Sehon A H, Lee W Y
Ann Immunol (Paris). 1977 Jan-Mar;128(1-2):457-68.
The primary as well as an ongoing IgE response to the haptens--2,4-dinitrophenyl (DNP) and benzylpénicilloyl (BPO) determinants--were readily abrogated in an immunologically specific manner by the administration of conjugates consisting of the corresponding hapten coupled to the isologous, non-immunogenic murine gamma globulins (MgammaG), i. e., DNP8-MgammaG or BPO9-MgammaG. The epitope density of the DNPx-MgammaG and BPOx-MgammaG was shown to play a dominant role in determining whether or not these conjugates were tolerogenic. Using the adoptive transfer system in mice, it was demonstrated that this method of immunosuppression was not due to the formation of suppressor cells, but involved the elimination of hapten specific IgE-forming Bepsilon cells or the inactivation of these cells through the blockade of their antigen binding receptors. This method of suppression of anti-hapten IgE antibodies, by the use of conjugates of haptens with isologous gamma-globulins, proved also effective in rats and dogs.
对2,4 -二硝基苯基(DNP)和苄青霉素酰(BPO)决定簇等半抗原的主要以及持续的IgE反应,通过给予由相应半抗原与同种、无免疫原性的小鼠γ球蛋白(MγG)偶联而成的缀合物,即DNP8 - MγG或BPO9 - MγG,能够以免疫特异性方式轻易消除。DNPx - MγG和BPOx - MγG的表位密度在决定这些缀合物是否具有致耐受性方面起着主导作用。利用小鼠的过继转移系统证明,这种免疫抑制方法并非由于抑制细胞的形成,而是涉及消除半抗原特异性IgE形成Bε细胞或通过阻断其抗原结合受体使这些细胞失活。通过使用半抗原与同种γ球蛋白的缀合物来抑制抗半抗原IgE抗体的这种方法,在大鼠和狗中也证明是有效的。