Brüggemann M, Winter G, Waldmann H, Neuberger M S
Department of Pathology, Addenbrooke's Hospital, Cambridge, United Kingdom.
J Exp Med. 1989 Dec 1;170(6):2153-7. doi: 10.1084/jem.170.6.2153.
Mice were immunized with model xenogeneic (both the VH frameworks and the CH domains of human origin), chimeric (just VH frameworks human), or self antibodies, and the antiantibody responses were dissected. Only the self antibody did not elicit a response. A strong response was elicited by the most xenogeneic antibody with approximately 90% against the C and approximately 10% against the V. The anti-V response was not attenuated in the chimeric antibody, demonstrating that foreign VH frameworks can be sufficient to lead to a strong antiantibody response. The magnitude of this xenogeneic anti-VH response was similar to that of the allotypic response elicited by immunizing mice of the Igha allotype with an Ighb antibody. Thus, although chimerization can diminish antiantibody responses, attention should be paid both to V region immunogenicity and to polymorphism.
用模型异种抗体(人源的VH框架区和CH结构域)、嵌合抗体(仅VH框架区是人源的)或自身抗体免疫小鼠,并分析抗抗体反应。只有自身抗体未引发反应。最具异种性的抗体引发了强烈反应,约90%针对C区,约10%针对V区。嵌合抗体中的抗V区反应并未减弱,这表明外来的VH框架区足以引发强烈的抗抗体反应。这种异种抗VH反应的强度与用Ighb抗体免疫Igha同种异型小鼠所引发的同种异型反应相似。因此,虽然嵌合化可减少抗抗体反应,但应同时关注V区的免疫原性和多态性。