메뉴 건너뛰기




Volumn 96, Issue 1, 2011, Pages 13-15

In mixed hematopoietic chimerism, the donor red cells win

Author keywords

[No Author keywords available]

Indexed keywords

ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION; APOPTOSIS; CELL TYPE; CHIMERA; DONOR; EDITORIAL; ENGRAFTMENT; ERYTHROCYTE; ERYTHROID PRECURSOR CELL; ERYTHROPOIESIS; GRAFT FAILURE; HEMATOPOIESIS; HEMOGLOBINOPATHY; HOST CELL; LYMPHOCYTE SUBPOPULATION; RISK ASSESSMENT; SICKLE CELL ANEMIA; THALASSEMIA; TREATMENT RESPONSE;

EID: 78651107396     PISSN: 03906078     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.2010.035576     Document Type: Editorial
Times cited : (29)

References (18)
  • 3
    • 0033996420 scopus 로고    scopus 로고
    • Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation
    • Andreani M, Nesci S, Lucarelli G, Tonucci P, Rapa S, Angelucci E, et al. Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation. Bone Marrow Transplant. 2000;25(4):401-4.
    • (2000) Bone Marrow Transplant , vol.25 , Issue.4 , pp. 401-404
    • Andreani, M.1    Nesci, S.2    Lucarelli, G.3    Tonucci, P.4    Rapa, S.5    Angelucci, E.6
  • 5
    • 78650991791 scopus 로고    scopus 로고
    • Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease
    • Andreani M, Testi M, Gaziev J, Condello R, Bontadini A, Tazzari PL, et al. Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease. Haematologica 2011;96(1):128-33.
    • (2011) Haematologica , vol.96 , Issue.1 , pp. 128-133
    • Andreani, M.1    Testi, M.2    Gaziev, J.3    Condello, R.4    Bontadini, A.5    Tazzari, P.L.6
  • 6
    • 47749098306 scopus 로고    scopus 로고
    • Relationship between mixed chimerism and rejection after bone marrow transplantation in thalassaemia
    • Andreani M, Testi M, Battarra M, Indigeno P, Guagnano A, Polchi P, et al. Relationship between mixed chimerism and rejection after bone marrow transplantation in thalassaemia. Blood Transfus. 2008;6(3):143-9.
    • (2008) Blood Transfus , vol.6 , Issue.3 , pp. 143-149
    • Andreani, M.1    Testi, M.2    Battarra, M.3    Indigeno, P.4    Guagnano, A.5    Polchi, P.6
  • 7
    • 0033230960 scopus 로고    scopus 로고
    • Engraftment kinetics after nonmyeloablative allogeneic peripheral blood stem cell transplantation: Full donor T-cell chimerism precedes alloimmune responses
    • Childs R, Clave E, Contentin N, Jayasekera D, Hensel N, Leitman S, et al. Engraftment kinetics after nonmyeloablative allogeneic peripheral blood stem cell transplantation: full donor T-cell chimerism precedes alloimmune responses. Blood. 1999;94(9):3234-41.
    • (1999) Blood , vol.94 , Issue.9 , pp. 3234-3241
    • Childs, R.1    Clave, E.2    Contentin, N.3    Jayasekera, D.4    Hensel, N.5    Leitman, S.6
  • 8
    • 49349089573 scopus 로고    scopus 로고
    • Erythroid-lineage-specific engraftment in patients with severe hemoglobinopathy following allogeneic hematopoietic stem cell transplantation
    • Armistead PM, Mohseni M, Gerwin R, Walsh EC, Iravani M, Chahardouli B, et al. Erythroid-lineage-specific engraftment in patients with severe hemoglobinopathy following allogeneic hematopoietic stem cell transplantation. Exp Hematol. 2008;36(9):1205-15.
    • (2008) Exp Hematol , vol.36 , Issue.9 , pp. 1205-1215
    • Armistead, P.M.1    Mohseni, M.2    Gerwin, R.3    Walsh, E.C.4    Iravani, M.5    Chahardouli, B.6
  • 9
    • 0035874519 scopus 로고    scopus 로고
    • Functional requirements for phenotypic correction of murine beta-thalassemia: Implications for human gene therapy
    • Persons DA, Allay ER, Sabatino DE, Kelly P, Bodine DM, Nienhuis AW. Functional requirements for phenotypic correction of murine beta-thalassemia: implications for human gene therapy. Blood. 2001;97(10):3275-82.
    • (2001) Blood , vol.97 , Issue.10 , pp. 3275-3282
    • Persons, D.A.1    Allay, E.R.2    Sabatino, D.E.3    Kelly, P.4    Bodine, D.M.5    Nienhuis, A.W.6
  • 11
    • 27744469194 scopus 로고    scopus 로고
    • Evidence for ineffective erythropoiesis in severe sickle cell disease
    • Wu CJ, Krishnamurti L, Kutok JL, Biernacki M, Rogers S, Zhang W, et al. Evidence for ineffective erythropoiesis in severe sickle cell disease. Blood. 2005;106(10):3639-45.
    • (2005) Blood , vol.106 , Issue.10 , pp. 3639-3645
    • Wu, C.J.1    Krishnamurti, L.2    Kutok, J.L.3    Biernacki, M.4    Rogers, S.5    Zhang, W.6
  • 12
    • 0034307683 scopus 로고    scopus 로고
    • A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in thai patients with thalassemia
    • Pootrakul P, Sirankapracha P, Hemsorach S, Moungsub W, Kumbunlue R, Piangitjagum A, et al. A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in thai patients with thalassemia. Blood. 2000;96(7):2606-12.
    • (2000) Blood , vol.96 , Issue.7 , pp. 2606-2612
    • Pootrakul, P.1    Sirankapracha, P.2    Hemsorach, S.3    Moungsub, W.4    Kumbunlue, R.5    Piangitjagum, A.6
  • 13
    • 85047690518 scopus 로고    scopus 로고
    • Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia
    • Kong Y, Zhou S, Kihm AJ, Katein AM, Yu X, Gell DA, et al. Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia. J Clin Invest. 2004;114(10):1457-66.
    • (2004) J Clin Invest , vol.114 , Issue.10 , pp. 1457-1466
    • Kong, Y.1    Zhou, S.2    Kihm, A.J.3    Katein, A.M.4    Yu, X.5    Gell, D.A.6
  • 14
    • 0033566713 scopus 로고    scopus 로고
    • Altered hematopoiesis in murine sickle cell disease
    • Blouin MJ, De Paepe ME, Trudel M. Altered hematopoiesis in murine sickle cell disease. Blood. 1999;94(4):1451-9.
    • (1999) Blood , vol.94 , Issue.4 , pp. 1451-1459
    • Blouin, M.J.1    de Paepe, M.E.2    Trudel, M.3
  • 16
    • 0016838875 scopus 로고
    • Ultrastructural studies of the bone marrow in sickle cell anaemia. I. The structure of sickled erythrocytes and reticulocytes and their phagocytic destruction
    • Grasso JA, Sullivan AL, Sullivan LW. Ultrastructural studies of the bone marrow in sickle cell anaemia. I. The structure of sickled erythrocytes and reticulocytes and their phagocytic destruction. Br J Haematol. 1975;31(2):135-48.
    • (1975) Br J Haematol , vol.31 , Issue.2 , pp. 135-148
    • Grasso, J.A.1    Sullivan, A.L.2    Sullivan, L.W.3
  • 17
    • 77956928344 scopus 로고    scopus 로고
    • Transfusion independence and HMGA2 activation after gene therapy of human beta-thalassaemia
    • Cavazzana-Calvo M, Payen E, Negre O, Wang G, Hehir K, Fusil F, et al. Transfusion independence and HMGA2 activation after gene therapy of human beta-thalassaemia. Nature. 2010;467(7313):318-22.
    • (2010) Nature , vol.467 , Issue.7313 , pp. 318-322
    • Cavazzana-Calvo, M.1    Payen, E.2    Negre, O.3    Wang, G.4    Hehir, K.5    Fusil, F.6
  • 18
    • 57349083313 scopus 로고    scopus 로고
    • Donor/recipient mixed chimerism does not predict graft failure in children with beta-thalassemia given an allogeneic cord blood transplant from an HLA-identical sibling
    • Lisini D, Zecca M, Giorgiani G, Montagna D, Cristantielli R, Labirio M, et al. Donor/recipient mixed chimerism does not predict graft failure in children with beta-thalassemia given an allogeneic cord blood transplant from an HLA-identical sibling. Haematologica. 2008;93(12):1859-67.
    • (2008) Haematologica , vol.93 , Issue.12 , pp. 1859-1867
    • Lisini, D.1    Zecca, M.2    Giorgiani, G.3    Montagna, D.4    Cristantielli, R.5    Labirio, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.