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1
Immunological abnormalities in thalassaemia major. I. A transfusion-related increase in circulating cytoplasmic immunoglobulin-positive cells.重型地中海贫血的免疫异常。I. 与输血相关的循环细胞质免疫球蛋白阳性细胞增多。
Clin Exp Immunol. 1985 Nov;62(2):397-404.
2
Abnormalities in the immune system of children with beta-thalassaemia major.重型β地中海贫血患儿免疫系统的异常。
Clin Exp Immunol. 1987 Jun;68(3):621-9.
3
Lymphoid cell sets and serum immunoglobulins in patients with thalassaemia intermedia: relationship to serum iron and splenectomy.中间型地中海贫血患者的淋巴细胞集落和血清免疫球蛋白:与血清铁及脾切除术的关系
Br J Haematol. 1980 Jul;45(3):405-16. doi: 10.1111/j.1365-2141.1980.tb07161.x.
4
Transfusion-related immunologic abnormalities in beta-thalassemia major.重型β地中海贫血中与输血相关的免疫异常。
Birth Defects Orig Artic Ser. 1987;23(5A):587-93.
5
Effects of the allogeneic stimulation on B cell function in thalassaemic polytransfused patients.
Boll Ist Sieroter Milan. 1987;66(4):316-23.
6
Severe combined immunodeficiency with B lymphocytes: in vitro correction of defective immunoglobulin production by addition of normal T lymphocytes.伴有B淋巴细胞的重症联合免疫缺陷:通过添加正常T淋巴细胞对有缺陷的免疫球蛋白产生进行体外纠正。
Clin Exp Immunol. 1976 Oct;26(1):1-10.
7
Immunological profile after splenectomy in children with beta-thalassaemia major.
Acta Haematol. 1987;78(4):243-8. doi: 10.1159/000205886.
8
Immune profile alterations in thalassaemic patients.
Boll Ist Sieroter Milan. 1983;62(6):524-30.
9
Disproportionate lymphoid cell subsets in thalassaemia major: the relative contributions of transfusion and splenectomy.
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10
Iron-related disturbances of cell-mediated immunity in multitransfused children with thalassemia major.重型地中海贫血多次输血患儿铁相关的细胞介导免疫紊乱
Clin Exp Immunol. 1987 Apr;68(1):138-45.

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1
Immune responses in beta-thalassaemia: heme oxygenase 1 reduces cytokine production and bactericidal activity of human leucocytes.β-地中海贫血症的免疫反应:血红素加氧酶 1 可降低人白细胞的细胞因子产生和杀菌活性。
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2
Serum immunoglobulin levels in splenectomized and non- splenectomized patients with major Beta-thalassemia.重型β地中海贫血患者脾切除和未脾切除患者的血清免疫球蛋白水平。
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Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications.地中海贫血症和血红蛋白病中的感染:关注治疗相关并发症。
Mediterr J Hematol Infect Dis. 2009 Dec 28;1(1):e2009028. doi: 10.4084/MJHID.2009.028.
4
Modulation of the defective natural killer activity seen in thalassaemia major with desferrioxamine and alpha-interferon.去铁胺和α-干扰素对重型地中海贫血中缺陷性自然杀伤细胞活性的调节作用。
Clin Exp Immunol. 1987 Nov;70(2):345-53.
5
Immune cell functions in iron overload.铁过载中的免疫细胞功能。
Clin Exp Immunol. 1989 Jan;75(1):1-6.
6
The development of primed/memory CD8+ lymphocytes in vitro and in rejecting kidneys after transplantation.初始/记忆性CD8 +淋巴细胞在体外的发育以及移植后排斥反应肾脏中的发育。
Clin Exp Immunol. 1990 Aug;81(2):225-31. doi: 10.1111/j.1365-2249.1990.tb03322.x.
7
Serum amyloid A protein concentration in bone marrow transplantation for beta thalassaemia.β地中海贫血骨髓移植中血清淀粉样蛋白A蛋白浓度
J Clin Pathol. 1992 Apr;45(4):348-51. doi: 10.1136/jcp.45.4.348.

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1
Chelation therapy in beta-thalassemia major. III. The role of splenectomy in achieving iron balance.重型β地中海贫血的螯合疗法。III. 脾切除术在实现铁平衡中的作用。
J Pediatr. 1981 Nov;99(5):695-9. doi: 10.1016/s0022-3476(81)80386-1.
2
Lymphoid cell sets and serum immunoglobulins in patients with thalassaemia intermedia: relationship to serum iron and splenectomy.中间型地中海贫血患者的淋巴细胞集落和血清免疫球蛋白:与血清铁及脾切除术的关系
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Serum immunoglobulins in homozygous beta-thalassemia.纯合子β地中海贫血中的血清免疫球蛋白
Acta Haematol. 1981;65(1):21-5. doi: 10.1159/000207144.
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Circulating immunoglobulin-secreting cells in rheumatoid arthritis.类风湿关节炎中的循环免疫球蛋白分泌细胞
Clin Immunol Immunopathol. 1983 Oct;29(1):29-34. doi: 10.1016/0090-1229(83)90004-1.
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Involvement of transferrin and transferrin receptors in human natural killer effector:target interaction.转铁蛋白及转铁蛋白受体在人类自然杀伤效应细胞与靶细胞相互作用中的作用
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Transferrin receptor induction in mitogen-stimulated human T lymphocytes is required for DNA synthesis and cell division and is regulated by interleukin 2.丝裂原刺激的人T淋巴细胞中转铁蛋白受体的诱导对于DNA合成和细胞分裂是必需的,并且受白细胞介素2调节。
Proc Natl Acad Sci U S A. 1983 Jun;80(11):3494-8. doi: 10.1073/pnas.80.11.3494.
7
Diminished helper/suppressor lymphocyte ratios and natural killer activity in recipients of repeated blood transfusions.反复输血受者体内辅助/抑制淋巴细胞比例降低及自然杀伤细胞活性降低。
Blood. 1984 Jul;64(1):308-10.
8
Spontaneous and Concanavalin A-induced suppressor activity in control and Hodgkin's disease patients.对照患者和霍奇金病患者的自发及伴刀豆球蛋白A诱导的抑制活性
Br J Cancer. 1984 Mar;49(3):349-56. doi: 10.1038/bjc.1984.55.
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Immunologic abnormalities in patients receiving multiple blood transfusions.
Ann Intern Med. 1984 Feb;100(2):173-7. doi: 10.7326/0003-4819-100-2-173.
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NK and T cell subsets regulate antibody production by human in vivo antigen-induced lymphoblastoid B cells.自然杀伤细胞和T细胞亚群可调节人体内由抗原诱导的淋巴母细胞样B细胞产生抗体的过程。
J Immunol. 1984 Feb;132(2):611-5.

重型地中海贫血的免疫异常。I. 与输血相关的循环细胞质免疫球蛋白阳性细胞增多。

Immunological abnormalities in thalassaemia major. I. A transfusion-related increase in circulating cytoplasmic immunoglobulin-positive cells.

作者信息

Akbar A N, Giardina P J, Hilgartner M W, Grady R W

出版信息

Clin Exp Immunol. 1985 Nov;62(2):397-404.

PMID:3878749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1577434/
Abstract

Multiply transfused patients with beta-thalassaemia major have elevated serum immunoglobulin levels and a transfusion-related increase in (T8+) T-suppressor cells. We report here that these patients also have a significantly increased (P less than 0.001) proportion of B-cells that contain cytoplasmic immunoglobulin when visualized immediately upon isolation. On the other hand, the same cell populations do not exhibit an increase in the proportion of immunoglobulin-secreting cells as measured by a reverse haemolytic plaque assay. These results, together with those of ongoing studies, suggest that the cells containing the cytoplasmic immunoglobulin are likely to be terminally differentiated B-cells which persist in the circulation. While the reason for this phenomenon is not yet known, we have found that the increase in these cells is transfusion-related.

摘要

多次输血的重型β地中海贫血患者血清免疫球蛋白水平升高,且与输血相关的(T8 +)T抑制细胞增多。我们在此报告,这些患者在分离后立即观察时,含有细胞质免疫球蛋白的B细胞比例也显著增加(P小于0.001)。另一方面,通过反向溶血空斑试验测定,相同细胞群体中分泌免疫球蛋白的细胞比例并未增加。这些结果以及正在进行的研究结果表明,含有细胞质免疫球蛋白的细胞可能是终末分化的B细胞,它们持续存在于循环中。虽然这种现象的原因尚不清楚,但我们发现这些细胞的增加与输血有关。