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Volumn 23, Issue 2, 2007, Pages 161-166

CD3 complex and immunodeficiencies;Anomalies d'expression du complexe récepteur T de l'antigène/CD3 et déficits immunitaires

Author keywords

[No Author keywords available]

Indexed keywords

CD3 ANTIGEN; CD4 ANTIGEN; CD8 ANTIGEN; T LYMPHOCYTE RECEPTOR ALPHA CHAIN; T LYMPHOCYTE RECEPTOR BETA CHAIN;

EID: 33847110642     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/2007232161     Document Type: Review
Times cited : (2)

References (33)
  • 1
    • 13144249155 scopus 로고    scopus 로고
    • Severe combined immunodeficiency. A model disease for molecular immunology and therapy
    • Fischer A, Le Deist F, Hacein-Bey-Abina S, et al. Severe combined immunodeficiency. A model disease for molecular immunology and therapy. Immunol Rev 2005 ; 203 : 98-109.
    • (2005) Immunol Rev , vol.203 , pp. 98-109
    • Fischer, A.1    Le Deist, F.2    Hacein-Bey-Abina, S.3
  • 2
    • 0000930996 scopus 로고    scopus 로고
    • Immunodeficiency disease due to deficiency of adenosine deaminase
    • Ochs HD, Smith CIE, Puck JM, eds, New York, Oxford University Press
    • Hirschhorn R. Immunodeficiency disease due to deficiency of adenosine deaminase. In: Ochs HD, Smith CIE, Puck JM, eds. Primary immunodeficiency diseases. A molecular and genetic approach. New York : Oxford University Press, 1999 : 121-39.
    • (1999) Primary immunodeficiency diseases. A molecular and genetic approach , pp. 121-139
    • Hirschhorn, R.1
  • 3
    • 0028183408 scopus 로고
    • The molecular basis of X-linked severe combined immunodeficiency: The role of the interleukin-2 receptor gamma chain as a common gamma chain, gamma c
    • Leonard WJ, Noguchi M, Russell SM, McBride OW. The molecular basis of X-linked severe combined immunodeficiency: the role of the interleukin-2 receptor gamma chain as a common gamma chain, gamma c. Immunol Rev 1994 ; 138 : 61-86.
    • (1994) Immunol Rev , vol.138 , pp. 61-86
    • Leonard, W.J.1    Noguchi, M.2    Russell, S.M.3    McBride, O.W.4
  • 4
    • 0029164841 scopus 로고
    • Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)
    • Macchi P, Villa A, Giliani S, et al. Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID). Nature 1995 ; 377 : 65-8.
    • (1995) Nature , vol.377 , pp. 65-68
    • Macchi, P.1    Villa, A.2    Giliani, S.3
  • 5
    • 0031740732 scopus 로고    scopus 로고
    • Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency
    • Puel A, Ziegler SF, Buckley RH, Leonard WJ. Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency. Nat Genet 1998 ; 20 : 394-7.
    • (1998) Nat Genet , vol.20 , pp. 394-397
    • Puel, A.1    Ziegler, S.F.2    Buckley, R.H.3    Leonard, W.J.4
  • 6
    • 10144253125 scopus 로고    scopus 로고
    • RAG mutations in human B cell-negative SCID
    • Schwarz K, Gauss GH, Ludwig L, et al. RAG mutations in human B cell-negative SCID. Science 1996 ; 274 : 97-9.
    • (1996) Science , vol.274 , pp. 97-99
    • Schwarz, K.1    Gauss, G.H.2    Ludwig, L.3
  • 7
    • 0035917489 scopus 로고    scopus 로고
    • Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency
    • Moshous D, Callebaut I, de Chasseval R, et al. Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency. Cell 2001 ; 105 : 177-86.
    • (2001) Cell , vol.105 , pp. 177-186
    • Moshous, D.1    Callebaut, I.2    de Chasseval, R.3
  • 8
    • 0034064779 scopus 로고    scopus 로고
    • Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease
    • Kung C, Pingel JT, Heikinheimo M, et al. Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease. Nat Med 2000 ; 6 : 343-5.
    • (2000) Nat Med , vol.6 , pp. 343-345
    • Kung, C.1    Pingel, J.T.2    Heikinheimo, M.3
  • 9
    • 0242285603 scopus 로고    scopus 로고
    • Effect of CD3delta deficiency on maturation of alpha/beta and gamma/delta T-cell lineages in severe combined immunodeficiency
    • Dadi HK, Simon AJ, Roifman CM. Effect of CD3delta deficiency on maturation of alpha/beta and gamma/delta T-cell lineages in severe combined immunodeficiency. N Engl J Med 2003 ; 349 : 1821-8.
    • (2003) N Engl J Med , vol.349 , pp. 1821-1828
    • Dadi, H.K.1    Simon, A.J.2    Roifman, C.M.3
  • 10
    • 14544288042 scopus 로고    scopus 로고
    • Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3
    • De Saint Basile G, Geissmann F, Flori E, et al. Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3. J Clin Invest 2004 ; 114 : 1512-7.
    • (2004) J Clin Invest , vol.114 , pp. 1512-1517
    • De Saint Basile, G.1    Geissmann, F.2    Flori, E.3
  • 11
    • 0036604916 scopus 로고    scopus 로고
    • The T-cell receptor signalosome: A dynamic structure with expanding complexity
    • Werlen G, Palmer E. The T-cell receptor signalosome: a dynamic structure with expanding complexity. Curr Opin Immunol 2002 ; 14 : 299-305.
    • (2002) Curr Opin Immunol , vol.14 , pp. 299-305
    • Werlen, G.1    Palmer, E.2
  • 12
    • 1842505447 scopus 로고    scopus 로고
    • Molecular mechanisms for the assembly of the T cell receptor-CD3 complex
    • Call ME, Wucherpfennig KW. Molecular mechanisms for the assembly of the T cell receptor-CD3 complex. Mol Immunol 2004 ; 40 : 1295-305.
    • (2004) Mol Immunol , vol.40 , pp. 1295-1305
    • Call, M.E.1    Wucherpfennig, K.W.2
  • 13
    • 0032037669 scopus 로고    scopus 로고
    • The CD3gamma chain is essential for development of both the TCRalphabeta and TCRgammadelta lineages
    • Haks MC, Krimpenfort P, Borst J, Kruisbeek AM. The CD3gamma chain is essential for development of both the TCRalphabeta and TCRgammadelta lineages. EMBO J 1998 ; 17 : 1871-82.
    • (1998) EMBO J , vol.17 , pp. 1871-1882
    • Haks, M.C.1    Krimpenfort, P.2    Borst, J.3    Kruisbeek, A.M.4
  • 14
    • 0030981412 scopus 로고    scopus 로고
    • CD3 delta deficiency arrests development of the alpha beta but not the gamma delta T cell lineage
    • Dave VP, Cao Z, Browne C, et al. CD3 delta deficiency arrests development of the alpha beta but not the gamma delta T cell lineage. EMBO J 1997 ; 16 : 1360-70.
    • (1997) EMBO J , vol.16 , pp. 1360-1370
    • Dave, V.P.1    Cao, Z.2    Browne, C.3
  • 15
    • 0027199532 scopus 로고
    • T cell development in mice that lack the zeta chain of the T cell antigen receptor complex
    • Love PE, Shores EW, Johnson MD, et al. T cell development in mice that lack the zeta chain of the T cell antigen receptor complex. Science 1993 ; 261 : 918-21.
    • (1993) Science , vol.261 , pp. 918-921
    • Love, P.E.1    Shores, E.W.2    Johnson, M.D.3
  • 16
    • 18044376405 scopus 로고    scopus 로고
    • Severe combined immunodeficiency caused by a splicing abnormality of the CD3delta gene
    • Takada H, Nomura A, Roifman CM, Hara T. Severe combined immunodeficiency caused by a splicing abnormality of the CD3delta gene. Eur J Pediatr 2005 ; 164 : 311-4.
    • (2005) Eur J Pediatr , vol.164 , pp. 311-314
    • Takada, H.1    Nomura, A.2    Roifman, C.M.3    Hara, T.4
  • 17
    • 0036092401 scopus 로고    scopus 로고
    • A study on CD45 isoform expression during T-cell development and selection events in the human thymus
    • Fukuhara K, Okumura M, Shiono H, et al. A study on CD45 isoform expression during T-cell development and selection events in the human thymus. Hum Immunol 2002 ; 63 : 394-404.
    • (2002) Hum Immunol , vol.63 , pp. 394-404
    • Fukuhara, K.1    Okumura, M.2    Shiono, H.3
  • 18
    • 0034720880 scopus 로고    scopus 로고
    • CD3delta couples T-cell receptor signalling to ERK activation and thymocyte positive selection
    • Delgado P, Fernandez E, Dave V, et al. CD3delta couples T-cell receptor signalling to ERK activation and thymocyte positive selection. Nature 2000 ; 406 : 426-30.
    • (2000) Nature , vol.406 , pp. 426-430
    • Delgado, P.1    Fernandez, E.2    Dave, V.3
  • 19
    • 0029094319 scopus 로고
    • Altered T cell development in mice with a targeted mutation of the CD3-epsilon gene
    • Malissen M, Gillet A, Ardouin L, et al. Altered T cell development in mice with a targeted mutation of the CD3-epsilon gene. EMBO J 1995 ; 14 : 4641-53.
    • (1995) EMBO J , vol.14 , pp. 4641-4653
    • Malissen, M.1    Gillet, A.2    Ardouin, L.3
  • 20
    • 0033623474 scopus 로고    scopus 로고
    • Function of CD3 epsilon-mediated signals in T cell development
    • Sommers CL, Dejarnette JB, Huang K, et al. Function of CD3 epsilon-mediated signals in T cell development. J Exp Med 2000 ; 192 : 913-19.
    • (2000) J Exp Med , vol.192 , pp. 913-919
    • Sommers, C.L.1    Dejarnette, J.B.2    Huang, K.3
  • 21
    • 0027509235 scopus 로고
    • Independent mutations of the human CD3-epsilon gene resulting in a T cell receptor/CD3 complex immunodeficiency
    • Soudais C, de Villartay JP, Le Deist F, et al. Independent mutations of the human CD3-epsilon gene resulting in a T cell receptor/CD3 complex immunodeficiency. Nat Genet 1993 ; 3 : 77-81.
    • (1993) Nat Genet , vol.3 , pp. 77-81
    • Soudais, C.1    de Villartay, J.P.2    Le Deist, F.3
  • 24
    • 0042344751 scopus 로고    scopus 로고
    • CD3γ chain deficiency leads to a cellular immunodeficiency with a mild clinical presentation
    • Van Tol M, Sanal O, Langlois Van den Bergh R, et al. CD3γ chain deficiency leads to a cellular immunodeficiency with a mild clinical presentation. Immmunologist 1997 ; (suppl 1): 41-3.
    • (1997) Immmunologist , Issue.SUPPL. 1 , pp. 41-43
    • Van Tol, M.1    Sanal, O.2    Langlois Van den Bergh, R.3
  • 25
    • 0037944038 scopus 로고    scopus 로고
    • TCR dynamics in human mature T lymphocytes lacking CD3 gamma
    • Torres PS, Alcover A, Zapata DA, et al. TCR dynamics in human mature T lymphocytes lacking CD3 gamma. J Immunol 2003 ; 170 : 5947-55.
    • (2003) J Immunol , vol.170 , pp. 5947-5955
    • Torres, P.S.1    Alcover, A.2    Zapata, D.A.3
  • 26
    • 33646378182 scopus 로고    scopus 로고
    • Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency
    • Rieux-Laucat F, Hivroz C, Lim A, et al. Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency. N Engl J Med 2006 ; 354 : 1913-21.
    • (2006) N Engl J Med , vol.354 , pp. 1913-1921
    • Rieux-Laucat, F.1    Hivroz, C.2    Lim, A.3
  • 27
    • 0027501806 scopus 로고
    • T cell development in mice lacking the CD3-zeta/eta gene
    • Malissen M, Gillet A, Rocha B, et al. T cell development in mice lacking the CD3-zeta/eta gene. EMBO J 1993 ; 12 : 4347-55.
    • (1993) EMBO J , vol.12 , pp. 4347-4355
    • Malissen, M.1    Gillet, A.2    Rocha, B.3
  • 28
    • 0031028629 scopus 로고    scopus 로고
    • -/- mice overtly react with self-major histocompatibility complex molecules upon restoration of normal surface density of T cell receptor-CD3 complex
    • -/- mice overtly react with self-major histocompatibility complex molecules upon restoration of normal surface density of T cell receptor-CD3 complex. J Exp Med 1997 ; 185 : 707-15.
    • (1997) J Exp Med , vol.185 , pp. 707-715
    • Lin, S.Y.1    Ardouin, L.2    Gillet, A.3
  • 29
    • 10544244162 scopus 로고    scopus 로고
    • Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells
    • Stephan V, Wahn V, Le Deist F, et al. Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells. N Engl J Med 1996 ; 335 : 1563-7.
    • (1996) N Engl J Med , vol.335 , pp. 1563-1567
    • Stephan, V.1    Wahn, V.2    Le Deist, F.3
  • 30
    • 0032528485 scopus 로고    scopus 로고
    • A case of Wiskott-Aldrich syndrome with dual mutations in exon 10 of the WASP gene: An additional de novo one-base insertion, which restores frame shift due to an inherent one-base deletion, detected in the major population of the patient's peripheral blood lymphocytes
    • Ariga T, Yamada M, Sakiyama Y, Tatsuzawa O. A case of Wiskott-Aldrich syndrome with dual mutations in exon 10 of the WASP gene: an additional de novo one-base insertion, which restores frame shift due to an inherent one-base deletion, detected in the major population of the patient's peripheral blood lymphocytes. Blood 1998 ; 92 : 699-701.
    • (1998) Blood , vol.92 , pp. 699-701
    • Ariga, T.1    Yamada, M.2    Sakiyama, Y.3    Tatsuzawa, O.4
  • 31
    • 24744460541 scopus 로고    scopus 로고
    • Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency
    • Wada T, Toma T, Okamoto H, et al. Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency. Blood 2005 ; 106 : 2099-101.
    • (2005) Blood , vol.106 , pp. 2099-2101
    • Wada, T.1    Toma, T.2    Okamoto, H.3
  • 32
    • 0029902033 scopus 로고    scopus 로고
    • Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency
    • Hirschhorn R, Yang DR, Puck JM, et al. Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency. Nat Genet 1996 ; 13 : 290-5.
    • (1996) Nat Genet , vol.13 , pp. 290-295
    • Hirschhorn, R.1    Yang, D.R.2    Puck, J.M.3
  • 33
    • 0028269436 scopus 로고
    • - thymic selection in humans lacking zap-70 kinase
    • - thymic selection in humans lacking zap-70 kinase. Cell 1994 ; 76 : 947-58.
    • (1994) Cell , vol.76 , pp. 947-958
    • Arpaia, E.1    Shahar, M.2    Dadi, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.