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针对人类B细胞淋巴瘤产生单克隆抗独特型抗体的策略。

Strategies for production of monoclonal anti-idiotype antibodies against human B cell lymphomas.

作者信息

Thielemans K, Maloney D G, Meeker T, Fujimoto J, Doss C, Warnke R A, Bindl J, Gralow J, Miller R A, Levy R

出版信息

J Immunol. 1984 Jul;133(1):495-501.

PMID:6609992
Abstract

Murine monoclonal antibodies (MAB) against the idiotype (Id) of B lymphocyte malignancies are powerful reagents for the study of these diseases, and are potentially useful for treatment. Different strategies for the production of these anti-Id MAB have been compared. Initially, the Id Ig from nonsecreting B cell tumors was "rescued" by human X mouse or human X human hybridization. These somatic cell hybridizations resulted in the secretion of human Ig in 10 and 100% of the fusions, respectively. In a second step, anti-Id MAB were produced by using the "rescued" Id Ig as immunogen. A more streamlined approach is based on a one-step procedure in which the tumor cell suspension is used as immunogen. This method of immunization, coupled with a four-layer ELISA, results in the detection of anti-Id MAB in a frequency of approximately 1% of the total hybrids. By using a pool of 10 different anti-Id MAB, each reactive with the tumor of one patient, we searched for idiotypic relatedness among a panel of 50 additional tumors. No cross-reactions were found, indicating that our current strategy results in the identification of unique idiotypic determinants among human B cell tumors. Idiotypic Ig can be found in the serum of patients with B cell tumors. Among groups of patients, there is a wide spectrum of serum Id levels, ranging from less than 0.01 microgram/ml to greater than 500 micrograms/ml.

摘要

针对B淋巴细胞恶性肿瘤独特型(Id)的鼠单克隆抗体(MAB)是研究这些疾病的有力试剂,并且可能对治疗有用。已比较了产生这些抗Id MAB的不同策略。最初,通过人X小鼠或人X人杂交“拯救”来自非分泌性B细胞肿瘤的Id Ig。这些体细胞杂交分别在10%和100%的融合体中导致人Ig的分泌。第二步,通过使用“拯救”的Id Ig作为免疫原产生抗Id MAB。一种更简化的方法基于一步程序,其中将肿瘤细胞悬液用作免疫原。这种免疫方法与四层ELISA相结合,导致在约1%的总杂交体中检测到抗Id MAB。通过使用一组10种不同的抗Id MAB,每种与一名患者的肿瘤反应,我们在另外50个肿瘤的一组中寻找独特型相关性。未发现交叉反应,表明我们目前的策略导致在人B细胞肿瘤中鉴定出独特的独特型决定簇。独特型Ig可在B细胞肿瘤患者的血清中发现。在患者组中,血清Id水平范围很广,从小于0.01微克/毫升到大于500微克/毫升。

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