One of the biggest problems in the current world is drug resistance, which affects people all over the world. Researchers looked for strategies to combat drug resistance. One of the key conclusions from a recent study on drug resistance was that how to train the body’s own cells to combat antibiotic resistance. This could help us in reducing drug resistance.
Drug-resistant superbugs have threatened human health for decades. The situation is getting worse because of the shortage of new antibiotics. But what if we changed the way we aim to treat them, and trained our cells to kill these invaders instead of relying on antibiotics to do the dirty work? This new strategy, called host-targeted defence, could help to solve the antibiotic resistance problem.
Antibiotic resistance is a growing concern for global health. A recent report commissioned by the British government shows that every year globally, around 700,000 people die due to infections caused by drug-resistant bacteria. The report also warned that, without action, the death toll could rise to 10 million globally and cost the US$80 trillion to the global economy.
Drug resistance is a serious problem in the United States too. More than 23,000 people die every year due to multidrug-resistant pathogens, which cost the country around $55 billion per year. The main culprits threatening the U.S. are methicillin-resistant Staphylococcus aureus (MRSA), carbapenem-resistant Enterobacteriaceae (CRE) and Clostridium difficile.
The shortage of new antibacterial drugs in development to tackle the growing threat is a disturbing trend. A pathogen that is resistant to a drug reserved to treat infections when all others have failed is a particular concern. This is the case with carbapenem-resistant pathogens.
The decline in antibacterial drugs coupled with the emergence of drug-resistant pathogens demands alternative approaches.
In Malay Haldar’s lab, along with other projects, my colleagues and I are studying how factors in an animal host play a role in response to infections. To test the approach, we are doing this work using a mouse model of infections. Our aim is to find novel traits or factors of the host that can be targeted to boost an individual’s immune response high enough to kill the offending microbes. The host factor we are investigating is called Spi-C, a gene found in every cell of the human body.
Targeting host factors
My interest in host factors arose during my graduate studies. While working on my PhD research project, I learned that host factors, a variety of traits intrinsic to humans, play a significant role in bacterial infections. This inspired me to investigate how the host’s immune system fights bacteria.
New insights into the host’s defence against pathogens have led researchers to explore a new strategy called host-directed therapy (HDT), a relatively recent idea that has only been around for about a decade.
The goal of HDT is to enhance and amplify the host’s immune response to kill pathogens, rather than relying exclusively on antibacterial drugs. By targeting host factors as well as delivering antibiotic treatment, HDTs deliver a double whammy.
The body naturally responds to infections with inflammation, a process in which specific populations of immune cells attack and kill the invading bacteria by either eating them or zapping them with protein weapons. However, uncontrolled inflammation triggers the production of proteins that can cause multi-organ failure and can even kill the host. Therefore, controlling inflammation is crucial to combat pathogens as well as to protect the body from hyperinflammation.
HDTs include a suite of treatments that boost the host’s response to pathogens and also protect the host from the exaggerated immune response. HDTs include cellular therapy, in which a specific population of bone marrow cells is injected into the host body to prevent excessive immune response and tissue injury. Another HDT involves commonly used drugs for noninfectious diseases. Statins and ibuprofen, for example, calm the host’s response to infections. Biologics, the complex molecule drugs produced by recombinant DNA technology, do this too by neutralizing small-sized proteins and reducing tissue damage. Nutritional products, such as vitamin D3, have also been shown to cause a host’s immune cells to release antibacterial substances that enhance pathogen killing.
HDTs in conjunction with antibacterial drugs show great promise in treating various multidrug-resistant pathogens, notably Mycobacterium tuberculosis, the pathogen that causes tuberculosis, one of the top 10 causes of death worldwide.
Personalizing treatments for infections
In the last decade, researchers have made much progress in host factor research, leading to new therapeutic strategies.
One of them is personalized medicine, in which a genomic blueprint can determine an individual’s unique susceptibilities to diseases and choose appropriate therapies.
This concept is applied to noninfectious diseases like cancer. However, the application of the concept in infectious disease is very recent. Nonetheless, personalized medicine leads us to speculate why some individuals are more prone to infections than others. My colleagues and I believe that such differences may be caused by subtle differences in the DNA of the host factor genes. By connecting these differences, called polymorphisms, to the level of individuals’ vulnerability to infections, we hope that our research will contribute to the precision medicine of bacterial infections.
Our quest for a novel host factor
My colleagues in the Haldar lab and I are exploring the role of Spi-C in bacterial infection. Spi-C is essential for the development of a specific type population of cells in the spleen that regulate iron storage in the body. Iron is essential for transporting oxygen in red blood cells.
But, during infections, bacteria also require iron. They need it for growth, and they compete with the host to get it. Hence, if we could alter the activity of the Spi-C gene, we might be able to deprive bacteria of this vital nutrient and thus stop the infections without harming the host.
In a recent paper, we summarized the effect of iron in host cells and its interactions with host factors in the presence or absence of infections.
In mice, we tested the role of the host factor, Spi-C, as a way to defend the host. In this study, we injected a chemical that is a component of the bacteria into the mice. We wanted to trigger changes that occur in the animal during a real bacterial infection.
Our preliminary results showed that the host factor is active in various organs of the mice treated with the chemical. We believe this activation plays a role in host defence. And indeed, we found that losing Spi-C activity increased the release of small-sized proteins that facilitate the host’s defence against pathogens compared to cells that have normal Spi-C activity. We believe this change in small-sized proteins might protect the host from hyper-inflammatory responses in response to infection.
We believe that shifting our thinking from pathogen-targeted therapy to host-directed therapy ushers in a new avenue of precision medicine, which could help to end the drug resistance crisis.
How to train the body’s own cells to combat antibiotic resistance
The present article, how to train the body’s own cells to combat antibiotic resistance, written by Zahidul Alam, Postdoctoral Fellow, University of Pennsylvania, was originally published at The Conversation and republished here at healthy life, with all credit to The Conversation.
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