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Reversal of natural killer defect in a patient with Chédiak-Higashi syndrome after bone-marrow transplantation.

作者信息

Virelizier J L, Lagrue A, Durandy A, Arenzana F, Oury C, Griscelli C, Reinert P

出版信息

N Engl J Med. 1982 Apr 29;306(17):1055-6. doi: 10.1056/nejm198204293061718.

DOI:10.1056/nejm198204293061718
PMID:7038504
Abstract
摘要

相似文献

1
Reversal of natural killer defect in a patient with Chédiak-Higashi syndrome after bone-marrow transplantation.骨髓移植后一名患有切-东综合征患者自然杀伤细胞缺陷的逆转
N Engl J Med. 1982 Apr 29;306(17):1055-6. doi: 10.1056/nejm198204293061718.
2
Natural killer cell activity in a patient with Chédiak-Higashi syndrome submitted to bone marrow transplantation.接受骨髓移植的切-东综合征患者的自然杀伤细胞活性
Pediatr Hematol Oncol. 1995 Jul-Aug;12(4):399-402. doi: 10.3109/08880019509029591.
3
Bone marrow transplantation in a patient with Chédiak-Higashi Syndrome.一名患有切-东综合征患者的骨髓移植
Birth Defects Orig Artic Ser. 1983;19(3):333-4.
4
Chediak-Higashi syndrome: reversal of increased susceptibility to infection by bone marrow transplantation.
Blood. 1976 Apr;47(4):555-9.
5
Treatment of Chediak-Higashi syndrome by allogenic bone marrow transplantation: report of 10 cases.异基因骨髓移植治疗切-东综合征：10例报告
Blood. 1995 Jun 1;85(11):3328-33.
6
Chediak-Higashi syndrome natural killer cells: a protein kinase C defective activation/regulation defect?
Eur J Pediatr. 1996 Mar;155(3):254. doi: 10.1007/BF01953949.
7
Chédiak-Higashi syndrome: hematopoietic chimerism corrects genetic defect.
Bone Marrow Transplant. 2001 Jun;27(11):1211-3. doi: 10.1038/sj.bmt.1703058.
8
Deficiency of inducible suppressor cell activity in the Chediak-Higashi syndrome.切迪阿克-东综合征中诱导性抑制细胞活性的缺乏。
Am J Hematol. 1987 Sep;26(1):55-66. doi: 10.1002/ajh.2830260107.
9
Characterization of a murine model (beige) for a natural killer cell immunodeficiency in the Chediak-Higashi syndrome of man.人类切-东综合征中自然杀伤细胞免疫缺陷的小鼠模型（米色）的特征描述。
Prog Clin Biol Res. 1982;94:315-25.
10
[The accelerated phase of Chediak-Higashi syndrome].[切-东综合征的加速期]
Arch Fr Pediatr. 1989 Dec;46(10):733-6.

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Drosophila mauve mutants reveal a role of LYST homologs late in the maturation of phagosomes and autophagosomes.果蝇洋红突变体揭示了 LYST 同源物在吞噬体和自噬体成熟后期的作用。
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Genetic defects in Chediak-Higashi syndrome and the beige mouse.
切-东综合征和米色小鼠的基因缺陷。
J Clin Immunol. 1998 Mar;18(2):97-105. doi: 10.1023/a:1023247215374.
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Natural killer cells: artifact to reality: an odyssey in biology.自然杀伤细胞：从人为现象到真实存在：生物学中的一段历程
Cancer Metastasis Rev. 1983;2(4):323-36. doi: 10.1007/BF00048565.
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Epstein-Barr serology in immunodeficiencies: an attempt to correlate with immune abnormalities in Wiskott-Aldrich and Chediak-Higashi syndromes and ataxia telangiectasia.免疫缺陷中的爱泼斯坦-巴尔病毒血清学：试图与维斯科特-奥尔德里奇综合征、切迪阿克-希加希综合征和共济失调毛细血管扩张症中的免疫异常相关联。
Clin Exp Immunol. 1984 Feb;55(2):249-56.
6
Deficiency of NK activity of HNK-1+ cells after transplantation of fetal thymus and liver or haploidentical soybean agglutinin-treated marrow cells in two severe combined immunodeficiency patients.两名重症联合免疫缺陷患者在移植胎儿胸腺和肝脏或单倍体相同的经大豆凝集素处理的骨髓细胞后，HNK-1+细胞的自然杀伤活性缺乏。
Clin Exp Immunol. 1985 Sep;61(3):608-13.
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Absence of complement receptor type 3 and lymphocyte function antigen 1 causing deficient phagocyte and lymphocyte functions.缺乏3型补体受体和淋巴细胞功能相关抗原1导致吞噬细胞和淋巴细胞功能缺陷。
Eur J Pediatr. 1988 Oct;148(1):58-61. doi: 10.1007/BF00441816.
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Deficiency of the adhesive protein complex lymphocyte function antigen 1, complement receptor type 3, glycoprotein p150,95 in a girl with recurrent bacterial infections. Effects on phagocytic cells and lymphocyte functions.一名反复发生细菌感染女孩中黏附蛋白复合物淋巴细胞功能抗原1、3型补体受体、糖蛋白p150,95的缺陷。对吞噬细胞和淋巴细胞功能的影响。
J Clin Invest. 1985 Dec;76(6):2385-92. doi: 10.1172/JCI112251.
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Effects of interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) on the expression of LFA-1 in the moderate phenotype of leukocyte adhesion deficiency (LAD).γ-干扰素（IFN-γ）和肿瘤坏死因子-α（TNF-α）对白细胞黏附缺陷（LAD）中度表型中淋巴细胞功能相关抗原-1（LFA-1）表达的影响
J Clin Immunol. 1989 May;9(3):200-7. doi: 10.1007/BF00916815.
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Bone marrow transplantation (BMT) for the syndrome of pigmentary dilution and lymphohistiocytosis (Griscelli's syndrome).针对色素稀释和淋巴细胞组织细胞增多综合征（格里斯塞利综合征）的骨髓移植
J Clin Immunol. 1990 May;10(3):146-53. doi: 10.1007/BF00917914.