Schott Eckart, Bertho Nicolas, Ge Qing, Maurice Madelon M, Ploegh Hidde L
Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13735-40. doi: 10.1073/pnas.212515399. Epub 2002 Oct 8.
Crosslinking of the T cell receptor has been proposed to be a prerequisite for T cell activation. Although the evidence supports this notion for CD4 T cells, the situation for CD8 T cells is less clear. Soluble class I monomers have been used to determine activation requirements in vitro with contradictory results. The possibility of transfer of peptide from soluble class I molecules onto class I molecules present on the surface of CD8 T cells, with ensuing presentation to other CD8 T cells, has been widely ignored. We show that monomeric and tetrameric class I molecules as well as free peptide can stimulate naive CD8 T cells in vitro. We generate and characterize CD8 T cells that express the OT-I T cell receptor (for K(b)/SIINFEKL) yet lack K(b) and D(b) molecules, and show that their activation requirements differ from their class I positive counterparts when stimulated with soluble K(b) molecules. By eliminating the confounding effect of peptide transfer, we unmask the true activation requirements for naive CD8 T cells and show that multivalent engagement of T cell receptors, as well as costimulation, is required for optimal stimulation.
T细胞受体的交联已被认为是T细胞活化的先决条件。尽管有证据支持CD4 T细胞的这一观点,但CD8 T细胞的情况尚不清楚。可溶性I类单体已被用于体外确定活化要求,但结果相互矛盾。肽从可溶性I类分子转移到CD8 T细胞表面存在的I类分子上,随后呈递给其他CD8 T细胞的可能性一直被广泛忽视。我们发现单体和四聚体I类分子以及游离肽在体外均可刺激初始CD8 T细胞。我们生成并鉴定了表达OT-I T细胞受体(针对K(b)/SIINFEKL)但缺乏K(b)和D(b)分子的CD8 T细胞,并表明当用可溶性K(b)分子刺激时,它们的活化要求与其I类阳性对应物不同。通过消除肽转移的混杂效应,我们揭示了初始CD8 T细胞真正的活化要求,并表明T细胞受体的多价结合以及共刺激对于最佳刺激是必需的。