TY - JOUR
T1 - Partial MHC class II constructs as novel immunomodulatory therapy for stroke
AU - Benedek, Gil
AU - Vandenbark, Arthur A.
AU - Alkayed, Nabil J.
AU - Offner, Halina
N1 - Funding Information:
This work was supported by the National Institutes of Health [grant numbers R01NS075887, R01NS076013 (to HO); R42NS065515 (to HO and NJA)] and the Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Biomedical Laboratory Research and Development [grant number BX000226 (AAV)]. The contents do not represent the views of the Department of Veterans Affairs or the United States Government.
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2017/7
Y1 - 2017/7
N2 - The worldwide prevalence of stroke continues to rise despite recent successes in treating acute ischemic stroke. With limited patient eligibility and associated risk of tPA and mechanical thrombectomy, new preventive and therapeutic modalities are needed to stave the rising wave of stroke. Inflammation plays a key role in brain damage after cerebral ischemia, and novel therapies that target pro-inflammatory cells have demonstrated promise for treatment for stroke. Partial MHC class II constructs have been shown to prevent and/or reverse clinical signs of various inflammatory diseases such as experimental autoimmune encephalomyelitis, collagen-induced arthritis and experimental autoimmune uveitis, by reducing the number and frequency of activated cells in the damaged CNS. Herein, we review the use of partial MHC class II constructs as a novel treatment for ischemic stroke. These constructs have been shown to reduce infarct volume and neurological deficit in various cerebral ischemia models in young adult and aging male and female mice. In addition, partial MHC class II constructs were shown to reverse stroke-associated splenic atrophy and promote a protective M2 macrophage/microglia phenotype in the CNS which contributes to tissue repair and recovery after stroke. By addressing remaining STAIR criteria, such as efficacy in large animal models of stroke, these constructs will be prime candidates for clinical trials of acute ischemic stroke.
AB - The worldwide prevalence of stroke continues to rise despite recent successes in treating acute ischemic stroke. With limited patient eligibility and associated risk of tPA and mechanical thrombectomy, new preventive and therapeutic modalities are needed to stave the rising wave of stroke. Inflammation plays a key role in brain damage after cerebral ischemia, and novel therapies that target pro-inflammatory cells have demonstrated promise for treatment for stroke. Partial MHC class II constructs have been shown to prevent and/or reverse clinical signs of various inflammatory diseases such as experimental autoimmune encephalomyelitis, collagen-induced arthritis and experimental autoimmune uveitis, by reducing the number and frequency of activated cells in the damaged CNS. Herein, we review the use of partial MHC class II constructs as a novel treatment for ischemic stroke. These constructs have been shown to reduce infarct volume and neurological deficit in various cerebral ischemia models in young adult and aging male and female mice. In addition, partial MHC class II constructs were shown to reverse stroke-associated splenic atrophy and promote a protective M2 macrophage/microglia phenotype in the CNS which contributes to tissue repair and recovery after stroke. By addressing remaining STAIR criteria, such as efficacy in large animal models of stroke, these constructs will be prime candidates for clinical trials of acute ischemic stroke.
KW - Immunotherapy
KW - Inflammation
KW - Partial MHC class II construct
KW - Recombinant T-cell receptor ligand
KW - Stroke
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U2 - 10.1016/j.neuint.2016.10.007
DO - 10.1016/j.neuint.2016.10.007
M3 - Review article
C2 - 27773790
AN - SCOPUS:85006052085
SN - 0197-0186
VL - 107
SP - 138
EP - 147
JO - Neurochemistry International
JF - Neurochemistry International
ER -