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来自原发性免疫缺陷疾病患者的爱泼斯坦-巴尔病毒诱导的淋巴母细胞系。

Epstein-Barr virus-induced lymphoblastoid cell lines from patients with primary immunodeficiency diseases.

作者信息

Tsuchiya S, Konno T, Tada K, Ono Y

机构信息

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Scand J Immunol. 1980;11(2):155-62. doi: 10.1111/j.1365-3083.1980.tb00221.x.

Abstract

Peripheral lymphocytes from eight patients with congenital immunodeficiency diseases were infected with Epstein-Barr virus (EBV) in an attempt to establish B lymphoblastoid cell lines (LCL). These patients included three boys with congenital agammaglobulinaemia, two girls with hypogammaglobulinaemia, one boy with common variable immunodeficiency, one boy with severe combined immunodeficiency with adenosine deaminase deficiency, and one boy with DiGeorge syndrome. Five of the patients bore no surface immunoglobulins (sIg) on their peripheral lymphocytes. LCL were established from seven of the eight patients. All the LCL established formed rosettes with EAC3 and had the ability to produce cytoplasmic immunoglobulins (cIg) of various classes. Culture supernatants concentrated up to 100-fold developed precipitin bands by Ouchterlony's method with antisera to human Ig in all the established LCL. These results suggested that both sIg-, cIg- and C3+ cells and sIg+, cIg- and C3+ cells might be the target cells for EBV and that sIg-, cIg- and C3+ cells might be the precursor cells of B lymphocytes.

摘要

为了建立B淋巴母细胞系(LCL),用爱泼斯坦-巴尔病毒(EBV)感染了8例先天性免疫缺陷疾病患者的外周淋巴细胞。这些患者包括3例先天性无丙种球蛋白血症男孩、2例低丙种球蛋白血症女孩、1例普通可变免疫缺陷男孩、1例伴有腺苷脱氨酶缺乏的严重联合免疫缺陷男孩和1例迪格奥尔格综合征男孩。其中5例患者外周淋巴细胞表面无表面免疫球蛋白(sIg)。8例患者中有7例建立了LCL。所有建立的LCL均与EAC3形成玫瑰花结,并具有产生各类细胞质免疫球蛋白(cIg)的能力。通过奥克特洛尼法,在所有建立的LCL中,浓缩至100倍的培养上清液与抗人Ig抗血清产生沉淀带。这些结果表明,sIg-、cIg-和C3+细胞以及sIg+、cIg-和C3+细胞可能都是EBV的靶细胞,且sIg-、cIg-和C3+细胞可能是B淋巴细胞的前体细胞。

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