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X连锁重症联合免疫缺陷病(X-SCID)B细胞对白介素-4和白介素-13的反应由一种受体复合物介导,该复合物包含白介素-4受体α链(p140),但不包含γc链。

X-SCID B cell responses to interleukin-4 and interleukin-13 are mediated by a receptor complex that includes the interleukin-4 receptor alpha chain (p140) but not the gamma c chain.

作者信息

Matthews D J, Hibbert L, Friedrich K, Minty A, Callard R E

机构信息

Immunobiology Unit, Institute of Child Health, London, GB.

出版信息

Eur J Immunol. 1997 Jan;27(1):116-21. doi: 10.1002/eji.1830270118.

Abstract

This study investigates the effect of interleukin (IL)-4 mutant proteins and a monoclonal antibody to the IL-4 receptor alpha chain on IL-4 and IL-13 response by B cells from X-linked severe combined immunodeficiency (X-SCID) patients in which the common gamma chain (gamma c chain) gene mutations have been fully characterized and no gamma c chain expression was detected. In this gamma c chain gene knockout model, it was confirmed that the gamma c chain is essential for B cell responses to IL-2 but not for IL-4 or IL-13. Dose-response curves for X-SCID and normal B cell responses to IL-4 were indistinguishable, showing that the loss of the gamma c chain did not diminish the sensitivity of B cells to IL-4. The mutant protein IL-4(Y124D) and an antibody to the IL-4R alpha chain both inhibited responses of X-SCID B cells to IL-4 and IL-13, showing that X-SCID B cell responses to these cytokines are mediated by a receptor complex that includes the IL-4R alpha chain but not the gamma c chain. Another mutant protein, IL-4(R88D), which has greatly reduced affinity for IL-4R alpha, was found to inhibit responses by normal B cells to IL-4 but not to IL-13. IL-4(R88D), did not, however, inhibit X-SCID B cell responses to IL-4. This result is consistent with IL-4(R88D) inhibition of responses mediated by receptor complexes that include the gamma c chain. We propose that X-SCID B cells responses to IL-4 are mediated by an IL-13 receptor complex comprised of the IL-4R alpha chain associated with the recently cloned IL-13R binding protein. This model has major implications for understanding normal B cell responses to IL-4.

摘要

本研究调查了白细胞介素(IL)-4突变蛋白和抗IL-4受体α链单克隆抗体对X连锁严重联合免疫缺陷(X-SCID)患者B细胞IL-4和IL-13反应的影响,这些患者的共同γ链(γc链)基因突变已得到充分表征,且未检测到γc链表达。在这个γc链基因敲除模型中,证实了γc链对于B细胞对IL-2的反应至关重要,但对IL-4或IL-13的反应并非必需。X-SCID和正常B细胞对IL-4的剂量反应曲线没有差异,表明γc链的缺失并未降低B细胞对IL-4的敏感性。突变蛋白IL-4(Y124D)和抗IL-4Rα链抗体均抑制X-SCID B细胞对IL-4和IL-13的反应,表明X-SCID B细胞对这些细胞因子的反应是由包含IL-4Rα链但不包含γc链的受体复合物介导的。另一种对IL-4Rα亲和力大大降低的突变蛋白IL-4(R88D),被发现可抑制正常B细胞对IL-4的反应,但不能抑制对IL-13的反应。然而,IL-4(R88D)并未抑制X-SCID B细胞对IL-4的反应。这一结果与IL-4(R88D)抑制由包含γc链的受体复合物介导的反应一致。我们提出,X-SCID B细胞对IL-4的反应是由一种IL-13受体复合物介导的,该复合物由与最近克隆的IL-13R结合蛋白相关的IL-4Rα链组成。该模型对于理解正常B细胞对IL-4的反应具有重要意义。

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