Imaging immunological processes from blood to brain in amyotrophic lateral sclerosis.
Sandra AmorErik NutmaManuel MarzinFabiola PuentesPublished in: Clinical and experimental immunology (2021)
Neuropathology studies of amyotrophic lateral sclerosis (ALS) and animal models of ALS reveal a strong association between aberrant protein accumulation and motor neurone damage, as well as activated microglia and astrocytes. While the role of neuroinflammation in the pathology of ALS is unclear, imaging studies of the central nervous system (CNS) support the idea that innate immune activation occurs early in disease in both humans and rodent models of ALS. In addition, emerging studies also reveal changes in monocytes, macrophages and lymphocytes in peripheral blood as well as at the neuromuscular junction. To more clearly understand the association of neuroinflammation (innate and adaptive) with disease progression, the use of biomarkers and imaging modalities allow monitoring of immune parameters in the disease process. Such approaches are important for patient stratification, selection and inclusion in clinical trials, as well as to provide readouts of response to therapy. Here, we discuss the different imaging modalities, e.g. magnetic resonance imaging, magnetic resonance spectroscopy and positron emission tomography as well as other approaches, including biomarkers of inflammation in ALS, that aid the understanding of the underlying immune mechanisms associated with motor neurone degeneration in ALS.
Keyphrases
- amyotrophic lateral sclerosis
- peripheral blood
- high resolution
- magnetic resonance imaging
- positron emission tomography
- computed tomography
- clinical trial
- oxidative stress
- innate immune
- traumatic brain injury
- immune response
- genome wide
- randomized controlled trial
- lipopolysaccharide induced
- gene expression
- neuropathic pain
- cognitive impairment
- multiple sclerosis
- inflammatory response
- spinal cord injury
- cerebral ischemia
- dendritic cells
- case control
- fluorescence imaging
- bone marrow
- protein protein
- replacement therapy