Tyron Chang, PhD

Author Profile

Tyron Chang is a PhD student at the University of Texas Southwestern Medical Center in the Immunology Department.

Prior to graduate school, he studied how Th2 responses can regulate viral latency in murine B cells. Currently, his research focuses on how macronutrients can selectively enhance protein stability to trigger antiviral defense in mammalian cells.

5 blogs authored by Tyron Chang, PhD

Regular Contributor

Qualification

PhD in Biomedical Science

Articles

Training the Immune Mind: Advancing Vaccine Design to Educate T Cells

Training the Immune Mind: Advancing Vaccine Design to Educate T Cells

In this blog, we will discuss the role of T cells in the vaccine-induced immune response and the key challenges in achieving long-lasting and broad-spectrum immunity.

Therapeutic Dilemmas: Exploring the Dual Nature of IL-17 in Immune Responses

Therapeutic Dilemmas: Exploring the Dual Nature of IL-17 in Immune Responses

In this blog, we will discuss the pathological implications associated with IL-17A and current therapeutic treatments for diseases.

Tiny Gut Microbes Boost the Immune System to Fight against Cancer

Tiny Gut Microbes Boost the Immune System to Fight against Cancer

In this blog, we will delve into how the microorganisms residing in our intestines can impact the anti-tumor response triggered by immune checkpoint blockade therapy.

From Powerhouses to Inferno: A Mitochondrial Messenger Fuels Inflammation

From Powerhouses to Inferno: A Mitochondrial Messenger Fuels Inflammation

In this blog, we discuss the concept of immunometabolism, including a new study published by Hooftman et al. (2023) in Nature showing how a molecule derived from mitochondrial metabolism can trigger inflammation, providing insights into the versatile functions of these organelles beyond energy production.

Immune Cells Get an Upgrade: A Stronger Defense against Cancer

Immune Cells Get an Upgrade: A Stronger Defense against Cancer

This blog takes a look at recent advances in CAR T-cell therapies, which allow CAR expression and release of cytokines in a controllable manner.

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