Using T cells primed for the infectious disease toxoplasmosis, Whitehead Institute for Biomedical Research researchers have created novel mouse models of the immune system that more accurately reflect how immune cells actually respond to pathogens in their presence.
“These models have a lot of potential,” says Oktay Kirak, who is a postdoctoral researcher in the labs of Whitehead Institute members Hidde Ploegh and Rudolf Jaenisch. “It allows us to study both the biology of T cells as well as their role in toxoplasmosis.”
Toxoplasma gondii, the single-celled parasite that causes toxoplasmosis with more than 30 percent of humans infected, the symptoms are generally minor, although toxoplasmosis can have serious or fatal effects for an immunocompromised person or a fetus, if the mother is infected during pregnancy.
In the April 9 issue of Science, Kirak and his colleagues describe how he used somatic cell nuclear transfer (SCNT) to create mice from single T cells that recognize the Toxoplasma gondii parasite.
In SCNT, a cell’s nucleus is inserted into a de-nucleated, unfertilized egg cell to generate embryonic stem cells and animals with the same genetic code. In this study, Kirak, who is first author of the Science paper, transferred the nucleus of a T cell primed for toxoplasmosis into an enucleated, unfertilized mouse egg to create mice.
Kirak used T cells—a class of white blood cells that include several types of cells including cytotoxic or so-called killer T cells—because they have been difficult to study in current immune system models. Each cytotoxic T cell has its genetic material rearranged, so that it produces properly activated a receptor that can identify an antigen. An antigen is a particular part of an infectious agent, such as a virus, bacterium, or parasite, that the immune system can recognize. Once properly activated by the relevant antigen, the cytotoxic T cell will then kill any cell that is infected with that pathogen.
Many T cells may respond to a particular infectious agent, such as Toxoplasma gondii and they all may recognize different antigens on the parasite’s surface. This multiple-pronged attack, though highly beneficial in eliminating infectious agents, complicates the study of specific T cell’s interactions with the antigen and infectious agent. Kirak’s method solves this problem by creating a mouse with identical T cells and activating them in the course of infection.
