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“克隆”细胞群体产生抗体。

Antibody production by 'cloned' cell populations.

作者信息

Feldman M, Mekori T

出版信息

Immunology. 1966 Feb;10(2):149-60.

Abstract

A method for the instrasplenic cloning of lymph node cells, based on the injection into X-irradiated recipients of cells from phytohaemagglutinin treated donors was developed. Clones were tested for their capacity to form anti-Shigella antibodies, and to produce a graft versus host immune response. It was found that each of the randomly chosen clones produced antibodies to Shigella. When immunized `cloned' cell populations were injected into secondary recipients, and the latter were again immunized with Shigella, an increased response was obtained. Clones produced by bone marrow cells in spleens of X-irradiated animals, similarly tested for the immunological competence did not produce antibodies to Shigella. Cells of lymphoid clones of parental strain origin produced a graft versus host response in newborn F hybrids. Bone marrow derived clones did not. Thus, each cloned cell population appears to be pluripotential with respect to antibody formation. The immunological findings, analysed in relation to the population sizes of the tested clones, seem to indicate that each immune competent cell may, in fact, be pluripotential.

摘要

基于将经植物血凝素处理的供体的细胞注射到经X射线照射的受体中,开发了一种用于脾脏内克隆淋巴结细胞的方法。对克隆体进行了形成抗志贺氏菌抗体的能力以及产生移植物抗宿主免疫反应的测试。发现随机选择的每个克隆体都产生针对志贺氏菌的抗体。当将免疫的“克隆”细胞群体注射到二级受体中,并且后者再次用志贺氏菌免疫时,获得了增强的反应。对经X射线照射的动物脾脏中的骨髓细胞产生的克隆体进行类似的免疫能力测试,未发现产生针对志贺氏菌的抗体。亲本菌株来源的淋巴克隆细胞在新生F杂种中产生移植物抗宿主反应。骨髓来源的克隆体则不会。因此,就抗体形成而言,每个克隆的细胞群体似乎都具有多能性。根据测试克隆体的群体大小进行分析的免疫学发现似乎表明,实际上每个免疫活性细胞可能都是多能性的。

相似文献

3
[Antibody formation in a cell culture in vivo].
Usp Sovrem Biol. 1967 Jan-Feb;63(1):110-34.

本文引用的文献

1
THE MOLECULAR BASIS OF ANTIBODY FORMATION.抗体形成的分子基础。
Proc Natl Acad Sci U S A. 1960 Mar;46(3):293-302. doi: 10.1073/pnas.46.3.293.
4
ANTIBODY FORMATION AND THE CODING PROBLEM.抗体形成与编码问题。
Nature. 1965 Feb 27;205:847-51. doi: 10.1038/205847a0.
7
A DARWINIAN APPROACH TO IMMUNITY.一种关于免疫的达尔文主义方法。
Nature. 1964 Aug 1;203:451-4. doi: 10.1038/203451a0.

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