Neurons are poorly recognized by the immune system which contributes to the ability of neurotropic pathogens to persist in the CNS but there is evidence that T cells can promote clearance of these organisms. For the parasite Toxoplasma gondii, T cell production of the cytokine IFN-? is important for resistance in the CNS because it activates hematopoietic and non-hematopoietic cells to control the tachyzoite (lytic) stage of the infection. Conversely, in response to cellular stress T. gondii transforms to the latent bradyzoite stage and forms long lived cysts in neurons. The lack of therapies that target the latent stage of T. gondii is a significant impediment to the management of this infection. Current dogma holds that because this stage is in neurons it evades immune surveillance and ensures chronicity. However, there is accumulating evidence of a more active battle between the host and parasite in the CNS. These observations indicate that T cell production of IFN-? activates neurons to control T. gondii but the ability of this parasite to persist may be because bradyzoites evade recognition and/or modulate cyst specific responses. In support of this idea, comparisons between tachyzoite and bradyzoite specific responses suggest that cyst-specific CD8+ T cells have reduced effector functions. To understand how T. gondii is recognized in neurons and how the parasite can evade surveillance, novel transgenic reporter systems for parasites will be combined with host reporters to track the fate of infected neurons in vivo. Additional studies will determine the impact of IFN-? on neurons and live imaging studies will visualize interactions between T cells and infected neurons and if this results in parasite clearance or evasion of T cell activities. The findings that emerge from these studies will have a significant impact on understanding how CD8+ T cell-neuron interactions lead to pathogen control and will be relevant to other neurotropic infections and neuroinflammatory conditions.
Neurons are poorly recognized by the immune system which contributes to the ability of neurotropic pathogens to persist in the CNS. However, there is evidence that T cells can promote clearance of these organisms from neurons, but the basis for this activity is not well understood. The parasite Toxoplasma gondii, has a latent cyst forms that survives in neurons which helps it evade immune surveillance and ensures chronicity. There is a dire need for new therapies for this latent stage. To understand how T. gondii is recognized in neurons and how the parasite can evade surveillance, novel reporter systems for parasites will be used to track the fate of infected neurons in vivo and studies performed to determine if cyst specific responses can help eradicate this pathogen. These studies will have a significant impact on understanding how CD8+ T cell-neuron interactions lead to pathogen control and be relevant to other neurotropic infections.
