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Volumn 178, Issue , 2000, Pages 13-20

Gene therapy of severe combined immunodeficiencies

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE DEAMINASE;

EID: 0034511449     PISSN: 01052896     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-065X.2000.17806.x     Document Type: Review
Times cited : (21)

References (60)
  • 1
    • 0025182977 scopus 로고
    • European experience of bone-marrow transplantation for severe combined immunodeficiency
    • (1990) Lancet , vol.336 , pp. 850-854
    • Fischer, A.1
  • 2
    • 0033580206 scopus 로고    scopus 로고
    • Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency
    • (1999) N Engl J Med , vol.340 , pp. 508-516
    • Buckley, R.H.1
  • 4
    • 0027939098 scopus 로고
    • Relationship between patterns of engraftment in peripheral blood and immune reconstitution after allogeneic bone marrow transplantation for (severe) combined immunodeficiency
    • (1994) Blood , vol.84 , pp. 3936-3947
    • Van Leeuwen, J.E.1
  • 6
    • 0032833976 scopus 로고    scopus 로고
    • Long-term chimerism and B-cell function after bone marrow transplantation in patients with severe combined immunodeficiency with B cells: A single-center study of 22 patients
    • (1999) Blood , vol.94 , pp. 2923-2930
    • Haddad, E.1
  • 10
    • 0029962080 scopus 로고    scopus 로고
    • The interleukin-2 receptor gamma chain: Its role in the multiple cytokine receptor complexes and T cell development in XSCID
    • (1996) Annu Rev Immunol , vol.14 , pp. 179-205
    • Sugamura, K.1
  • 11
    • 0027403374 scopus 로고
    • Interleukin-2 receptor γ-chain mutation results in X-linked severe combined immunodeficiency in humans
    • (1993) Cell , vol.73 , pp. 147-157
    • Noguchi, M.1    Yi, H.2
  • 12
    • 0029924265 scopus 로고    scopus 로고
    • The molecular basis of X-linked severe combined immunodeficiency: Defective cytokine receptor signaling
    • (1996) Annu Rev Med , vol.47 , pp. 229-239
    • Leonard, W.J.1
  • 13
    • 10544244162 scopus 로고    scopus 로고
    • Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells
    • (1996) N Engl J Med , vol.335 , pp. 1563-1567
    • Stephan, V.1
  • 14
    • 12944284582 scopus 로고    scopus 로고
    • Diversity, functionality, and stability of the T cell repertoire derived in vivo from a single human T cell precursor
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 274-278
    • Bousso, P.1
  • 16
    • 15844426339 scopus 로고    scopus 로고
    • c gene transfer into SCID X1 patients' B-cell lines restores normal high-affinity interleukin-2 receptor expression and function
    • (1996) Blood , vol.87 , pp. 3108-3116
    • Hacein-Bey, H.1
  • 20
    • 0029850719 scopus 로고    scopus 로고
    • Role of interleukin-2 (IL-2), IL-7, and IL-15 in natural killer cell differentiation from cord blood hematopoietic progenitor cells and from γc transduced severe combined immunodeficiency X1 bone marrow cells
    • (1996) Blood , vol.88 , pp. 3901-3909
    • Cavazzana-Calvo, M.1
  • 23
    • 0030796576 scopus 로고    scopus 로고
    • Full immunologic reconstitution following nonconditioned bone marrow transplantation for canine X-linked severe combined immunodeficiency
    • (1997) Blood , vol.90 , pp. 3214-3221
    • Felsburg, P.J.1
  • 24
    • 0028180218 scopus 로고
    • Organization of the human CD40L gene: Implications for molecular defects in X chromosome-linked hyper-IgM syndrome and prenatal diagnosis
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 2110-2114
    • Villa, A.1
  • 25
    • 0033229710 scopus 로고    scopus 로고
    • Restoration of lymphoid populations in a murine model of X-linked severe combined immunodeficiency by a gene-therapy approach
    • (1999) Blood , vol.94 , pp. 3027-3036
    • Lo, M.1
  • 26
    • 0034657369 scopus 로고    scopus 로고
    • Stable and functional lymphoid reconstitution common cytokine receptor γ chain deficient mice by retroviral-mediated gene transfer
    • (2000) Blood , vol.95 , pp. 3071-3077
    • Soudais, C.1
  • 30
    • 0034724857 scopus 로고    scopus 로고
    • Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease
    • (2000) Science , vol.288 , pp. 669-672
    • Cavazzana-Calvo, M.1
  • 31
    • 0031593688 scopus 로고    scopus 로고
    • + cells in ADA-deficient SCID neonates
    • (1998) Nat Med , vol.4 , pp. 775-780
    • Kohn, D.B.1
  • 33
    • 0029164841 scopus 로고
    • Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)
    • (1995) Nature , vol.377 , pp. 65-68
    • Macchi, P.1
  • 34
    • 0028857954 scopus 로고
    • Mutation of Jak3 in a patient with SCID: Essential role of Jak3 in lymphoid development
    • (1995) Science , vol.270 , pp. 797-800
    • Russell, S.M.1
  • 35
    • 0032188806 scopus 로고    scopus 로고
    • Role of JAK3 in CD40-mediated signaling
    • (1998) Blood , vol.92 , pp. 2435-2440
    • Jabara, H.H.1
  • 36
    • 10144253125 scopus 로고    scopus 로고
    • RAG mutations in human B cell-negative SCID
    • (1996) Science , vol.274 , pp. 97-99
    • Schwarz, K.1
  • 37
    • 0028864561 scopus 로고
    • Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency
    • (1995) Nat Med , vol.1 , pp. 1017-1023
    • Kohn, D.B.1
  • 38
    • 0028789792 scopus 로고
    • Gene therapy in peripheral blood lymphocytes and bone marrow for ADA-immunodeficient patients
    • (1995) Science , vol.270 , pp. 470-475
    • Bordignon, C.1
  • 39
    • 9244243165 scopus 로고    scopus 로고
    • Bone marrow gene transfer in three patients with adenosine deaminase deficiency
    • (1996) Gene Ther , vol.3 , pp. 179-183
    • Hoogerbrugge, P.M.1
  • 40
    • 0028340167 scopus 로고
    • ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency
    • (1994) Science , vol.264 , pp. 1599-1601
    • Chan, A.C.1
  • 41
    • 0028292001 scopus 로고
    • Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
    • (1994) Science , vol.264 , pp. 1596-1599
    • Elder, M.E.1
  • 44
    • 11944266638 scopus 로고
    • A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)
    • (1995) Genes Dev , vol.9 , pp. 1021-1032
    • Steimle, V.1
  • 45
    • 0031055891 scopus 로고    scopus 로고
    • RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency
    • (1997) EMBO J , vol.16 , pp. 1045-1055
    • Durand, B.1
  • 46
    • 0004419978 scopus 로고    scopus 로고
    • A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients
    • (1998) Nat Genet , vol.20 , pp. 273-277
    • Masternak, K.1
  • 53
    • 0032947284 scopus 로고    scopus 로고
    • Simultaneous infection with retroviruses pseudotyped with different envelope proteins bypasses viral receptor interference associated with colocalization of gp70 and target cells on fibronectin CH-296
    • (1999) J Virol , vol.73 , pp. 3960-3697
    • MacNeill, E.C.1
  • 56
    • 0029996147 scopus 로고    scopus 로고
    • In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
    • (1996) Science , vol.272 , pp. 263-267
    • Naldini, L.1
  • 58
    • 0031743608 scopus 로고    scopus 로고
    • Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery
    • (1998) J Virol , vol.72 , pp. 9873-9880
    • Zufferey, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.