How naive T cells decline with age

Why?

T cells: Function and destiny

T cells are essential for effective immunity and two broad types of cells exist to protect us: Naïve T cells and memory T cells. Naïve T cells are new recruits; they've neither fought nor been exposed to pathogens but are extremely diversified and provide essential cover against new infectious agents. Conversely, memory T cells are less diverse but are veterans; scarred and hardened from fighting malicious invaders. As soon as puberty begins naïve T cells start to gradually disappear, eventually rendering aged individuals more susceptible to infections, particularly from new pathogens that have not triggered memory cells. The prevailing view to explain the loss of naïve T cells is the decline in the production of new T cells in the thymus and a natural, life-long conversion of naïve T cells into memory cells. However, the thymus continues to produce low levels of naïve T cells as we age and T cells have a very long lifespan. So, what's the real reason to explain the loss?

An investigation into the loss of naïve T cells

Charles Surh, director of AIM, and his team have sought to answer this aged question. They looked at the lymph node and found deterioration in the population of stromal cells: Static cells that are essential in supporting the survival of naïve T cells while maintaining the structure of the lymph node. Director Surh explained, "This hypothesis had never been investigated before -- to look whether a defect in the stromal cell population, within the lymph node contributed to naïve T cell loss. This defect must be rectified first before T cells can be replenished."

To investigate the legitimacy of their hypothesis the team set a number of experiments in place. Mice with lower than normal numbers of white blood cells {lymphopenic mice} were tested to see if they had the ability to support a natural proliferation of mature T cells. Previously, the team found this approach to be a sensitive way to measure the factors that support naïve T cell survival. Such factors declined moderately in middle-aged mice and sharply in old mice. The team also delivered extra naïve T cells into old mice, but to no avail. The injected T cells simply dissipated within two weeks in the old mice but persisted much longer in younger mice. The team's hypothesis was looking promising. "It validated our informed suspicions that aging induces changes in the environment that supports T cell survival," commented the amiable director. "Then, we focused our attention on the population of stromal cells in the lymph nodes."

To delve deep into the inner workings of naïve T cell survival it is paramount to study the subset of stromal cells in the lymph nodes that serve to support T cells, namely, the follicular reticular cells (FRCs). In essence the team found naïve T cells failed to effectively migrate into the lymph node and interact with FRCs. This was, according to the team's paper, due to a decline in the production of a chemokine CCR19: A protein produced by endothelial and stromal cells to attract T cells to the lymph nodes to interact with FRCs. Moreover, the FRCs, which exist as a fine network of webbed structures in young mice, were found in lower numbers and highly disorganized in old mice.

Problem solving at AIM

The results strongly supported the team's theory. "Our work is the first to demonstrate that the decrease in naïve T cell numbers in old age is only not due to a decline in their {T cells} production in the thymus but also from deterioration in the environment that supports the survival of these cells," said Director Surh, from AIM's headquarters in Pohang, South Korea. "This is a new concept that has not been considered before, and could be a more relevant factor contributing to naïve T cell loss in old individuals than other previously suggested mechanisms. We hope that our contribution will trigger others to investigate why stromal cells that support naïve T cell survival deteriorate with age, as this will be a difficult question to solve on our own."