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Influence of drug molecules on regulatory B cells

机译:药物分子对调节B细胞的影响

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摘要

Abstract By their suppressive functions, regulatory B (Breg) cells are considered as key elements in the control and development of various disease states. Many signals can induce Bregs in vivo and in vitro and often from heterogeneous populations. Several specific signals delivered in a timely immunological context contribute to the establishment of Bregs. These are endogenous and physiological signals or stimuli, widely discussed in the literature participating in the establishment of an effective immune response. However, exogenous signals, much less clearly identified can also be considered as Bregs inducers. These extrinsic signals are capable of directly or indirectly influencing the suppressive capacity of Bregs, but also their expansion and functional restoration in its absence. Faced with the excitement generated by the development of processes favoring the expansion of Bregs in mice for therapeutic purposes, the challenge today is to extrapolate such approaches in humans. This perspective may already be in effect. Highlights ? Breg cells control autoimmunity, allergy, infection or cancer development. ? Breg cells can be endogenously activated by BCR, CD40 and/or TLR stimulation. ? Various exogenous drugs and immunotherapies induce Breg cell functions. ? Efficiency of future therapeutics should appraise their influence on Bregs.
机译:摘要通过其抑制功能,调节B(BREG)细胞被认为是各种疾病状态控制和发展的关键要素。许多信号可以在体内和体外诱导坯料,并且通常来自异质群体。在及时的免疫背景下交付的几个特定信号有助于建立贫困人口。这些是内源性和生理信号或刺激,在参与建立有效免疫应答的文献中广泛讨论。然而,外源性信号,更清楚地识别也可以被视为Bregs诱导剂。这些外本信号能够直接或间接地影响贫氏的抑制能力,也能够在缺失中进行膨胀和功能恢复。面对兴奋产生的流程,青睐小鼠在治疗目的中的小鼠扩张的过程中,今天的挑战是推断人类的这种方法。这个角度可能已经有效。强调 ? BREG细胞控制自身免疫,过敏,感染或癌症发展。还BCR,CD40和/或TLR刺激可以内源性激活BREG细胞。还各种外源药物和免疫疗法诱导伯格细胞功能。还未来治疗方法的效率应评估它们对贫困人口的影响。

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