NIH-funded research R21 grant

How Candida albicans withstands the immune system's oxidative attack

Official title: Candida albicans Target of Rapamycin in oxidative stress responses

Funded at Boston Children's Hospital · NIH-11237093 · Data updated 2026-11-12

This project is learning whether a specific part of the Candida albicans Tor1 protein helps the fungus survive the immune system's oxidative defenses, with the goal of guiding new antifungal strategies for people with Candida infections.

Quick facts

Grant typeR21 grant
Study typeNIH-funded research
Funding institutionBoston Children's Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startNovember 22, 2024
Project endOctober 31, 2026
Funding year2026
Award (this year)$222,500
NIH project number5R21AI178693-02
Project IDNIH-11237093 on NIH RePORTER

Who could benefit from this research

Could help

Patients most likely to benefit in the future are those with recurrent, mucosal, or invasive Candida infections who need better treatment options.

Less likely to help

People without Candida infections or those with infections caused by other organisms are unlikely to benefit directly from this basic laboratory research in the near term.

What this research studies

From a patient's perspective, researchers are examining a protein in the common fungus Candida albicans called Tor1, focusing on a region known as the N-terminal HEAT repeats. They will use engineered fungal mutants and laboratory experiments to see how this region helps the fungus manage oxidative stress produced by immune cells. The team will measure fungal stress-response systems and metabolic outputs and map physical interactions between Tor1 and redox-related enzymes. All work is done in the lab with fungal cells and molecular methods to identify fungal-specific vulnerabilities.

Why it matters

Potential benefit: If successful, the work could reveal fungus-specific targets that lead to new antifungal drugs or therapies for people with Candida infections.

How similar studies have gone: Prior research has linked TOR signaling to stress responses in fungi, but focusing on the N-terminal HEAT repeats of Candida Tor1 and their unique interactions is a novel and less-explored approach.

Where this research is happening

  • Boston Children's Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Koehler, Julia R — Boston Children's Hospital
  • Study coordinator: Koehler, Julia R

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.