Monocyte Chemoattractant Protein (MCP)-1 in Rotavirus-Associated White Matter Injury in Newborns

Author:

Yeom Jung Sook12,Jo Jae-Young3,Park Ji Sook12,Kim Young-Soo4,Chung Ju-Young5,Han Tae-Hee6,Seo Ji-Hyun12,Park Eun Sil12,Lim Jae-Young12,Woo Hyang-Ok12,Youn Hee-Shang12,Park Chan-Hoo27

Affiliation:

1. Department of Pediatrics, Gyeongsang National University School of Medicine, Jinju, Republic of Korea

2. Gyeongsang Institute of Health Science, Gyeongsang National University School of Medicine, Jinju, Republic of Korea

3. Department of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea

4. Department of Neurology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea

5. Department of Pediatrics, Sanggyepaik Hospital, Inje University College of Medicine, Seoul, Republic of Korea

6. Department of Diagnostic Laboratory Medicine, Sanggyepaik Hospital, Inje University College of Medicine, Seoul, Republic of Korea

7. Department of Pediatrics, Changwon Gyeongsang National University Hospital, Changwon, Republic of Korea

Abstract

AbstractRecent reports have suggested an association between rotavirus infection and a distinctive pattern of white matter injury (WMI) in neonates with seizures; however, the connection between the two is not fully understood. To evaluate the underlying mechanism, we profiled and compared eight cytokines (IL [interleukin]-1β, IL-6, IL-8, IL-10, IFN-γ [interferon-γ ], MCP-1 [monocyte chemoattractant protein-1], MIP-1β [macrophage inflammatory protein-1β], and TNF-α [tumor necrosis factor-α]) in the cerebrospinal fluid (CSF) of 33 neonates with seizures who had no other well-known causes of seizures and 13 control patients (rotavirus-induced gastroenteritis but without seizures). Among the 33 neonates with seizures, 9 showed WMI and all were infected with rotavirus (R + W + ). Among the 24 patients without WMI, 11 were infected with rotavirus (R + W − ) and 13 were not (R − W − ).Only MCP-1 and MIP-1β were different between the groups. MCP-1 was increased in R+ W+ compared with R + W− (p < 0.01), R − W− (p < 0.01), and control (p = 0.03) patients. MIP-1β was decreased in R + W+ compared with R − W− (p < 0.01) and control (p < 0.01), but not R + W− (p = 0.23) patients. MCP-1 and MIP-1β are C-C chemokines that recruit immune cells to the site of inflammation. Our pilot study suggests MCP-1-mediated monocyte recruitment may be linked with this complication caused by rotavirus.

Funder

National Research Foundation of Korea

Publisher

Georg Thieme Verlag KG

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

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