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Pathogenesis of hypogammaglobulinaemia with thymoma and late-onset hypogammaglobulinaemia.

作者信息

Asherson G L, Johnson S, Platts-Mills T A, Webster A D

出版信息

J Clin Pathol Suppl (R Coll Pathol). 1979;13:5-9. doi: 10.1136/jcp.s3-13.1.5.

DOI:10.1136/jcp.s3-13.1.5
PMID:316437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1521585/
Abstract
摘要

相似文献

1
Pathogenesis of hypogammaglobulinaemia with thymoma and late-onset hypogammaglobulinaemia.伴胸腺瘤的低丙种球蛋白血症及迟发性低丙种球蛋白血症的发病机制
J Clin Pathol Suppl (R Coll Pathol). 1979;13:5-9. doi: 10.1136/jcp.s3-13.1.5.
2
Thymoma and hypogammaglobulinaemia with and without T suppressor cells.胸腺瘤与伴有或不伴有T抑制细胞的低丙种球蛋白血症
Clin Exp Immunol. 1984 Dec;58(3):619-24.
3
Imbalances of T-cells in thymoma-associated hypogammaglobulinaemia.胸腺瘤相关低丙种球蛋白血症中T细胞的失衡
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4
Suppressor T cells in the pathogenesis of hypogammaglobulinemia associated with a thymoma.与胸腺瘤相关的低丙种球蛋白血症发病机制中的抑制性T细胞
Trans Assoc Am Physicians. 1975;88:120-34.
5
Development of hypogammaglobulinaemia in a patient with common variable immunodeficiency.
Eur J Pediatr. 1989 Dec;149(3):175-6. doi: 10.1007/BF01958274.
6
Pre-B cell suppression by thymoma patient lymphocytes.胸腺瘤患者淋巴细胞对前B细胞的抑制作用。
Clin Exp Immunol. 1982 May;48(2):437-42.
7
T-cell abnormalities in antibody deficiency syndromes.抗体缺乏综合征中的T细胞异常。
Scand J Immunol. 1989 Oct;30(4):419-24. doi: 10.1111/j.1365-3083.1989.tb02445.x.
8
[Immune defect following thymoma. Case description and review].[胸腺瘤后的免疫缺陷。病例描述与综述]
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Mechanisms in secondary hypogammaglobulinaemia.继发性低丙种球蛋白血症的机制。
J Clin Pathol Suppl (R Coll Pathol). 1979;13:15-22. doi: 10.1136/jcp.s3-13.1.15.
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The role of suppressor cells in the pathogenesis of common variable hypogammaglobulinemia and the immunodeficiency associated with myeloma.抑制细胞在常见变异型低丙种球蛋白血症发病机制及与骨髓瘤相关免疫缺陷中的作用。
Fed Proc. 1976 Jul;35(9):2067-72.

引用本文的文献

1
Clinical and laboratory features of seventy-eight UK patients with Good's syndrome (thymoma and hypogammaglobulinaemia).78 例英国 Good 综合征（胸腺瘤和低丙种球蛋白血症）患者的临床和实验室特征。
Clin Exp Immunol. 2019 Jan;195(1):132-138. doi: 10.1111/cei.13216. Epub 2018 Oct 21.
2
Defective cellular immune response in vitro in common variable immunodeficiency.常见变异型免疫缺陷患者体外细胞免疫反应缺陷。
J Clin Immunol. 1981 Jan;1(1):65-72. doi: 10.1007/BF00915478.

本文引用的文献

1
A clinical and experimental study of agammaglobulinemia.无丙种球蛋白血症的临床与实验研究
J Lancet. 1955 Jun;75(6):245-71.
2
The spectrum of diseases associated with thymoma. Coincidence or syndrome?与胸腺瘤相关的疾病谱。是巧合还是综合征？
Arch Intern Med. 1974 Aug;134(2):374-9.
3
Identification and function of T cells in the peripheral blood of patients with hypogammaglobulinaemia.低丙种球蛋白血症患者外周血中T细胞的鉴定及功能
Clin Exp Immunol. 1974 Dec;18(4):499-504.
4
On the classification of patients with primary immunodeficiency disorders.关于原发性免疫缺陷病患者的分类
Clin Immunol Immunopathol. 1974 Nov;3(2):243-7. doi: 10.1016/0090-1229(74)90010-5.
5
Depression of immunological function in patients treated with phenytoin sodium (sodium diphenylhydantoin).接受苯妥英钠（二苯乙内酰脲钠）治疗患者的免疫功能抑制
Lancet. 1971 Dec 4;2(7736):1233-5. doi: 10.1016/s0140-6736(71)90547-2.
6
Reversible hypogammaglobulinaemia after diphenylhydantoin and hydroxyzine therapy.苯妥英钠和羟嗪治疗后可逆性低丙种球蛋白血症
Neth J Med. 1974;17(6):261-9.
7
Role of suppressor T cells in pathogenesis of common variable hypogammaglobulinaemia.抑制性T细胞在常见变异型低丙种球蛋白血症发病机制中的作用。
Lancet. 1974 Sep 14;2(7881):609-13. doi: 10.1016/s0140-6736(74)91940-0.
8
Reduced immunoglobulin concentration and impaired macrophage function in mice due to diphenylhydantoin.由于苯妥英钠，小鼠体内免疫球蛋白浓度降低且巨噬细胞功能受损。
Clin Exp Immunol. 1978 Sep;33(3):437-40.
9
Effect of peripheral blood lymphocytes from patients with aplastic anemia on granulocytic colony growth from HLA-matched and -mismatched marrows: effect of transfusion sensitization.
Blood. 1978 Jul;52(1):37-46.
10
B lymphocyte precursors in human bone marrow: an analysis of normal individuals and patients with antibody-deficiency states.
J Immunol. 1978 Apr;120(4):1169-75.