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A model for the immune system and inflammation, perhaps even COVID
ORLANDO, Fla.—Hesperos Inc. recently announced the publication of a new peer-reviewed publication that describes how the company’s technology can be used to investigate immune responses following treatment with biological therapeutics for multi-organ systemic diseases, including cancer, infectious diseases and inflammatory disorders.
The study titled “Differential Monocyte Actuation in a Three-Organ Functional Innate Immune System-on-a-Chip “ was part of a collaboration between Hesperos, Hoffman-La Roche Pharmaceuticals and the University of Central Florida and appeared in the journal Advanced Science.
As the company explains, the immune system plays an important role in coordinating with other organ systems to combat infection, eliminate damaged cells and repair tissue. However, modeling immune response following drug treatment in preclinical studies is challenging due to poor predictability, especially for the innate portion of the system. As the scientific community continues to move toward greater use of multi-organ, human-on-a-chip systems as a cost-effective way to increase efficiency and lower toxicity, it has been noted many of these models lack a systemic immune component.
In the study, researchers describe an in-vitro, pumpless, three-organ system containing functional human cardiomyocytes, skeletal muscle and hepatocytes in a serum-free medium, along with recirculating human monocyte THP-1 immune cells. Monocytes are a vital immune system cells involved in wound healing, pathogen clearance and activation of the innate immune response, Hesperos points out, but are also responsible for the cytokine storm found in conditions such as sepsis.
“One application where the immune-system-on-a-chip can be immediately useful is for uncovering how severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) directly affects multi-organ systems by activating the cytokine storm from inflammatory macrophages and to support the rapid development of therapeutics,” said Dr. Michael L. Shuler, CEO of Hesperos. “As the global pandemic of COVID-19 continues to grow, this system has the potential to quickly evaluate antiviral and repurposed drugs to help combat this devastating disease.”
In the study, the researchers evaluated two different innate immune responses: (1) targeted immune response following tissue-specific damage, which simulates indirect activation of THP-1 cells and (2) pro-inflammatory immune response following direct activation of immune cells, mimicking acute inflammation and the cytokine storm. Though not reported in this study, Hesperos has previously shown that peripheral blood mononuclear cells and T cells are sustainable in these multi-organs systems, which would allow some aspects of adaptive immunity to also be modeled.
In the targeted immune response experiments, the cardiotoxic compound amiodarone was used to selectively damage cardiac cells to evaluate how THP-1 immune cells affect the three-organ system. The presence of both amiodarone and THP-1 immune cells led to a more pronounced reduction in cardiac force, conduction velocity and beat frequency compared to amiodarone alone. THP-1 cells were also found to infiltrate the damaged cardiomyocytes and induce significantly increased cytokine IL-6 expression, indicating an M2 macrophage phenotype. No immune-activated damage was reported in the skeletal muscle or liver cells.
“The most striking features of our immune-system-on-a-chip is that it emulates different immune reactions for direct tissue-damage and acute inflammation, as well as distinguishes between M1 vs. M2 macrophage phenotypes,” said Dr. James Hickman, chief scientist at Hesperos and a professor at the University of Central Florida.
The study was initially funded by Roche Pharmaceuticals and completed under an NIH grant from National Center for Advancing Translational Sciences’ (NCATS) Small Business Innovation Research program, which supports studies to advance tissue chip technology toward commercialization.
“Tissue chips are a promising technology for accelerating the preclinical timeline and getting treatments to patients more efficiently,” said Dr. Danilo A. Tagle, associate director for special initiatives at NCATS. “Finding improved ways to study immune responses has tremendous implications for drug discovery and the development of more effective personalized medicines in diseases that affect multiple organ systems.”
In the pro-inflammatory response experiments, the three-organ system was exposed to lipopolysaccharide (LPS) and interferon gamma (IFN-γ) to stimulate acute inflammation/cytokine storm and provoke monocyte differentiation and activation. In the absence of THP-1 immune cells, LPS/ IFN-γ treatment had no significant effect on function of the three-organ system. However, with the addition of THP-1 immune cells, LPS/ IFN-γ treatment caused cellular damage to all three-organ components, including THP-1 cell infiltration in liver tissue, and led to significant alterations in cardiac force and beat frequency, as well as skeletal muscle force.
To read the full manuscript, visit https://doi.org/10.1002/advs.202000323.