Reed-Loisel Lisa M, Sullivan Barbara A, Laur Oskar, Jensen Peter E
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Immunol. 2005 Jun 15;174(12):7746-52. doi: 10.4049/jimmunol.174.12.7746.
TCR transgenic 6C5 T cells recognize an insulin B chain epitope presented by the nonclassical class I MHC molecule, Qa-1(b). Positive selection of these T cells was shown previously to require Qa-1(b). Despite dedicated specificity for Qa-1(b), evidence presented in the current study indicates that 6C5 T cells can cross-recognize a classical class I molecule. Clonal deletion was observed unexpectedly in 6C5.H-2(bxq) mice, which do not express I-E MHC class II molecules and thus should not be subject to superantigen-mediated negative selection. 6C5 T cells were observed to respond in vivo and in vitro to spleen cells from allogeneic H-2(q) mice, and specificity was mapped to D(q). Evidence was obtained for direct recognition of D(q), rather than indirect presentation of a D(q)-derived peptide presented by Qa-1(b). Polyclonal CD8(+) T cells from class Ia-deficient K(b)D(b-/-) mice reacted in vitro to allogeneic spleen cells with an apparent frequency comparable to conventional class Ia-restricted T cells. Our results provide a clear example of a Qa-1-specific TCR that can cross-react with a class Ia molecule and evidence supporting the idea that this may be a common property of T cells selected by class Ib molecules.
TCR转基因6C5 T细胞识别由非经典I类MHC分子Qa-1(b)呈递的胰岛素B链表位。先前已表明这些T细胞的阳性选择需要Qa-1(b)。尽管对Qa-1(b)具有专一的特异性,但本研究提供的证据表明6C5 T细胞能够交叉识别一种经典I类分子。在不表达I-E MHC II类分子因而不应受到超抗原介导的阴性选择的6C5.H-2(bxq)小鼠中意外观察到克隆清除。观察到6C5 T细胞在体内和体外对同种异体H-2(q)小鼠的脾细胞产生反应,并且特异性定位于D(q)。获得了直接识别D(q)的证据,而不是由Qa-1(b)呈递的源自D(q)的肽的间接呈递。来自Ia类缺陷型K(b)D(b-/-)小鼠的多克隆CD8(+) T细胞在体外对同种异体脾细胞产生反应,其明显频率与传统的Ia类限制性T细胞相当。我们的结果提供了一个Qa-1特异性TCR能够与Ia类分子发生交叉反应的清晰例子,并支持了这可能是由Ib类分子选择的T细胞的共同特性这一观点的证据。