抗原诱导的B淋巴细胞分化。

CRC Critical reviews in immunology Pub Date : 1982-02-01
M C Howard
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引用次数: 0

摘要

对于免疫学家和细胞生物学家来说,B淋巴细胞活化的分析一直是一个诱人的前景,因为B细胞具有具有良好特征的受体和对特定抗原表现出明确的诱导反应的独特特征。正如本文所概述的那样,我们现在对成熟B细胞在免疫能力强的宿主的外周淋巴器官内遇到抗原时发生的细胞事件有了更多的了解。我们对与这些细胞过程相关的分子事件的了解目前是有限的,但这样的信息无疑会随之而来。b细胞免疫学的最大挑战是免疫调节和理解巨大的b细胞特异性库是如何产生的。这些挑战需要更深入地了解淋巴细胞触发事件和b细胞成熟的早期事件。这篇综述并不局限于与抗原触发的成熟脾B细胞相关的现象,而是试图包括经常被忽视或忽视的B细胞发育方面。特别注意的是某些非特异性抗原诱导的b细胞事件,以及成熟b细胞发育之前的抗原启动的发育过程。此外,鉴于目前试图以避免终端分化的方式持续繁殖正常淋巴细胞,已经重新考虑了被触发的成熟B细胞对效应细胞产生的承诺。这些细胞系的可用性,加上日益完善的技术,将有希望让我们解决b细胞发育中剩余的谜团。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antigen-induced B lymphocyte differentiation.

The analysis of B-lymphocyte activation has been a tantalizing prospect for both immunologists and cell biologists, as B cells have the unique characteristics of possessing a well-characterized receptor and displaying a clear inducible response to a specific antigen. As outlined in this review, we now know much about the cellular events which occur when mature B cell encounters antigen within the peripheral lymphoid organ of an immunocompetent host. Our understanding of the molecular events associated with these cellular processes is currently limited, but such information will undoubtedly ensue. The greatest challenges remaining in B-cell immunology are immunoregulation and an understanding of how the enormous B-cell specificity repertoire is generated. These challenges require greater insight into lymphocyte triggering events and the early events in B-cell maturation. This review has not restricted itself to the phenomena associated with antigen-triggered mature splenic B cells, but has attempted to include aspects of B-cell development which are often overlooked or disregarded. In particular, attention has been drawn to certain nonspecific antigen-induced B-cell events, and to antigen-initiated developmental processes which precede mature B-cell development. Additionally, the commitment of triggered mature B cells to effector cell production has been reconsidered in light of current attempts to propagate normal lymphocytes continuously and in a manner which avoids terminal differentiation. The availability of such lines, together with increasingly refined technology, will hopefully allow us to resolve the remaining mysteries in B-cell development.

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