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血友病患者的系列临床和免疫学异常情况。

Sequential clinical and immunologic abnormalities in hemophiliacs.

作者信息

Goldsmith J M, Kalish S B, Green D, Chmiel J S, Wallemark C B, Phair J P

出版信息

Arch Intern Med. 1985 Mar;145(3):431-4.

PMID:3919666
Abstract

We examined 35 patients with hemophilia to determine if there was an association between impaired cell-mediated immunity and the amount of factor concentrate use. There was a significant negative relationship between the logarithm of the helper-suppressor ratio and the logarithm of concentrate use determined over the previous one year, five years, and total lifetime. Similarly, the presence of splenomegaly was significantly associated with the logarithm of concentrate use for each time interval. Hypergammaglobulinemia, anergy, and lymphadenopathy were present in a high proportion of patients. Repeated study of 30 of these patients at eight to 14 months showed no significant changes in their T-cell subsets. At follow-up, 16 patients had lymphadenopathy with or without splenomegaly and four had splenomegaly alone. No significant associations between concentrate use during the study period and changes in T-cell subsets or clinical condition were found.

摘要

我们检查了35例血友病患者,以确定细胞介导免疫受损与凝血因子浓缩剂使用量之间是否存在关联。在前一年、五年和整个生命周期中,辅助性T细胞与抑制性T细胞比值的对数与凝血因子浓缩剂使用量的对数之间存在显著的负相关关系。同样,脾肿大的存在与每个时间间隔内凝血因子浓缩剂使用量的对数显著相关。高丙种球蛋白血症、无反应性和淋巴结病在很大一部分患者中存在。对其中30例患者在8至14个月时进行的重复研究显示,他们的T细胞亚群没有显著变化。随访时,16例患者有淋巴结病,伴或不伴脾肿大,4例患者仅有脾肿大。在研究期间,未发现凝血因子浓缩剂的使用与T细胞亚群变化或临床状况之间存在显著关联。

相似文献

1
Sequential clinical and immunologic abnormalities in hemophiliacs.血友病患者的系列临床和免疫学异常情况。
Arch Intern Med. 1985 Mar;145(3):431-4.
2
T-cell alterations in hemophiliacs treated with commercial clotting factor concentrates.接受商用凝血因子浓缩物治疗的血友病患者的T细胞改变。
Thromb Haemost. 1983 Aug 30;50(2):552-6.
3
Progressive change in lymphocyte distribution and degree of hypergammaglobulinemia with age in children with hemophilia.血友病患儿淋巴细胞分布及高丙种球蛋白血症程度随年龄的渐进性变化。
J Clin Immunol. 1986 Mar;6(2):121-9. doi: 10.1007/BF00918744.
4
The course of preexistent immune abnormalities in HIV negative haemophiliacs treated for two years with a monoclonal purified factor VIII concentrate.
Thromb Haemost. 1993 Apr 1;69(4):306-10.
5
[Lymphocyte subpopulations in hemophilia A and B].
Med Clin (Barc). 1984 Oct 20;83(12):479-81.
6
Humoral and cellular immune abnormalities in adult hemophiliacs followed over a 2-year period.
Diagn Clin Immunol. 1987;5(1):30-40.
7
Immunologic studies in asymptomatic hemophiliac patients.
Folia Haematol Int Mag Klin Morphol Blutforsch. 1986;113(5):708-15.
8
Abnormal T-cell subsets and mitogen responses in hemophiliacs exposed to factor concentrate.接触凝血因子浓缩物的血友病患者的T细胞亚群和丝裂原反应异常。
Am J Dis Child. 1984 Jul;138(7):645-8. doi: 10.1001/archpedi.1984.02140450027008.
9
Impaired cell-mediated immunity in patients with classic hemophilia.
N Engl J Med. 1983 Jan 13;308(2):79-83. doi: 10.1056/NEJM198301133080205.
10
Immunologic dysfunction in patients with classic hemophilia receiving lyophilized factor VIII concentrates and cryoprecipitate.接受冻干因子VIII浓缩物和冷沉淀的经典血友病患者的免疫功能障碍。
Can Med Assoc J. 1983 Oct 1;129(7):713-7.

引用本文的文献

1
Altered immunity in hemophilia correlates with the presence of antibody to human T-cell lymphotropic virus type III (HTLV-III).血友病患者免疫功能的改变与抗人类嗜T淋巴细胞病毒III型(HTLV-III)抗体的存在相关。
J Clin Immunol. 1986 Jan;6(1):37-42. doi: 10.1007/BF00915362.