Yodoi J, Ishizaka K
J Immunol. 1980 Mar;124(3):1322-9.
Culture of mesenteric lymph node cells from rats infected with Nippostrongylus brasiliensis resulted in the release of a soluble factor (IgE-binding factor) that can inhibit rosette formation of Fc epsilon R(+) lymphocytes with IgE-coated red cells. The factor is specifically absorbed with IgE-coated Sepharose. It has a m.w. of between 10,000 and 20,000. The major source of IgE-binding factor appears to be Fc epsilon R(+) T cells. The formation of IgE-binding factor by the lymphocytes was enhanced by IgE added to the culture medium. Evidence was obtained that Fc epsilon R(+) cells are involved in the induction of IgE-induced factor formation. Normal rat lymphocytes cultured alone failed to release IgE-binding factor, but incubation of normal lymphocytes with rat IgE resulted in the formation of IgE-binding factor and an increase in the proportion of Fc epsilon R(+) cells. It was also found that normal T cells formed the soluble factor upon incubation with IgE. In the induction of factor formation by normal lymphocytes, Fc gamma R(+) cells are essential; an Fc gamma R-depleted fraction failed to form IgE-binding factor upon incubation with IgE. The results suggest that interaction of IgE with Fc epsilon R(+) T cells and Fc gamma R(+) T cells induces the formation of IgE-binding factor(s).
用巴西日圆线虫感染大鼠后,对其肠系膜淋巴结细胞进行培养,结果释放出一种可溶性因子(IgE结合因子),该因子可抑制FcεR(+)淋巴细胞与IgE包被的红细胞形成玫瑰花结。该因子可被IgE包被的琼脂糖特异性吸附。其分子量在10,000至20,000之间。IgE结合因子的主要来源似乎是FcεR(+) T细胞。向培养基中添加IgE可增强淋巴细胞形成IgE结合因子的能力。有证据表明FcεR(+)细胞参与了IgE诱导的因子形成过程。单独培养的正常大鼠淋巴细胞未能释放IgE结合因子,但正常淋巴细胞与大鼠IgE一起孵育会导致IgE结合因子的形成以及FcεR(+)细胞比例的增加。还发现正常T细胞与IgE孵育后会形成可溶性因子。在正常淋巴细胞诱导因子形成的过程中,FcγR(+)细胞至关重要;去除FcγR的部分与IgE孵育后无法形成IgE结合因子。结果表明,IgE与FcεR(+) T细胞和FcγR(+) T细胞的相互作用诱导了IgE结合因子的形成。