Liao L, Marinescu A, Molano A, Ciurli C, Sekaly R P, Fraser J D, Popowicz A, Posnett D N
Department of Medicine, Graduate School of Medical Sciences, Cornell University Medical College, New York 10021, USA.
J Exp Med. 1996 Oct 1;184(4):1471-82. doi: 10.1084/jem.184.4.1471.
Both superantigens (SAG) and many anti-TCR monoclonal antibodies (mAb) have specificity for the V beta region of the TCR encoded by TCRBV genes. For instance the bacterial SAG staphylococcal enterotoxin E (SEE), the retroviral SAG MTV-9 and the mAb OT145 each react with human T cells expressing BV6S7. This BV gene encodes two common alleles. We found that SEE and the mAb preferentially activate T cells expressing BV6S71 as opposed to BV6S72, but Mtv-9 activates T cells expressing either allele. Thus binding to the TCR differs between the two SAGs. A mutation in the TCR HVR-4 region of BV6S71 (G72E), where the two BV6S7 alleles differ, indicated that HVR-4 is a component of the binding site for SEE and for the mAb OT145. BV6S72 has a charged E72 which may result in electrostatic repulsion of SEE, as SEE contains a similarly acidic aspartic acid residue at a TCR interaction site (204D).
超抗原(SAG)和许多抗TCR单克隆抗体(mAb)都对由TCRBV基因编码的TCR的Vβ区域具有特异性。例如,细菌超抗原葡萄球菌肠毒素E(SEE)、逆转录病毒超抗原MTV-9和单克隆抗体OT145都与表达BV6S7的人T细胞发生反应。该BV基因编码两个常见等位基因。我们发现,SEE和单克隆抗体优先激活表达BV6S71而非BV6S72的T细胞,但Mtv-9可激活表达任一等位基因的T细胞。因此,两种超抗原与TCR的结合存在差异。BV6S71的TCR高变区4(HVR-4)区域(G72E)发生突变,这两个BV6S7等位基因在此处存在差异,表明HVR-4是SEE和单克隆抗体OT145结合位点的一个组成部分。BV6S72具有带电荷的E72,这可能导致SEE产生静电排斥,因为SEE在TCR相互作用位点(204D)含有一个类似的酸性天冬氨酸残基。