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免疫球蛋白在进化过程中并非为对抗感染而产生。

Immunoglobulins did not arise in evolution to fight infection.

作者信息

Stewart J

机构信息

Unité d'Immunobiologie, CNRS URA 359, Institut Pasteur, Paris, France.

出版信息

Immunol Today. 1992 Oct;13(10):396-9; discussion 399-400. doi: 10.1016/0167-5699(92)90088-O.

DOI:10.1016/0167-5699(92)90088-O
PMID:1418375
Abstract

The complex interactions between B and T cells in response to external antigens are the major focus of contemporary immunology. Here, John Stewart argues that they may be relatively late evolutionary developments, due to the redeployment of a system invented for other reasons. He suggests that the system of variable region molecules (VRM) arose, at the time of the first vertebrates, by an endogenous, self-organizing process; this primordial VRM system instituted a molecular ecology, a function so important that from then on no vertebrate has been able to do without it.

摘要

B细胞和T细胞对外源抗原的复杂相互作用是当代免疫学的主要研究重点。在此,约翰·斯图尔特认为,由于为其他目的而发明的系统被重新部署,它们可能是相对较晚出现的进化产物。他提出,可变区分子(VRM)系统在第一批脊椎动物出现时,通过内源性的自组织过程产生;这个原始的VRM系统建立了一种分子生态,其功能如此重要,以至于从那时起,没有任何脊椎动物能够离开它而生存。

相似文献

1
Immunoglobulins did not arise in evolution to fight infection.免疫球蛋白在进化过程中并非为对抗感染而产生。
Immunol Today. 1992 Oct;13(10):396-9; discussion 399-400. doi: 10.1016/0167-5699(92)90088-O.
2
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Natural recognition repertoire and the evolutionary emergence of the combinatorial immune system.天然识别库与组合免疫系统的进化出现
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[The antigen recognition mechanism and regulation of immune responses].[抗原识别机制与免疫反应的调节]
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Ig domains 1 and 2 of murine CD22 constitute the ligand-binding domain and bind multiple sialylated ligands expressed on B and T cells.小鼠CD22的免疫球蛋白结构域1和2构成配体结合结构域,并与B细胞和T细胞上表达的多种唾液酸化配体结合。
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