Insects are ubiquitous, diverse, and able to combat infections despite their lack of adaptive immunity. Insects have a robust innate immune system that is divided into two branches, cell-mediated and humoral. Activation of cell-mediated immune responses results in phagocytosis, nodule formation, and encapsulation by the insect’s immune cells, hemocytes. Activation of humoral immunity results in the production of anti-microbial peptides (AMPs) and phenoloxidase (PO). Insect immune responses can be plastic with development. However, research on how and why insect immunity changes with age as insects develop within a larval developmental stage (instar) is limited and contradictory. In my dissertation research, I answer two main questions: 1) how do immune responses vary within an instar and 2) what drives changes in immunity within an instar? My dissertation research showed that humoral immune responses are more robust at the beginning of the 5th and final instar in Manduca sexta (tobacco hornworm) compared to responses from animals later within that instar. Many changes occur within an instar that could affect immunity. For example, I found that protein expression of matrix metalloproteinase (MMP) in immune tissues of M. sexta decreases throughout the 5th instar. Though MMPs are involved in immune responses in other insects, MMP was not found to be immunostimulatory in M. sexta. Another important factor that changes within an instar is the level of juvenile hormone (JH). JH, a developmental hormone that prevents early molting, peaks early and decreases within an instar until molting. I determined that JH is necessary to survive an infection, control bacterial growth in hemolymph (insect blood), and mount an AMP activity immune response. My dissertation research has established that there is a development-immunity link, and that the naturally fluctuating levels of JH may mediate the effect of development on immunity.