Role of Chemokine Signalling in the Pathogenesis of Good's Syndrome-CaseReports, Clinical Characterization from Single-Centre Perspective

P. Zdziarski, G. Dworacki, A. Korzeniowska-Kowal, K. Ziemnicka
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引用次数: 4

Abstract

Good’s syndrome (GS), is a rare condition defined as a coexistence of thymoma and hipogammaglobulinaemia. Involvement of central lymphoid organ prompts concept about perturbation in lymphocyte migration and differentiation. Cell homing to bone marrow compartment depends on the CXCR4↔CXCL12 interaction. In this paper we describe two patients with GS-mild and severe form, presenting differences in the expression of CXCR4 on cells in peripheral blood and bone marrow. Patient 1 (mild form): (i) Mild hipogammaglobulinaemia (IgG=150 mg/dL), (ii) Low count of peripheral B cells (14%, 60 cells/μL) and NK (18%, 77cells/μL); high level of T cells (93.3%, 4006 cells/ μL), (iii) Moderate thymic enlargement (9 × 15 cm), (iv) CXCR4 expression in BM 82.6% (20139/μL), 34% CXCR4+CD19+ (8289/μL). Patient 2 (severe form): (i) Severe hipogammaglobulinaemia (IgG=20 mg/dL), (ii) Absence of B and NK cells deficiency (in peripheral blood 0.4% i.e., 10/μL, and 6.17%-47.3/μL respectively), (iii) Severe thymic enlargement (20 × 25 cm) (iv) CXCR4 expression in BM 46.3% (552/μL); 6.1%, CXCR4+CD19+ (174/ μL). Interestingly, the bone marrow of patient with severe form of GS contained more CD10-positive B cells than BM of the patient with mild form (80% vs. 5.88% of B cells), but in former as well as letter a significant proportion of the total CXCR4-positive lymphocytes are negative for B cells marker (comparable: 48.1% and 53.1% respectively). In our patients a tenfold decrease in the CD4-positive γδ T cells (CD4+TCRγδ) counts was observed. Both cases went up fatal due to progression of nasopharyngeal cancer (mild form) and breast cancer (severe form). This data confirm that earliest B cell precursors, pre-pro-B cells and end-stage B cells, plasma cells require CXCR4 ↔ CXCL12 interaction. In contrast in GS weak expression of CXCR4 in marrow precursors is source of B cell differentiation arrest on pro-B cell stage. The low level Nk and CD4+γδ T cells in Good syndrome is the new observation.
趋化因子信号在Good's综合征发病机制中的作用-病例报告,单中心视角的临床特征
古德氏综合征(GS)是一种罕见的胸腺瘤和高γ球蛋白血症共存的疾病。中枢淋巴器官的受累提示了淋巴细胞迁移和分化的扰动概念。细胞归巢到骨髓室依赖于CXCR4↔CXCL12的相互作用。在本文中,我们描述了两例gs -轻度和重度形式的患者,外周血和骨髓细胞中CXCR4的表达存在差异。患者1(轻度):(i)轻度hipogammagglobullinemia (IgG=150 mg/dL), (ii)外周血B细胞计数低(14%,60个细胞/μL), NK细胞计数低(18%,77个细胞/μL);(iii)胸腺适度增大(9 × 15 cm), (iv) CXCR4在BM中表达82.6% (20139/μL), CXCR4+CD19+表达34% (8289/μL)。患者2(严重型):(i)严重的大γ球蛋白血症(IgG=20 mg/dL), (ii)缺乏B细胞和NK细胞缺乏(外周血中分别为0.4%,即10/μL和6.17%-47.3/ l), (iii)严重胸腺肿大(20 × 25 cm) (iv) CXCR4在BM中表达46.3% (552/μL);6.1%, cxcr4 + cd19 + (174/ μl)。有趣的是,重度GS患者骨髓中cd10阳性B细胞比轻度GS患者骨髓中cd10阳性B细胞多(80%比5.88%),但前者和后者中cxcr4阳性淋巴细胞中B细胞标记物阴性的比例显著(分别为48.1%和53.1%)。在我们的患者中,观察到CD4阳性γδ T细胞(CD4+TCRγδ)计数减少了10倍。由于鼻咽癌(轻度形式)和乳腺癌(严重形式)的进展,这两个病例都死亡了。这一数据证实最早的B细胞前体、前-前B细胞和终末期B细胞、浆细胞需要CXCR4↔CXCL12的相互作用。相比之下,在GS中,骨髓前体细胞中CXCR4的弱表达是前B细胞阶段B细胞分化受阻的来源。在Good综合征中Nk和CD4+γδ T细胞的低水平是新的观察。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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