD with respect to control. Furthermore, all the cytokines investigated were upregulated in the lamina propria of untreated CD as compared to control. Within the untreated CD group the expression of IL-15 was higher, in the surface epithelium than in the lamina propria, whereas the expression levels of IL-17 and IL-21 were higher in the lamina propria than in the surface epithelium. Finally, high levels of IL-10 and TGF-β were detected in both compartments of untreated CD biopsies. In CD, surface epithelium and lamina propria compartments, play a prominent role in determining innate and adaptive immunity, respectively. Conversely, surface epithelium and lamina propria produce high levels of anti-inflammatory cytokines, suggesting that both compartments are involved in the immunoregulatory response. Keywords Celiac disease Intestinal compartments Cytokines Innate immunity Adaptive immunity Laser capture microdissection

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700