Graduate Studies

 

First Advisor

Jay Reddy

Degree Name

Doctor of Philosophy (Ph.D.)

Department

Integrative Biomedical Sciences

Date of this Version

12-11-2024

Document Type

Dissertation

Citation

A dissertation presented to the faculty of the Graduate College at the University of nebraska in partial fulfillment of requirements for the degree of Doctor of Philosophy

Major: Educational Studies (Educational Leadership and Higher Education)

Under the supervision of Professor Deryl K. Hatch-Tocaimaza

Lincoln, Nebraska, February 2020

Comments

Copyright 2024, the author. Used by permission

Abstract

Myocarditis patients can chronically develop dilated cardiomyopathy and autoreactive T cells could contribute to the disease pathogenesis, but defining their antigen specificity remains a major challenge. To fill this gap, we generated T cell receptor (TCR) transgenic (Tg) mice specific to cardiac myosin heavy chain (Myhc)-α 334–352 and made a few observations. First, we unexpectedly noted both CD4 and CD8 T cells expressing TCRs specific to Myhc-α 334–352. Second, while Tg T cells from myocarditis-resistant C57BL/6J mice did not respond to Myhc-α 334–352, those from immunized mice responded, indicating that in vivo priming is necessary to break tolerance. Third, upon backcrossing Tg mice onto A/J background for four generations, both CD4 and CD8 T cells from naïve mice responded to Myhc-α 334–352 and produced inflammatory cytokines. Fourth, we noted that CD4 T cells exhibited markers of cytotoxicity similar to CD8 T cells. Fifth, although naïve Tg A/J mice did not develop myocarditis spontaneously, fully backcrossed mice could develop the disease. Finally, we studied the development of myocarditis in diversity outbred mice that may have translational significance because their genetic diversity is relatable to the outbred human population. Overall, the availability of various models we have developed are helpful tools to investigate the roles of autoreactive T cell antigens specifically.

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