Baudouin Véronique, Crusiaux Alain, Haddad Elie, Schandene Liliane, Goldman Michel, Loirat Chantal, Abramowicz Daniel
Department of Nephrology, Hopital Robert Debré, Paris, France.
Transplantation. 2003 Aug 15;76(3):459-63. doi: 10.1097/01.TP.0000073809.65502.8F.
Repeated administration of chimeric or humanized monoclonal antibodies is generally well tolerated. Anti-idiotypic sensitization is rare and is considered to be of no clinical significance. We observed a child who experienced anaphylactic shock when he received a second course of basiliximab at the time of his second renal transplantation. We therefore searched for the presence of anti-basiliximab immunoglobulin (Ig) E in this patient.
Serum levels of anti-basiliximab IgE, assay of the anti-murine reactivity of circulating anti-basiliximab IgE, and assays for serum anti-mouse antibodies and global anti-basiliximab anti-idiotypic antibodies were carried out by enzyme-linked immunosorbent assay. Anti-basiliximab IgE antibodies on circulating basophils were evaluated by the ability of the patient's blood to produce leukotrienes in vitro after exposure to basiliximab.
Sequential assays of serum samples by enzyme-linked immunosorbent assay indicated that anti-basiliximab IgE antibodies appeared after the second basiliximab course. There was no IgE reactivity toward a control murine IgG2a monoclonal antibody (mAb), indicating that the IgE response was directed exclusively against basiliximab idiotypes. There was no IgE reactivity against the humanized anti-interleukin-2 receptor mAb daclizumab, which was derived from a distinct parental murine mAb. Patient basophils harvested months after the anaphylactic shock produced leukotrienes in vitro on exposure to basiliximab.
Patients exposed to chimeric antibodies may develop an anti-idiotypic IgE response that can trigger anaphylactic shock on further exposure. Specific anti-idiotypic IgE may be bound to basophils even in the absence of circulating IgE.
嵌合或人源化单克隆抗体的重复给药通常耐受性良好。抗独特型致敏很少见,且被认为无临床意义。我们观察到一名儿童在第二次肾移植时接受第二疗程巴利昔单抗时发生了过敏性休克。因此,我们在该患者中寻找抗巴利昔单抗免疫球蛋白(Ig)E的存在情况。
采用酶联免疫吸附测定法检测血清中抗巴利昔单抗IgE水平、循环抗巴利昔单抗IgE的抗鼠反应性,以及血清抗鼠抗体和总体抗巴利昔单抗抗独特型抗体。通过患者血液在体外接触巴利昔单抗后产生白三烯的能力来评估循环嗜碱性粒细胞上的抗巴利昔单抗IgE抗体。
酶联免疫吸附测定法对血清样本进行连续检测表明,抗巴利昔单抗IgE抗体在第二疗程巴利昔单抗治疗后出现。对对照鼠IgG2a单克隆抗体(mAb)无IgE反应性,表明IgE反应仅针对巴利昔单抗独特型。对源自不同亲本鼠mAb的人源化抗白细胞介素-2受体mAb达克珠单抗无IgE反应性。过敏性休克数月后采集的患者嗜碱性粒细胞在体外接触巴利昔单抗时产生白三烯。
接触嵌合抗体的患者可能会产生抗独特型IgE反应,再次接触时可引发过敏性休克。即使在无循环IgE的情况下,特异性抗独特型IgE也可能与嗜碱性粒细胞结合。