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. 2016 Sep 7;37(10):715. doi: 10.1016/j.it.2016.08.003

Harnessing Nanoparticles for Immune Modulation

(Trends in Immunology 36, 419–427; July 2016)

Daniel R Getts , Lonnie D Shea, Stephen D Miller, Nicholas JC King
PMCID: PMC8445247  PMID: 27614797

Due to an oversight in the preparation of this Review article, the authors inadvertently included a “rat” model for “Complete LAD occlusion” in Table 1 . Findings on “Japanese encephalitis” were erroneously attributed to reference 8 but are unpublished observations. Table 1 was modified to reflect those changes and the corrected version is included below. That authors apologize for these errors and assert that they make no difference to the line of discussion of this review.

Table 1.

IMP Efficacy in Severe Inflammation Models.

Condition Animal model Species Outcome Refs
Acute myocardial infarction Temporary LAD occlusion
Complete LAD occlusion
Mouse
Mouse
Reduced inflammation, reduced infarct size
Increased function
[8]
Kidney ischemia Temporary renal artery occlusion Mouse Reduced tubular necrosis and increased function [8]
Stroke Temporary carotid artery Mouse Reduced inflammation Unpublished
MS relapse EAE SJL (relapsing–remitting)
EAE C57BL/6 (progressive disease)
Mouse
Mouse
Reduced symptoms, reduced inflammation and demyelination [8]
IBD DSS colitis Mouse Reduced symptoms, reduced inflammation, rapid recovery of the colon [8]
Acute encephalitis syndrome WNV encephalitis
Japanese encephalitis
Mouse
Mouse
Increased survival
Increased survival
[8]
Unpublished
Spinal cord injury Spinal cord crush Mouse Increased mobility, reduced inflammation Unpublished

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