Drugs that help treat infectious diseases are known collectively as antimicrobials. They include antibiotics, which target bacteria like E. coli, antivirals to treat viruses like HIV, antifungal medications for fungi like athlete’s foot, and antiparasitics for parasites like pinworm. People who are immunocompromised, like those with primary immunodeficiency (PI), rely on antimicrobials more than the general public because their immune systems are less capable of fighting infections alone. In fact, antimicrobial prophylaxis, in which antimicrobials are used to prevent infections in the first place, is the standard of care for PIs like chronic granulomatous disease (CGD).
Collectively, antimicrobials revolutionized medicine in the 20th century, lowering the mortality rates for all kinds of infectious diseases. However, as the use of antimicrobials rose, antimicrobial resistance emerged as well.
Antimicrobial resistance describes the failure of a particular drug to treat an infection it used to be effective against. When someone has an infection that is resistant, it is the germs, or microorganisms, themselves that ‘resist’ the drug, not the patient’s body. For example, methicillin-resistant Staphylococcus aureus (MRSA) is a strain of staph bacteria that is no longer killed by the antibiotic methicillin (or by related antibiotics like amoxicillin or cephalosporins). One paper estimated that 1.27 million deaths in 2019 were the result of bacterial infections resistant to antibiotics.
Microorganisms that become resistant to antimicrobials have changed genetically over time so that they are less and less affected by a particular drug or class of drugs. Antimicrobial resistance is essentially an evolutionary survival mechanism, so resistant microorganisms usually develop soon after the antimicrobial becomes widely used. In the case of staph, MRSA was first detected in 1961, about a year after methicillin became widely used to treat staph infections.
Some strains of microorganisms, like extensively drug-resistant tuberculosis (XDR TB), have accumulated resistance to not just one, but several chemically unrelated drugs. People who contract XDR TB or other multidrug-resistant microorganisms have few options to treat their infections. Although such an infection has not yet been documented, the nightmare scenario of a ‘superbug’ that is resistant to all drugs typically used to treat it is a very real possibility.
Using antimicrobials only when necessary and only when they will be effective is key to stopping the development and spread of antimicrobial resistance. Responsible antimicrobial use, also known as antimicrobial stewardship, involves many players in healthcare, from individual doctors and patients to entire hospital systems. Examples of antimicrobial stewardship include:
IDF works with policymakers to address antimicrobial resistance by pushing for policies that promote systemic antimicrobial stewardship.
Because antimicrobial resistance is so widespread for some drugs, research to find new antimicrobial drugs is very important. However, many pharmaceutical companies have abandoned antimicrobial research in pursuit of more profitable drugs, and innovative ideas are needed to combat these market challenges. For example, the Pioneering Antimicrobial Subscriptions to End Upsurging Resistance (PASTUER) Act, originally introduced in 2020, proposes mechanisms that would decouple a company’s profits from the volume of prescriptions for a new antimicrobial.
In addition to supporting policies that promote responsible antimicrobial use, IDF also supports funding and incentives for research to discover and test new antimicrobial drugs.
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