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Characterizing Patient Immune Responses to Emerging Tick-borne Virus

Using patient samples, Dr. Jung and his team uncovered inflammatory biomarkers associated with severe disease and death caused by SFTSV infection, and identified the critical role B cells play in infection.

03/02/2021

Researchers led by Jae Jung, PhD, director of Cleveland Clinic’s Global Center for Pathogen Research & Human Health, have performed the first comprehensive immunoprofiling study of patients with severe fever with thrombocytopenia syndrome (SFTS), an emerging tick-borne disease.

The World Health Organization has classified the virus that causes SFTS—called SFTSV—as among the most likely pathogens to cause widespread epidemics in the future. “The ticks that carry SFTSV have already been found in several states in the United States,” said Dr. Jung, “which signals the growing potential for a domestic outbreak and underscores the need to be doing research now that can help us to get out in front of this threat.”

According to the team’s findings published in mBio, B cells (the immune cells responsible for producing and secreting antibodies) play a crucial role in fatal SFTSV infections. This suggests that targeting B cells—particularly plasma B cells—may help prevent viral replication, although future studies will be necessary.

Variance in clinical manifestations and mortality

SFTS is characterized by many diverse symptoms—including high fever, gastrointestinal complications, low platelet and white blood cell counts, hemorrhage and multi-organ failure—and has a particularly high fatality rate. Interestingly, however, fatality rates vary dramatically by region, ranging anywhere from just over five percent to as high as 27 percent.

“Just for comparison,” Dr. Jung commented, “the mortality rates related to SFTSV infection are much higher than what we’re seeing with SARS-CoV-2 and COVID-19.”

Currently, the biological mechanisms behind these variances in disease symptoms and severity are unknown. In search of these answers, Kyle Jung, a graduate student in Dr. Jung’s lab, analyzed blood samples collected from more than 60 patients in South Korea between 2014 and 2019, including: 40 patients with active SFTSV infection; 11 patients who died from infection; 5 patients who recovered from infection; and 6 healthy controls.

Taking clues from patient serum

The researchers used precision technologies to uncover the protein and gene expression patterns of individual cells, comparing them across patients in different states of infection.

They found more than 70 inflammatory molecules in patient serum (the non-clotting component of blood) and identified associations between the presence and abundance of certain cytokines (immune stimulating proteins) and disease severity. Specifically, patient serum samples showed elevated levels of interferon gamma, interleukin 6, caspase 8, SIRT2, CCL7 and CSCL9 in high-risk patients compared to low-risk patients, and increased CCL20, TNFalpha and CX3CL1 in fatal patients.

These findings point to the possible utility of inflammatory biomarkers to help identify which patients infected with the virus are at least and greatest risk for severe disease and death.

The power of B cells in driving infection

Dr. Jung’s team also found that most viral genetic material localized to plasma B cells. Because B cells secrete antibodies, they are one of the main cell types involved in the body’s adaptive immune response. Compared to uninfected plasma B cells, those infected with SFTSV showed signs of reduced interferon signaling, which is a critical precursor to antibody production and secretion.

“Based on our findings, we believe that plasma B cells are the primary host for SFTSV replication,” said Dr. Jung. “Since we found that SFTSV infection suppresses neutralizing antibody production, once viral genetic material makes it into these B cells, the virus is free to replicate, spread and can cause subsequent death.”

Earlier this year, Dr. Jung—who also chairs the Department of Cancer Biology and holds the Betsy B. deWindt Endowed Chair in Cancer Biology—received a $2.8 million grant from the National Institute of Allergy and Infectious Diseases to develop a vaccine against SFTSV. Findings from this study will certainly provide valuable insights for Dr. Jung to build upon in his vaccine study.

Angela Park, PhD, a former lab member of Dr. Jung’s lab at the University of Southern California (USC), and Kyle Jung are first authors on the study, which was supported in part by the National Institutes of Health and made possible by close collaboration with Young-Ki Choi, PhD, from Chungbuk University in South Korea. Dr. Jung joined Lerner Research Institute from USC in August 2020.



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