메뉴 건너뛰기




Volumn 15, Issue 1, 2016, Pages 67-73

Alterations in blood leukocytes of G551D-bearing cystic fibrosis patients undergoing treatment with ivacaftor

Author keywords

Blood; CFTR; G551D; Ivacaftor; Leukocyte; VX 770

Indexed keywords

CD11B ANTIGEN; CD16 ANTIGEN; CD63 ANTIGEN; CHEMOKINE RECEPTOR CXCR2; IVACAFTOR; AMINOPHENOL DERIVATIVE; CFTR PROTEIN, HUMAN; CHLORIDE CHANNEL STIMULATING AGENT; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; QUINOLONE DERIVATIVE;

EID: 84959557066     PISSN: 15691993     EISSN: 18735010     Source Type: Journal    
DOI: 10.1016/j.jcf.2015.02.010     Document Type: Article
Times cited : (42)

References (27)
  • 1
    • 0026523829 scopus 로고
    • Cystic fibrosis: molecular biology and therapeutic implications
    • Collins F.S. Cystic fibrosis: molecular biology and therapeutic implications. Science 1992, 256(5058):774-779.
    • (1992) Science , vol.256 , Issue.5058 , pp. 774-779
    • Collins, F.S.1
  • 2
    • 34447523813 scopus 로고    scopus 로고
    • Cystic fibrosis: lessons from the sweat gland
    • Quinton P.M. Cystic fibrosis: lessons from the sweat gland. Physiology (Bethesda) 2007, 22:212-225.
    • (2007) Physiology (Bethesda) , vol.22 , pp. 212-225
    • Quinton, P.M.1
  • 5
    • 84861780622 scopus 로고    scopus 로고
    • Immune responses in cystic fibrosis: are they intrinsically defective?
    • Ratner D., Mueller C. Immune responses in cystic fibrosis: are they intrinsically defective?. Am J Respir Cell Mol Biol 2012, 46(6):715-722.
    • (2012) Am J Respir Cell Mol Biol , vol.46 , Issue.6 , pp. 715-722
    • Ratner, D.1    Mueller, C.2
  • 8
    • 45949089501 scopus 로고    scopus 로고
    • A novel proteolytic cascade generates an extracellular matrix-derived chemoattractant in chronic neutrophilic inflammation
    • Gaggar A., Jackson P.L., Noerager B.D., O'Reilly P.J., McQuaid D.B., Rowe S.M., et al. A novel proteolytic cascade generates an extracellular matrix-derived chemoattractant in chronic neutrophilic inflammation. J Immunol 2008, 180(8):5662-5669.
    • (2008) J Immunol , vol.180 , Issue.8 , pp. 5662-5669
    • Gaggar, A.1    Jackson, P.L.2    Noerager, B.D.3    O'Reilly, P.J.4    McQuaid, D.B.5    Rowe, S.M.6
  • 9
    • 77956898288 scopus 로고    scopus 로고
    • Characterization of macrophage activation states in patients with cystic fibrosis
    • Murphy B.S., Bush H.M., Sundareshan V., Davis C., Hagadone J., Cory T.J., et al. Characterization of macrophage activation states in patients with cystic fibrosis. J Cyst Fibros 2010, 9(5):314-322.
    • (2010) J Cyst Fibros , vol.9 , Issue.5 , pp. 314-322
    • Murphy, B.S.1    Bush, H.M.2    Sundareshan, V.3    Davis, C.4    Hagadone, J.5    Cory, T.J.6
  • 10
    • 70350130097 scopus 로고    scopus 로고
    • Proteases and antiproteases in chronic neutrophilic lung disease - relevance to drug discovery
    • Greene C.M., McElvaney N.G. Proteases and antiproteases in chronic neutrophilic lung disease - relevance to drug discovery. Br J Pharmacol 2009, 158(4):1048-1058.
    • (2009) Br J Pharmacol , vol.158 , Issue.4 , pp. 1048-1058
    • Greene, C.M.1    McElvaney, N.G.2
  • 11
    • 84884545931 scopus 로고    scopus 로고
    • Ivacaftor treatment of cystic fibrosis patients with the G551D mutation: a review of the evidence
    • Kotha K., Clancy J.P. Ivacaftor treatment of cystic fibrosis patients with the G551D mutation: a review of the evidence. Ther Adv Respir Dis 2013, 7(5):288-296.
    • (2013) Ther Adv Respir Dis , vol.7 , Issue.5 , pp. 288-296
    • Kotha, K.1    Clancy, J.P.2
  • 12
    • 78549279173 scopus 로고    scopus 로고
    • Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation
    • Accurso F.J., Rowe S.M., Clancy J.P., Boyle M.P., Dunitz J.M., Durie P.R., et al. Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation. N Engl J Med 2010, 363(21):1991-2003.
    • (2010) N Engl J Med , vol.363 , Issue.21 , pp. 1991-2003
    • Accurso, F.J.1    Rowe, S.M.2    Clancy, J.P.3    Boyle, M.P.4    Dunitz, J.M.5    Durie, P.R.6
  • 13
    • 80455162465 scopus 로고    scopus 로고
    • A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
    • Ramsey B.W., Davies J., McElvaney N.G., Tullis E., Bell S.C., Drevinek P., et al. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J Med 2011, 365(18):1663-1672.
    • (2011) N Engl J Med , vol.365 , Issue.18 , pp. 1663-1672
    • Ramsey, B.W.1    Davies, J.2    McElvaney, N.G.3    Tullis, E.4    Bell, S.C.5    Drevinek, P.6
  • 14
    • 84959491541 scopus 로고    scopus 로고
    • Symposium session summaries
    • S36
    • Symposium session summaries. Pediatric pulmonology. 2013, 48:103-206. S36.
    • (2013) Pediatric pulmonology. , vol.48 , pp. 103-206
  • 15
    • 84879116310 scopus 로고    scopus 로고
    • Metabolic adaptation of neutrophils in cystic fibrosis airways involves distinct shifts in nutrient transporter expression
    • Laval J., Touhami J., Herzenberg L.A., Conrad C., Taylor N., Battini J.L., et al. Metabolic adaptation of neutrophils in cystic fibrosis airways involves distinct shifts in nutrient transporter expression. J Immunol 2013, 190(12):6043-6050.
    • (2013) J Immunol , vol.190 , Issue.12 , pp. 6043-6050
    • Laval, J.1    Touhami, J.2    Herzenberg, L.A.3    Conrad, C.4    Taylor, N.5    Battini, J.L.6
  • 16
    • 0026733319 scopus 로고
    • Differential up-regulation of specific and azurophilic granule membrane markers in electropermeabilized neutrophils
    • Niessen H.W., Verhoeven A.J. Differential up-regulation of specific and azurophilic granule membrane markers in electropermeabilized neutrophils. Cell Signal 1992, 4(5):501-509.
    • (1992) Cell Signal , vol.4 , Issue.5 , pp. 501-509
    • Niessen, H.W.1    Verhoeven, A.J.2
  • 17
    • 0027398448 scopus 로고
    • A subpopulation of Mac-1 (CD11b/CD18) molecules mediates neutrophil adhesion to ICAM-1 and fibrinogen
    • Diamond M.S., Springer T.A. A subpopulation of Mac-1 (CD11b/CD18) molecules mediates neutrophil adhesion to ICAM-1 and fibrinogen. J Cell Biol 1993, 120(2):545-556.
    • (1993) J Cell Biol , vol.120 , Issue.2 , pp. 545-556
    • Diamond, M.S.1    Springer, T.A.2
  • 18
    • 77950362382 scopus 로고    scopus 로고
    • The inflammasomes
    • Schroder K., Tschopp J. The inflammasomes. Cell 2010, 140(6):821-832.
    • (2010) Cell , vol.140 , Issue.6 , pp. 821-832
    • Schroder, K.1    Tschopp, J.2
  • 19
    • 1842331095 scopus 로고
    • Phorbol diester receptor copurifies with protein kinase C
    • Niedel J.E., Kuhn L.J., Vandenbark G.R. Phorbol diester receptor copurifies with protein kinase C. Proc Natl Acad Sci U S A 1983, 80(1):36-40.
    • (1983) Proc Natl Acad Sci U S A , vol.80 , Issue.1 , pp. 36-40
    • Niedel, J.E.1    Kuhn, L.J.2    Vandenbark, G.R.3
  • 20
    • 2642513984 scopus 로고    scopus 로고
    • On the mechanism and significance of ligand-induced internalization of human neutrophil chemokine receptors CXCR1 and CXCR2
    • Rose J.J., Foley J.F., Murphy P.M., Venkatesan S. On the mechanism and significance of ligand-induced internalization of human neutrophil chemokine receptors CXCR1 and CXCR2. J Biol Chem 2004, 279(23):24372-24386.
    • (2004) J Biol Chem , vol.279 , Issue.23 , pp. 24372-24386
    • Rose, J.J.1    Foley, J.F.2    Murphy, P.M.3    Venkatesan, S.4
  • 21
    • 0026660112 scopus 로고
    • The up- and down-modulation of immunoglobulin G Fc receptors and complement receptors on activated human neutrophils depends on the nature of activator
    • Leino L., Lilius E.M. The up- and down-modulation of immunoglobulin G Fc receptors and complement receptors on activated human neutrophils depends on the nature of activator. J Leukoc Biol 1992, 51(2):157-163.
    • (1992) J Leukoc Biol , vol.51 , Issue.2 , pp. 157-163
    • Leino, L.1    Lilius, E.M.2
  • 22
    • 84905992903 scopus 로고    scopus 로고
    • A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy
    • Pohl K., Hayes E., Keenan J., Henry M., Meleady P., Molloy K., et al. A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy. Blood 2014, 124(7):999-1009.
    • (2014) Blood , vol.124 , Issue.7 , pp. 999-1009
    • Pohl, K.1    Hayes, E.2    Keenan, J.3    Henry, M.4    Meleady, P.5    Molloy, K.6
  • 23
    • 0025949558 scopus 로고
    • Expression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin
    • Yoshimura K., Nakamura H., Trapnell B.C., Chu C.S., Dalemans W., Pavirani A., et al. Expression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin. Nucleic Acids Res 1991, 19(19):5417-5423.
    • (1991) Nucleic Acids Res , vol.19 , Issue.19 , pp. 5417-5423
    • Yoshimura, K.1    Nakamura, H.2    Trapnell, B.C.3    Chu, C.S.4    Dalemans, W.5    Pavirani, A.6
  • 24
    • 79956194922 scopus 로고    scopus 로고
    • Dysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa
    • Del Porto P., Cifani N., Guarnieri S., Di Domenico E.G., Mariggio M.A., Spadaro F., et al. Dysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa. PLoS One 2011, 6(5):e19970.
    • (2011) PLoS One , vol.6 , Issue.5 , pp. e19970
    • Del Porto, P.1    Cifani, N.2    Guarnieri, S.3    Di Domenico, E.G.4    Mariggio, M.A.5    Spadaro, F.6
  • 25
    • 79960641412 scopus 로고    scopus 로고
    • Defective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosis
    • Sorio C., Buffelli M., Angiari C., Ettorre M., Johansson J., Vezzalini M., et al. Defective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosis. PLoS One 2011, 6(7):e22212.
    • (2011) PLoS One , vol.6 , Issue.7 , pp. e22212
    • Sorio, C.1    Buffelli, M.2    Angiari, C.3    Ettorre, M.4    Johansson, J.5    Vezzalini, M.6
  • 27
    • 84859620802 scopus 로고    scopus 로고
    • Cystic fibrosis: a mucosal immunodeficiency syndrome
    • Cohen T.S., Prince A. Cystic fibrosis: a mucosal immunodeficiency syndrome. Nat Med 2012, 18(4):509-519.
    • (2012) Nat Med , vol.18 , Issue.4 , pp. 509-519
    • Cohen, T.S.1    Prince, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.