首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Crosstalk between alpha/beta T cells and gamma/delta T cells in vivo: activation of alpha/beta T-cell responses after gamma/delta T-cell modulation with the monoclonal antibody GL3.
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Crosstalk between alpha/beta T cells and gamma/delta T cells in vivo: activation of alpha/beta T-cell responses after gamma/delta T-cell modulation with the monoclonal antibody GL3.

机译:体内α/βT细胞与γ/δT细胞之间的串扰:在用单克隆抗体GL3进行γ/δT细胞调节后α/βT细胞反应的激活。

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摘要

Although gamma/delta T cells express numerous in vitro functions similar to alpha/beta T cells, little is known about their biological functioning in vivo. Furthermore, it is unclear whether alpha/beta T cells and gamma/delta T cells act independently or in a coordinated way. In the present study, gamma/delta T cells were modulated in vivo by i.p. injection of the anti-gamma/delta T-cell receptor (TCR) monoclonal antibody GL3. GL3 administration caused disappearance of the gamma/delta TCR in spleen and lymph node cells and the gamma/delta TCR was reexpressed after in vitro cultivation for a few days. When cultured in vitro for 4 days, in the absence of foreign antigens, spleen and lymph node alpha/beta T cells from GL3-modulated mice showed vigorous proliferative responses. CD4 T lymphocytes from GL3-modulated mice produced interleukin 2, and CD8 T cells developed into cytolytic T lymphocytes in vitro capable of lysing syngeneic and allogeneic targets. Treatment with heat-inactivated GL3 or with normal hamster immunoglobulin did not cause any of these effects. These findings suggest that the anti-gamma/delta TCR monoclonal antibody GL3 modulates gamma/delta T cells in vivo and that this modulation has profound effects on alpha/beta T-cell reactivity. Hence, the data suggest a role for gamma/delta T cells in the regulation of alpha/beta T-cell activation in vivo.
机译:尽管γ/δT细胞表达出许多类似于α/βT细胞的体外功能,但对其在体内的生物学功能知之甚少。此外,尚不清楚α/βT细胞和γ/δT细胞是独立发挥作用还是协同作用。在本研究中,γ/δT细胞在体内通过腹膜内调节。注射抗γ/δT细胞受体(TCR)单克隆抗体GL3。 GL3给药导致脾和淋巴结细胞中的γ/δTCR消失,在体外培养几天后,γ/δTCR重新表达。当在体外培养4天时,在没有外来抗原的情况下,来自GL3调节的小鼠的脾脏和淋巴结α/βT细胞表现出强烈的增殖反应。来自GL3调节的小鼠的CD4 T淋巴细胞产生白介素2,而CD8 T细胞在体外发展成能够溶解同基因和同种异体靶标的细胞溶解性T淋巴细胞。用热灭活的GL3或正常的仓鼠免疫球蛋白治疗不会引起任何这些影响。这些发现表明,抗γ/δTCR单克隆抗体GL3在体内调节γ/δT细胞,并且这种调节对α/βT细胞反应性具有深远的影响。因此,数据表明γ/δT细胞在体内α/βT细胞活化的调节中起作用。

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