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脾切除术后循环白细胞群体的持续变化。

Persistent changes in circulating white blood cell populations after splenectomy.

作者信息

Rab Minke A E, Meerveld-Eggink Aafke, van Velzen-Blad Heleen, van Loon Douwe, Rijkers Ger T, de Weerdt Okke

机构信息

Department of Internal Medicine, St. Antonius Hospital, Nieuwegein, The Netherlands.

Department of Internal Medicine and Dermatology, University Medical Centre Utrecht, Van Creveldkliniek, Heidelberglaan 100, 3508 GA, Utrecht, The Netherlands.

出版信息

Int J Hematol. 2018 Feb;107(2):157-165. doi: 10.1007/s12185-017-2335-9. Epub 2017 Sep 26.

DOI:10.1007/s12185-017-2335-9
PMID:28952075
Abstract

The effect of splenectomy on the incidence of infections and thromboembolisms has been investigated thoroughly. Nevertheless, the long-term effects of splenectomy on immunological profile and circulating blood counts have not been described before. To study such long-term effects, we analysed several parameters in splenectomised trauma patients and compared the results of this group ("otherwise healthy patients") to patients with a specific underlying disease. We measured platelet count, leukocytes and differential, lymphocyte subsets, serum levels of immunoglobulins, and complement pathways in 113 patients. Indications to perform a splenectomy were trauma (n = 42), Hodgkin lymphoma (n = 24), hereditary spherocytosis (n = 21), and immune thrombocytopenia (n = 26). In trauma patients lymphocytes and lymphocytes subsets were particularly elevated compared to normal population values. Splenectomised patients with Hodgkin lymphoma had significant lower numbers of T lymphocytes than trauma patients. Significant increases in platelets, leukocytes, and monocytes were observed in patients with hereditary spherocytosis. Occurrence of MBL genotype was different in ITP patients than in other splenectomised groups and the normal population. In splenectomised patients (> 4 years), platelet counts and lymphocyte subsets are increased which persist over time. As a result, these blood counts in splenectomised patients differ from reference values in the normal population.

摘要

脾切除术对感染和血栓栓塞发生率的影响已得到充分研究。然而,脾切除术对免疫特征和循环血细胞计数的长期影响此前尚未见报道。为研究此类长期影响,我们分析了脾切除术后创伤患者的几个参数,并将该组患者(“其他健康患者”)的结果与患有特定基础疾病的患者进行了比较。我们测量了113例患者的血小板计数、白细胞及其分类、淋巴细胞亚群、免疫球蛋白血清水平和补体途径。进行脾切除术的指征包括创伤(n = 42)、霍奇金淋巴瘤(n = 24)、遗传性球形红细胞增多症(n = 21)和免疫性血小板减少症(n = 26)。与正常人群值相比,创伤患者的淋巴细胞和淋巴细胞亚群尤其升高。霍奇金淋巴瘤脾切除患者的T淋巴细胞数量明显低于创伤患者。遗传性球形红细胞增多症患者的血小板、白细胞和单核细胞显著增加。免疫性血小板减少症患者的MBL基因型发生率与其他脾切除组及正常人群不同。在脾切除患者(>4年)中,血小板计数和淋巴细胞亚群增加,且随时间持续存在。因此,脾切除患者的这些血细胞计数与正常人群的参考值不同。

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本文引用的文献

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Neonatal thymectomy reveals differentiation and plasticity within human naive T cells.新生儿胸腺切除术揭示了人类初始T细胞的分化和可塑性。
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Diagnosis of infection after splenectomy for trauma should be based on lack of platelets rather than white blood cell count.创伤性脾切除术后感染的诊断应基于血小板减少而非白细胞计数。
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Blood clearance of Howell-Jolly bodies in an experimental autogenic splenic implant model.
胚系突变的 G 蛋白鉴定了 T 细胞中的信号串扰。
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A functional spleen contributes to afucosylated IgG in humans.功能性脾脏有助于人类去岩藻糖基化 IgG 的产生。
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Role of Partial Splenectomy in Hematologic Childhood Disorders.部分脾切除术在儿童血液系统疾病中的作用
Pathogens. 2021 Nov 5;10(11):1436. doi: 10.3390/pathogens10111436.
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Changes in peripheral lymphocyte populations in patients with advanced/recurrent ovarian cancer undergoing splenectomy during cytoreductive surgery.接受细胞减灭术的晚期/复发性卵巢癌患者脾切除术后外周血淋巴细胞群的变化。
J Ovarian Res. 2021 Aug 30;14(1):113. doi: 10.1186/s13048-021-00860-7.
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Dynamic hematological changes in patients undergoing distal pancreatectomy with or without splenectomy: a population-based cohort study.接受或不接受脾切除术的胰体尾切除术患者的动态血液学变化:基于人群的队列研究。
BMC Surg. 2020 Oct 31;20(1):265. doi: 10.1186/s12893-020-00931-4.
8
Immune thrombocytopenic purpura risk by live, inactivated and simultaneous vaccinations among Japanese adults, children and infants: a matched case-control study.日本成年人、儿童和婴儿中活疫苗、灭活疫苗和同时接种疫苗的免疫性血小板减少性紫癜风险:一项匹配病例对照研究。
Int J Hematol. 2020 Jul;112(1):105-114. doi: 10.1007/s12185-020-02866-1. Epub 2020 Apr 6.
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Post-splenectomy Sepsis: A Review of the Literature.脾切除术后脓毒症:文献综述
Cureus. 2020 Feb 6;12(2):e6898. doi: 10.7759/cureus.6898.
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Br J Surg. 2014 Jun;101(7):820-7. doi: 10.1002/bjs.9496. Epub 2014 Apr 23.
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Pediatr Blood Cancer. 2014 Jan;61(1):29-33. doi: 10.1002/pbc.24766. Epub 2013 Sep 13.
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Complement genetics, deficiencies, and disease associations.补体遗传学、缺陷与疾病关联。
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