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CD40及其配体GP39的免疫调节作用

Immune regulation by CD40 and its ligand GP39.

作者信息

Foy T M, Aruffo A, Bajorath J, Buhlmann J E, Noelle R J

机构信息

Department of Microbiology, Dartmouth Medical School, Lebanon, New Hampshire 03756, USA.

出版信息

Annu Rev Immunol. 1996;14:591-617. doi: 10.1146/annurev.immunol.14.1.591.

Abstract

Over the past three years, CD40 and its ligand (gp39, CD40L, TBAM) have been shown to be essential for humoral immune responses to thymus-dependent antigens. However, as the tissue distribution widens for those cells that express CD40 and gp39, we can now show that this ligand-receptor pair also plays an important role in the selection of self-reactive T cells in the thymus (central tolerance) and the regulation of tolerance in mature T cells (peripheral tolerance). Advances in our understanding of the molecular basis for CD40 biology is based in two areas of research. First, a major breakthrough in our understanding of how CD40 transduces biological events centers on the identification of a novel protein that binds to the cytoplasmic tail of CD40 and may act as a signal transducing molecule. Secondly, advances in molecular modeling and mutagenesis of this ligand-receptor pair have helped to identify the critical receptor/ligand contacts in the gp39/CD40 complex. Advances in each of these areas are discussed.

摘要

在过去三年中,已证明CD40及其配体(gp39、CD40L、TBAM)对于针对胸腺依赖性抗原的体液免疫反应至关重要。然而,随着表达CD40和gp39的细胞的组织分布范围扩大,我们现在可以证明,这种配体-受体对在胸腺中自身反应性T细胞的选择(中枢耐受)以及成熟T细胞的耐受调节(外周耐受)中也起着重要作用。我们对CD40生物学分子基础的理解进展基于两个研究领域。首先,我们对CD40如何转导生物学事件的理解取得了重大突破,其核心在于鉴定出一种与CD40细胞质尾部结合并可能作为信号转导分子的新型蛋白质。其次,该配体-受体对的分子建模和诱变方面的进展有助于确定gp39/CD40复合物中的关键受体/配体接触点。将对这两个领域的进展进行讨论。

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