Smarter Treatment for Killer Infections

Released: 5/11/2011 3:00 PM EDT
Embargo expired: 5/12/2011 12:00 PM EDT
Source Newsroom: Case Western Reserve University
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Citations Immunity

Newswise — Sepsis is a major killer in hospital intensive care units. Researchers at Case Western Reserve University School of Medicine have found that manipulating a genetic factor that can launch or throttle the body’s defenses can improve survival rates during bacterial infection.

“Currently, our therapies for sepsis are very limited,” said Mukesh K. Jain, MD, Ellery Sedgwick Jr. Chair, director of the Case Cardiovascular Research Institute, and professor of medicine at Case Western Reserve University School of Medicine and chief research officer of the Harrington-McLaughlin Heart & Vascular Institute at University Hospitals Case Medical Center.

Lead author Ganapati H. Mahabaleshwar, PhD, assistant professor of medicine at Case Western Reserve School of Medicine spearheaded the effort, which included researchers from St. James Hospital, Dublin, Ireland; and the University of Cincinnati College of Medicine. They discovered that indiscriminately boosting immune cells may cause harm and even death. Surprisingly, when a patient is suffering from the end-stage of sepsis, the defense system needs to be curbed to prevent the body’s own immune cells from contributing to shock and death.

The work is published in the May 27 edition of the journal Immunity.

The key to better sepsis therapies is knowing when to turn up or turn down the factor, called Kruppel-like transcription factor 2, or KLF2 for short, says Dr. Jain, the senior author of the study.

Inside immune cells called macrophages, KLF2 acts like a concert mix-master. But, instead of adjusting the base and feedback, the factor adjusts cell activities according to signals from the internal environment.

Normally, the factor maintains immune cells in a quiet state. But during the first phase of sepsis, when bacteria begin to attack, the resulting low oxygen levels and high amounts of bacterial products cause the level of KLF2 to be reduced.

The reduction in KLF2 essentially opens the gates for macrophages to release noxious products that kill bacteria, the investigators found.

But when sepsis moves into the second phase, marked by low body temperature and blood pressure, tissue damage, and a cascade of organ shutdowns, the body’s own defenses are doing harm by promoting inflammation that can cause shock and death.

“In this phase, it’s time to boost KLF2 and quell unbridled inflammation,” Dr. Jain says.

The body, however, does not do this naturally. The researchers don’t know why but suspect that continued hypoxia and leaching of bacterial products into circulation keep KLF2 levels low.

The research builds on the Jain lab’s 2006 discovery of KLF2 in macrophages. In the new study, testing showed that mouse models deficient in KLF2 were effective in defeating polymicrobial infections in the early stage of infection. But, in testing the late-stage of sepsis, mouse models lacking KLF2 were more likely to die and die sooner.

Testing of blood samples taken from hospital patients suffering from sepsis produced the same patterns.

The team is now looking for compounds that could reduce the amount of KLF2 in the first phase of infection, and other compounds to bolster levels in the second phase.

Dr. Jain’s group as well as other researchers have found that statins, the class of drugs used to reduce cholesterol levels, and resveratrol, the substance in red wine credited with boosting good cholesterol, may be useful in combating sepsis. Dr. Jain’s team suggests that the timing of administration of such therapies may determine how patients respond to sepsis.

About Case Western Reserve University School of Medicine
Founded in 1843, Case Western Reserve University School of Medicine is the largest medical research institution in Ohio and is among the nation’s top medical schools for research funding from the National Institutes of Health. The School of Medicine is recognized throughout the international medical community for outstanding achievements in teaching. The School’s innovative and pioneering Western Reserve2 curriculum interweaves four themes--research and scholarship, clinical mastery, leadership, and civic professionalism--to prepare students for the practice of evidence-based medicine in the rapidly changing health care environment of the 21st century. Nine Nobel Laureates have been affiliated with the school of medicine.

Annually, the School of Medicine trains more than 800 MD and MD/PhD students and ranks in the top 25 among U.S. research-oriented medical schools as designated by U.S. News & World Report “Guide to Graduate Education.”

The School of Medicine’s primary affiliate is University Hospitals Case Medical Center and is additionally affiliated with MetroHealth Medical Center, the Louis Stokes Cleveland Department of Veterans Affairs Medical Center, and the Cleveland Clinic, with which it established the Cleveland Clinic Lerner College of Medicine of Case Western Reserve University in 2002. http://casemed.case.edu.


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