Clark S J, Law D A, Paterson D J, Puklavec M, Williams A F
Medical Research Council Cellular Immunology Research Unit, Sir William Dunn School of Pathology, Oxford, England.
J Exp Med. 1988 Jun 1;167(6):1861-72. doi: 10.1084/jem.167.6.1861.
Rat T cells and thymocytes were induced to proliferate by a pair of mAbs, MRC OX-54 and MRC OX-55, directed against rat CD2. Accessory cells were required but their role was not simply for crosslinking of the two mAbs, as neither MRC OX-54 nor MRC OX-55 alone, in the presence of a crosslinking second antibody, caused T cell mitogenesis. Nor could the phorbol ester PMA replace either antibody. The two mAbs recognized distinct epitopes on rat CD2; however, MRC OX-54 could partially block MRC OX-55 binding whereas the reverse situation was not seen. A further CD2 epitope was recognized by two mutually competitive mAbs, MRC OX-34 and MRC OX-53, which were not mitogenic. Neither MRC OX-34 nor MRC OX-53 affected the binding of MRC OX-54 or MRC OX-55, yet they prevented the mitogenic effect induced by these mAbs. The presence of mAbs against CD4 and the IL-2-R also abrogated this mitogenesis, whereas an anti-CD5 mAb augmented the CD2-induced proliferation.
一对针对大鼠CD2的单克隆抗体MRC OX - 54和MRC OX - 55可诱导大鼠T细胞和胸腺细胞增殖。需要辅助细胞,但它们的作用不仅仅是使这两种单克隆抗体发生交联,因为在存在交联二抗的情况下,单独的MRC OX - 54或MRC OX - 55都不会引起T细胞有丝分裂。佛波酯PMA也不能替代任何一种抗体。这两种单克隆抗体识别大鼠CD2上不同的表位;然而,MRC OX - 54可部分阻断MRC OX - 55的结合,而反之则未观察到。另外一个CD2表位被两种相互竞争的非促有丝分裂单克隆抗体MRC OX - 34和MRC OX - 53识别。MRC OX - 34和MRC OX - 53都不影响MRC OX - 54或MRC OX - 55的结合,但它们可阻止这些单克隆抗体诱导的促有丝分裂效应。抗CD4和抗IL - 2 - R单克隆抗体的存在也消除了这种有丝分裂,而抗CD5单克隆抗体则增强了CD2诱导的增殖。