109 Zina Pitcher Pl, 5019 AAT-BSRB
Ann Arbor, MI 48109
Available to mentor
Dr. Murdock is the Robert A. Epstein and Joan M. Chernoff-Epstein Emerging Scholar. He is interested in the immune system’s responses in ALS. His work cuts across a broad spectrum of analyses from translational work using clinical samples to mouse models of disease to in vitro analyses of immune function in ALS. His work focuses particularly on three types of immune cells – neutrophils, natural killer (NK) cells, and CD4 T cells - and their roles in controlling ALS progression. Neutrophils are the most common immune cell in the blood and have been implicated in a number of neurodegenerative diseases, including ALS. These cells are some of the first responders to neuronal damage but can often make disease worse, rather than aiding the repair response. In ALS, Dr. Murdock has shown that increased neutrophil levels are associated with more rapid disease progression, and neutrophil levels are the single best indicator of future disease progression based on predictive models. Similarly, NK cells protect the body from infection and cancer, but also kill dying cells. Research has also found that the molecule that protects the body from its own NK cells is missing on the surface of motor neurons during ALS suggesting that NK cells may target motor neurons during disease. Dr. Murdock’s studies have also linked NK cells to ALS progression, and ongoing studies are using immune-modifying drugs to target NK cells in ALS to try and extend patient survival. Conversely, CD4 T cells, the master control cells of the immune system, disappear from the blood during ALS, and studies in mice and humans demonstrate that loss of CD4 T cells is associated with disease acceleration. Dr. Murdock’s team is currently trying to identify which group of CD4 T cells or which immune mechanism slows ALS progression. These observations have led to preclinical ALS studies utilizing a currently FDA-approved drug, and if successful, this drug will be tested in clinical trials in ALS patients. Dr. Murdock has obtained a patent on the use of this drug in ALS patients if these trials are successful.
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Postdoctoral Research FellowUniversity of Michigan, Neurology, 2015
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Post Doctoral Research FellowUniversity of Michigan/Ann Arbor Veterans Affairs Healthcare System, Division of Pulmonary and Critical Care Medicine, 2014
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Postdoctoral FellowUniversity of Michigan, Microbiology and Immunology, 2014
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PhD, ImmunologyUniversity of Michigan, Ann Arbor, 2010
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BS, Microbiology, Immunology, and Molecular GeneticsUniversity of California, Los Angeles, 2003
- Immunology in ALS
- Immunology in diabetic neuropathy
- Immunology in brain health
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Elzinga SE, Henn R, Murdock BJ, Kim B, Hayes JM, Mendelson F, Webber-Davis I, Teener S, Pacut C, Lentz SI, Feldman EL. Front Immunol, 2022 13: 1012594Journal ArticlecGAS/STING and innate brain inflammation following acute high-fat feeding.
DOI:10.3389/fimmu.2022.1012594 PMID: 36248795 -
Murdock B. 2022 Aug 25;PresentationImmune Changes Precede Clinical Changes in ALS
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Murdock B. 2022 Aug 25;PresentationImmune Changes Precede Clinical Changes in ALS
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Murdock B. 2022 May 4;PresentationTofacitinib as a Novel Therapeutic in C9 ALS mice
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Murdock B. 2022 May 4;PresentationTofacitinib as a Novel Therapeutic in C9 ALS mice
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2021 Dec 1;PresentationImmunity in ALS
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2021 Oct 1;PresentationPatient Demographics and Disease Mechanisms:Sex and Age Alter Immunity in ALS
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2021 Oct 1;PresentationSex and age impact the role of the immune system in amyotrophic lateral sclerosis