Skip to main content
News Franklin 04.2022
© Franklin Lab / Uni Bonn

News categories: Publication

New approach against chronic inflammation

ASC-specks in mice targeted with nanobodies

Researchers of ImmunoSensation2 at the Universities of Bonn together with colleagues at the University of Sao Paulo have succeeded in mitigating chronic inflammation in mice using customized "mini-antibodies". These nanobodies enabled them to dissolve molecular complexes in tissue that normally activate the immune system. The nanobodies produced may in future help to slow down unwanted inflammatory reactions that cause diseases such as arthritis or neurodegeneration. The study is published in the journal EMBO Molecular Medicine.

The cells in our body have a sophisticated alarm system, the inflammasome. Its central component is the so-called ASC protein. In the event of danger, such as an attack by a pathogen, many of these molecules join together to form a large complex, the ASC speck. This ensures two things: First, its activity causes the cell to accumulate large quantities of messenger substances, which can be used to summon the help of the immune system. And secondly, numerous pores are formed in the cell membrane through which these alarm molecules can reach the outside and fulfill their task.

Last cry for help from the dying cell

These holes ultimately lead to the demise of the cell: "At some point, the cell basically explodes and empties its entire contents into the tissue," explains Cluster member Prof. Dr. Bernardo Franklin of the Institute of Innate Immunity at the University Hospital Bonn. "The messenger substances that are now abruptly released then act like a last great cry for help. This triggers the immune system to mount a strong inflammatory response that contains the infection." That is why this mechanism of innate immune defense is hugely important.

However, in this process, ASC specks also accumulate in the tissue and may persist there for a long time. "We have now been able to show in mice that their activity activates the immune system, even after the threat has been averted," Franklin says. "This can result in chronic inflammation, which severely damages the tissue." Together with researchers from the University of Sao Paulo, Franklin's team has succeeded in preventing this undesirable effect. They used so-called nanobodies for this purpose.

These agents are antibody fragments with a very simple structure. "In collaboration with Prof. Dr. Florian Schmidt from the Institute of Innate Immunity, we generated nanobodies that specifically target ASC and can dissolve the specks," explains Franklin's collaborator Dr. Damien Bertheloot. The researchers got help from an alpaca: They injected the animal with the ASC protein so that it developed matching antibodies. Some of the alpaca antibodies have a very simple structure. This makes it possible to produce and test fragments of these antibodies as so-called nanobodies.

Rheumatism and gout symptoms alleviated in mice

The researchers were able to obtain the genetic information for the ASC nanobodies from blood samples of the animal using a complex technique. "We then incorporated this genetic makeup into bacteria so that we could have them produce the nanobody in large quantities," Bertheloot explains. The team demonstrated that the compound can dissolve ASC specks using human cell cultures as well as mice. "The mice in our experiments have rheumatoid and gout-like symptoms," Bertheloot explains. "After administration of the nanobody, the inflammation and also the general health of the rodents improved significantly."

Nanobodies are very small compared to normal antibodies. They are therefore excellent for breaking up such molecular complexes. This is because they can still reach sites that would be too cramped for large agents. Moreover, normal antibodies provide additional stimulation to the immune system and can therefore exacerbate inflammation - a property that nanobodies lack.

The results are also interesting for another reason: Studies indicate that ASC specks can also cause significant damage to the brain. There, they seem to serve as a kind of "crystallization nucleus" for the Aß protein. In the brains of Alzheimer's patients, Aß clumps together to form large protein complexes called plaques. Presumably, ASC specks can trigger this clumping. "So perhaps it's possible to slow down this process with the help of our nanobodies," Franklin hopes. "We now plan to investigate this possibility in a follow-up study."

At the same time, however, he warns against overly high expectations: Even in the ideal case, it will be years before the results might translate into new drugs.


Participating institutions

The Institute of Innate Immunity and the Nanobody Core Facility at the University Hospital Bonn were involved in the study. Partners on the part of the University of Sao Paulo were the Center for the Study of Inflammatory Diseases and the Department of Pharmacology.

Publication

Damien Bertheloot et al.: Nanobodies dismantle post-pyroptotic ASC specks and counteract inflammation in vivo; EMBO Molecular Medicine; DOI: https://doi.org/10.15252/emmm.202115415


Contact

Prof. Dr. Bernardo S Franklin

Institute of Innate Immunity

University Hospital Bonn

Phone: +49 228/287-51981

Email: franklin@uni-bonn.de

Lead author Damien Bertheloot and his publication are featured in Episode #2 of Spot on Science

Related news

News Icon

News categories: Publication

New insights into the human immune defense against poxviruses

An international research team involving Bonn scientist has made an important contribution to understanding the human immune response to poxviruses: The scientists were able to show for the first time that different human cell types recognize poxviruses via different sensors in order to trigger inflammatory responses. At the same time, the team developed the world's first nanobodies that can specifically block the DNA sensor AIM2 – a tool that opens up new possibilities for inflammation and infection research. The paper has now been published in The EMBO Journal.
View entry
News Icon

News categories: Publication

Multiple Sclerosis: Potential biomarker linked to progression and brain inflammation identified

Better ways to detect ongoing brain damage in multiple sclerosis (MS) are urgently needed. An international team of scientists, including ImmunoSensation³ member Prof. Anne-Katrin Pröbstel, has identified a molecular circuit that drives brain injury in MS. In a mouse model, blocking the enzyme Bruton's tyrosine kinase prevented harmful clustering of immune cell and brain tissue demage. Patient data revealed the same immune signaling pattern, suggesting strong translational potential for diagnosis. The study was recently published in Nature Immunology.
Full publication
Symbol Image

News categories: Publication

Instructions for building antibodies decoded

MOG Antibody-associated Disease (MOGAD) is a rare autoimmune disease of the central nervous system. The blood of patients contains antibodies against myelin oligodendrocyte glycoprotein (MOG), a protein in the myelin layer that surrounds the neurons in the brain. It is believed that these antibodies contribute to the destruction of this protective layer in the brain. Researchers at the University Hospital Bonn (UKB) and the Universities of Basel and Bonn, in collaboration with an international team, have now deciphered the construction plan of the anti-MOG antibodies.
View entry

Back to the news overview