The role of HOX 4 paralog genes in maintenance and expansion of T memory cells

我们的免疫细胞在体内巡逻，以检测和应对外部入侵者，如细菌和病毒。一旦他们清除了攻击，一些免疫细胞将被保留数年，使我们能够更有效地对同一入侵者进行第二次攻击。我们将这些细胞称为免疫记忆。记忆细胞有两类，B细胞型(主要参与细菌感染)和T细胞型(主要参与病毒感染)。记忆细胞的数量很少，为了防止它们在反复遇到入侵者时成熟为效应免疫细胞而丢失，这些细胞偶尔会分裂成两个子细胞，其中至少一个与原始细胞完全相同。更稀有的血液干细胞也会经历这种自我更新的分裂，以保持自己的数量，从而提供终身的血液供应。目前的想法是，决定自我更新分裂的分子在两种细胞类型中是相同的。我们有兴趣了解如何扩大T存储单元池。HOXB4蛋白已知可以增加血液干细胞的数量，因此我们假设这种蛋白也可以扩大记忆细胞。我们的第一个结果确实表明，在HOXB4存在的情况下，T存储单元子集的扩展确实比对照更好。我们想用小鼠来测试这些扩大的记忆细胞是否能产生免疫反应。此外，还将用HOXB4在细胞培养和小鼠体内测试其他记忆细胞亚群的扩增情况。最后，我们将研究HOX基因和最近被证明在记忆T细胞中重要的其他分子(Wnt)之间的关系。

Our immune cells patrol the body to detect and respond to external invaders, such as bacteria's and viruses. Once they have cleared the attack, a few immune cells will be kept for years, enabling us to act more efficiently in second attack of the same intruder. We refer to these cells as immunological memory. There are two classes of memory cells, those of the B-cell type (predominantly involved in bacterial infections) and of the T-cell type (predominantly involved in viral infections). The number of memory cells is very low, and to prevent their loss, due to maturation into effector immune cells upon repeated encounter with the intruder, these cells divide occasionally into two daughter cells of which at least one is exactly the same as the original cell. Blood stem cells, which are even rarer, undergo as well this type of self-renewal divisions to maintain their numbers, enabling to provide a life-time blood supply. The current thought is that molecules determining the self-renewal divisions are the same in both cell types. We are interested in understanding how to expand the T memory cell pool. The protein Hoxb4 is known to increase the blood stem cell numbers, and thus we hypothesized that this protein can expand memory cells as well. Our first results show indeed a better expansion of a T memory cell subset in the presence of Hoxb4 than control. Using mice we want to test whether these expanded memory cells can produce an immune response. Furthermore, other memory cell subsets will be tested for expansion with Hoxb4 in cell culture and in a mouse. Finally, we will investigate the relation between Hox genes and other molecules (Wnt) that have recently been shown to be important in memory T cells.