HLA-identical sibling and haploidentical, T-cell-depleted bone marrow transplantation for immunodeficiency

被引：1
|
作者：
Fischer, A
机构：
[1] Hopital Necker-Enfants Malades, Inserm U429, 75743 Paris Cedex 15, 149, rue de Sevres
来源：
IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA | 1996年 / 16卷 / 02期
基金：
澳大利亚研究理事会;
关键词：
D O I：
10.1016/S0889-8561(05)70251-4
中图分类号：
R392 [医学免疫学];
学科分类号：
100102 ;
摘要：
Most primary immunodeficiencies consist of intrinsic defects of lymphocytic or phagocytic cell lineages. Therefore, replacement of genetically impaired hematopoietic stem cells by normal hematopoietic stem cells is a logical therapeutic approach. In this article, results of haploidentical, T-cell-depleted bone marrow transplantation are compared with results of HLA-identical bone marrow transplanation.
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收藏
页码：361 / +
页数：1
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