Key result
Antibodies clear CNS viral encephalomyelitis via canonical and non-canonical noncytolytic functions.
Why the study?
Acute RNA viral encephalomyelitis is a serious complication of numerous virus infections, and understanding the immune-specialized zone of the CNS is essential for developing effective treatments.
Understanding the noncytolytic functions of antibodies in the immune-specialized CNS may guide novel therapeutics for treating viral encephalomyelitis without destroying irreplaceable neurons.
May guide neuron-sparing antibody therapies for viral encephalomyelitis; leaves open need for clinical validation studies.
Acute RNA viral encephalomyelitis is a serious complication of numerous virus infections. Antibodies in the cerebral spinal fluid (CSF) are correlated to better outcomes, and there is substantive evidence of antibody secreting cells (ASCs) entering the central nervous system (CNS) and contributing to resolution of infection. Here, we review the RNA viruses known to cause acute viral encephalomyelitis with mechanisms of control that require antibody or ASCs. We compile the cytokines, chemokines, and surface receptors associated with ASC recruitment to the CNS after infection and compare known antibody-mediated mechanisms as well as potential noncytolytic mechanisms for virus control. These non-canonical functions of antibodies may be employed in the CNS to protect precious non-renewable neurons. Understanding the immune-specialized zone of the CNS is essential for the development of effective treatments for acute encephalomyelitis caused by RNA viruses.
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Bartlett et al. (2020) conducted a review in Acute RNA viral encephalomyelitis. Antibodies and antibody-secreting cells in the CNS was evaluated. Antibodies and antibody-secreting cells possess canonical and non-canonical noncytolytic functions that contribute to the clearance of acute RNA viral encephalomyelitis from the CNS.
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