Improving Trauma Survival Hinges on the Body's Own First Responders

By Kara Gavin | | 16 March

improving trauma survival hinges on bodys own first responders

A car crash. A battlefield blast. A bad fall. Traumatic injuries of all kinds claim the lives of nearly 200,000 Americans each year and send 27 million to emergency rooms. The cost: $670 billion.

More people survive these injuries than ever before, thanks to the care they get from first responders and specialized trauma teams.

But a team of scientists argues that to further improve care, more focus should be directed at another team of first responders: the ones that make up the body’s innate immune system.

These tiny cells and proteins react immediately when the body suffers an injury, to fight its effects on tissues and organs and to clear damage.

But these minuscule first responders can also overreact and spiral out of control —leading to death days or weeks after an injury. For those who survive, that overzealous immune response can worsen long-term disability, such as lasting cognitive defects from a traumatic brain injury or loss of limb function.

Writing in Nature Immunology, a trio of scientists examines what prior scientific research has revealed about the intricate nature of response and overresponse.

Their conclusion: It’s time for the immunology and trauma communities to work more closely together to translate new knowledge into better patient care.


Lessons From Sepsis Care

Peter A. Ward, MD, the senior author of the new review article and a pathologist at the University of Michigan, hopes the analysis will prompt similar response to what has happened in the field of sepsis.

Survival from that syndrome, in which the body’s immune response to infection turns into a disastrous inability to control the inflammatory responses body-wide, has improved in recent years.

Ward attributes those gains to better awareness of the clinical problem among providers and the public, and to evidence-based supportive care that helps tamp down the inappropriate immune response while boosting other functions and supporting failed organs such as the lungs.

But he also notes that studies have shown sepsis survivors still have a much higher risk of dying after “recovery” than people similar to them who didn’t battle sepsis. The long-term effects of living through a massively overzealous immune response are still being studied.

The same thing appears to be happening in trauma, says Ward, the former chair of the Department of Pathology at the U-M Medical School. Rapid and advanced trauma care saves the patient from immediate death, but patients still die of complications or live with long-term effects on their brains and organs.

“Post-trauma sepsis is very similar to traditional patterns of infectious sepsis, though the triggers are different,” Ward says. “We need to identify the extent to which some of the approaches that work in sepsis could work in trauma and protect against progression of inflammation.”


Dr. Peter Ward
"We need to identify the extent to which some of the approaches that work in sepsis could work in trauma and protect against progression of inflammation."Peter A. Ward, M.D.


A Complex Chain Reaction

The new paper summarizes dozens of findings from basic research laboratories that study the immune response to trauma — including some made by Ward and first author Markus Huber-Lang, director of the Institute for Clinical and Experimental Trauma-Immunology at University Hospital in Ulm, Germany. Huber-Lang trained in Ward’s lab two decades ago during the early days of understanding immune response in sepsis.

“We found then that a strong driving force of the adverse effects of sepsis was the complement system, which consists of the pro-inflammatory factors that contribute to the multi-organ dysfunction seen in sepsis,” Ward notes. “We now know that in trauma, no matter what the starting location is in the body, the insult triggers activation of the same cell types, which start to produce the same pro-inflammatory factors.”

For the new paper, the authors gathered evidence from studies of trauma to three common sites: the head, chest and abdomen.

The effects of trauma on the brain, lungs and gut — and the immune response to each kind of trauma — differ greatly.

But the bottom line for all is that the release of “distress-signal” proteins (called cytokines, chemokines and other “danger signals”) by first-responder immune cells can quickly overwhelm the ability of other immune system cells to clear the debris.

And that can cause those “cleanup” immune cells, such as T cells and B cells, macrophages and monocytes to shut down or even die — which means even fewer cells to respond to the microscopic cries for help coming from the trauma site. The distress-signal molecules also encourage clot formation, which can help stop blood hemorrhage but can also clog vessels and cause more damage.

“Responses that ordinarily are quite contained and limited, and will usually fade gradually, don’t diminish, which results in a spiraling cycle of overwhelming response,” says Ward. That can lead to direct damage to organs nearby or even ones far from the site of the injury.

Plus, other factors can make things even worse, such as infectious bacteria that can invade a body through broken skin, the insult of undergoing repeated operations to repair broken bones and torn tissues, medications that disrupt the body’s natural population of helpful microbes, and any underlying health issues the person had before getting injured.


Effects on Immune Response

The long-term effects of trauma and sepsis often include a reduced overall immune response, or immunosuppression, because T cells and B cells can’t be replaced once they’ve died. This can put survivors at risk of repeat infection and more, collectively referred to as “immune-suppression.”

Ward notes that research has not yet shown how to reverse this weakened state, although scientists are looking for options in the lab using animal models.

Another approach to balancing the innate immune response to trauma is to block the distress-signal molecules produced by the complement immune system. But the risk of going too far and interfering with lifesaving pathways that allow the body’s phagocyte cells to vacuum up infected or damaged cells is very real.

Clinical trials are also in the works to test drugs or antibodies that can inhibit pro-inflammatory proteins produced by the complement system, called C5A, that Ward and others have studied in detail. Some of Ward’s and Huber-Lang’s past work, patented by U-M, has been licensed to a company exploring such options.

“Testing these approaches will be quite tricky, and the clinical trials will need to be carefully crafted,” says Ward. But now that the system for immediately responding to traumatic injury and fixing its immediate effects is well-organized, the next frontier for improving trauma care lies within our bodies, in the complexities of the innate immune system.