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Treatment of lymphopenic hypogammaglobulinemia and bone-marrow aplasia by transplantation of allogeneic marrow. Crucial role of histocompatiility matching.

作者信息

Meuwissen H J, Gatti R A, Terasaki P I, Hong R, Good R A

出版信息

N Engl J Med. 1969 Sep 25;281(13):691-7. doi: 10.1056/NEJM196909252811302.

DOI:10.1056/NEJM196909252811302
PMID:4186068
Abstract
摘要

相似文献

1
Treatment of lymphopenic hypogammaglobulinemia and bone-marrow aplasia by transplantation of allogeneic marrow. Crucial role of histocompatiility matching.
N Engl J Med. 1969 Sep 25;281(13):691-7. doi: 10.1056/NEJM196909252811302.
2
Transplantation of bone-marrow cells and fetal thymus in an infant with lymphopenic immunological deficiency.对一名患有淋巴细胞减少性免疫缺陷的婴儿进行骨髓细胞和胎儿胸腺移植。
Lancet. 1969 Jun 21;1(7608):1223-7. doi: 10.1016/s0140-6736(69)92112-6.
3
Treatment of autosomal recessive lymphopenic agammaglobulinemia by transplantation of matched allogeneic bone marrow.通过移植匹配的异基因骨髓治疗常染色体隐性淋巴细胞减少性无丙种球蛋白血症。
Am J Med. 1973 Jan;54(1):98-110. doi: 10.1016/0002-9343(73)90088-0.
4
The problems and practice of bone marrow transplantation in man: the severe combined immunodeficiency syndrome as the ideal model.人类骨髓移植的问题与实践:以重症联合免疫缺陷综合征作为理想模型
Transplant Proc. 1972 Dec;4(4):565-6.
5
Immunological reconstitution of sex-linked lymphopenic immunological deficiency.性连锁淋巴细胞减少性免疫缺陷的免疫重建
Lancet. 1968 Dec 28;2(7583):1366-9. doi: 10.1016/s0140-6736(68)92673-1.
6
Thymic dysplasia.
J Pediatr. 1969 Aug;75(2):229-35. doi: 10.1016/s0022-3476(69)80393-8.
7
[Bone marrow transplantation. Immunological problems, current concepts and therapeutic indications].[骨髓移植。免疫问题、当前概念及治疗指征]
Ther Umsch. 1971 Sep;28(9):596-600.
8
Transplantation of HL-A identical allogeneic bone marrow to a patient with acute lymphocytic leukemia.将HL-A相同的同种异体骨髓移植给一名急性淋巴细胞白血病患者。
Blood. 1970 Dec;36(6):736-47.
9
Survival of group A erythrocytes following bone marrow transplantation for reconstruction of lymphopenic hypogammaglobulinemia.骨髓移植重建淋巴细胞减少性低丙种球蛋白血症后A组红细胞的存活情况。
Blood. 1971 Jul;38(1):60-5.
10
Heterogeneity of phenotypic expression in a family with Swiss-type agammaglobulinemia: observations on the acquisition of agammaglobulinemia.
J Pediatr. 1971 Jun;78(6):968-80. doi: 10.1016/s0022-3476(71)80426-2.

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Flt3L 治疗骨髓供者可增加移植物浆细胞样树突状细胞含量并改善同种异体移植结局。
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T-cell-replete haploidentical bone marrow transplantation for X-linked severe combined immunodeficiency.T细胞充足的单倍体相合骨髓移植治疗X连锁重症联合免疫缺陷病
Singapore Med J. 2020 May;61(5):284-285. doi: 10.11622/smedj.2018101. Epub 2018 Aug 21.
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Blood Res. 2015 Dec;50(4):194-203. doi: 10.5045/br.2015.50.4.194. Epub 2015 Dec 21.
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Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency.使用匹配的同胞供体和无关供体进行无化疗预处理的造血干细胞移植治疗重症联合免疫缺陷的疗效比较。
J Allergy Clin Immunol. 2014 Oct;134(4):935-943.e15. doi: 10.1016/j.jaci.2014.06.021. Epub 2014 Aug 7.
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Stem cell and tissue engineering in breast reconstruction.干细胞与组织工程在乳房重建中的应用
Gland Surg. 2014 Feb;3(1):55-61. doi: 10.3978/j.issn.2227-684X.2014.02.11.
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Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency.宿主自然杀伤细胞免疫是严重联合免疫缺陷患者供体细胞植入许可的关键指标。
J Allergy Clin Immunol. 2014 Jun;133(6):1660-6. doi: 10.1016/j.jaci.2014.02.042. Epub 2014 May 1.
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HLA matching and the point system.人类白细胞抗原匹配与评分系统。
Clin Transplant. 1993;7(4):353-356.