National Institute on Aging grants USD 13M to UoA for research

University of Arizona Health Sciences researchers received a $13.1 million grant from the National Institute on Aging to continue studies aimed at rejuvenating the immune system of older people in order to improve health throughout the lifespan.

Older adults are disproportionally affected by infection, cancer and certain types of autoimmune disease. This is influenced by the fact that as a person ages, their body produces fewer T cells and gets less proficient at maintaining them. T cells are a type of white blood cell essential to the immune system and defense against infection.

“It is clear how much our immune system declines with age when you look at all the previous epidemics and pandemics that have hit us, including Covid-19. Older adults die at a rate somewhere between 50 to 300 times more frequently than people in the younger age groups. We are looking at the thymus gland, which develops T cells, and at the lymph nodes, which maintain them, and examining how we can combat the erosion of age by jumpstarting them.” – Janko Nikolich, MD, PhD, principal investigator, professor and head of the Department of Immunobiology at the University of Arizona College of Medicine – Tucson.

The second project, “Role of the microenvironment in regulating early stages of thymic involution and central tolerance,” is led by Lauren Ehrlich, PhD, professor of molecular biosciences and oncology at the University of Texas at Austin. It will examine how the cellular composition of the thymus changes with age, which could impact the quantity and quality of developing T cells.

The third project, “Peripheral T cell maintenance defects with aging,” focuses on how aging affects the lymph nodes. It is part of Nikolich’s continuing studies of how the decline in naive T cells impacts the immune system. Naive T cells are produced in the thymus but need additional support from the lymph nodes to function effectively.

“Our previous research has shown that defects in the lymph nodes can powerfully undermine the benefits of reawakening T cell production in the thymus,” said Nikolich, who is a member of the university’s BIO5 Institute. “So, even if we can generate a plethora of high-quality T cells, if the lymph nodes are impaired, those T cells will be clueless. They will not be able to quickly react and respond to infection.”

The first signs of age-related vulnerability to infection start between the ages of 40 and 50. More drastic declines in the immune systems are seen in the 60s, 70s and 80s. Nikolich says interventions to improve T cells and the immune system could greatly benefit the quality of life for older people and provide substantial economic relief for health care expenses. University of Arizona Health Sciences