Natural Killer cell transcriptome during primary EBV infection and EBV associated Hodgkin Lymphoma in children-A preliminary observation.


Journal

Immunobiology
ISSN: 1878-3279
Titre abrégé: Immunobiology
Pays: Netherlands
ID NLM: 8002742

Informations de publication

Date de publication:
05 2020
Historique:
received: 13 12 2019
revised: 09 01 2020
accepted: 25 01 2020
pubmed: 12 2 2020
medline: 7 8 2021
entrez: 12 2 2020
Statut: ppublish

Résumé

Epstein Barr Viral infection is a common childhood infection in India and is also nearly 100 % etiologically associated with pediatric Hodgkin Lymphoma (HL). The main question in EBV immunobiology has been, why only a small subset of infected individuals develop EBV associated malignancies, while the vast majority carry this virus asymptomatically for life. Natural Killer (NK) cells, with a phenotype of CD56dim CD16+ exhibit potent cytotoxicity towards both virus infected cells and transformed cells and hence have been considered to be crucial in preventing the development of symptomatic EBV infection and lymphoma. In order to get an insight into the various possible molecular aspects of NK cells, in the pathogenesis of both these EBV mediated diseases in children we studied the whole transcriptome of MACS sorted CD56dim CD16 + NK cells from four patients from each of the three groups of children viz. Infectious Mononucleosis (IM), HL and age matched controls by using a massively parallel sequencing approach. NK cells from both IM and HL had down-regulated innate immunity and chemokine signaling genes. While down-regulation of genes responsible for polarization of the secretory apparatus, activated NK cell signaling and MAP kinase signaling were exclusive to NK cells in patients with IM, in NK cells of HL, specifically, genes involved in extracellular matrix (ECM) - receptor interaction, cytokine-cytokine receptor interaction, TNF signaling, Toll-like receptor signaling pathway and cytosolic DNA-sensing pathways were significantly down-regulated. Enrichment analysis showed STAT3 to be the most significant transcription factor (TF) for the down-regulated genes in IM, whereas, GATA1 was found to be the most significant TF for the genes down-regulated in HL. Analysis of protein interaction network identified functionally important protein clusters. Top clusters, comprised of down-regulated genes, involved in signaling and ubiquitin-related processes and pathways. These may perhaps be responsible for the hypo-responsiveness of NK cells in both diseases. These possibly point to different deficiencies in NK cell activation, loss of activating receptor signaling and degranulation in IM, versus loss of cytokine and chemokine signaling in HL, in the two EBV associated pathologies investigated. Various suppressed molecules and pathways were novel, which have not been reported earlier and could therefore be potential targets for immunotherapy of NK cell reactivation in both the diseases in future.

Identifiants

pubmed: 32044149
pii: S0171-2985(19)30417-6
doi: 10.1016/j.imbio.2020.151907
pii:
doi:

Substances chimiques

Biomarkers 0
Cytokines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

151907

Informations de copyright

Copyright © 2020 Elsevier GmbH. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest AKK was also the founder director of a private limited company, Shodhaka Life Sciences Pvt. Ltd., during the research period, and DS was an employee of that company. Anup Chugani, Vishnu Priya R are employees of a private company Medgenome. Declaration of interest for other authors – none.

Auteurs

Alka M (A)

Departments of Microbiology, Kidwai Memorial Institute of Oncology, Bangalore, India.

Shatakshee Chatterjee (S)

National Institute of Biomedical Genomics, Kalyani, West Bengal, India.

Parchure A (P)

Departments of Microbiology, Kidwai Memorial Institute of Oncology, Bangalore, India.

Mahantesh S (M)

Departments of Microbiology, Indira Gandhi Institute of Child Health, Bangalore, India.

Sravanthi Davuluri (S)

Biological Data Analyzers' Association (BdataA), Electronic City, Phase I, Bangalore, India.

Arun Kumar Ar (AK)

Departments of Pediatric Oncology, Kidwai Memorial Institute of Oncology, India.

Avinash T (A)

Departments of Pediatric Oncology, Kidwai Memorial Institute of Oncology, India.

Padma M (P)

Departments of Pediatric Oncology, Kidwai Memorial Institute of Oncology, India.

Premalata Cs (P)

Departments of Pathology, Kidwai Memorial Institute of Oncology, Bangalore, India.

Mahua Sinha (M)

Departments of Microbiology, Kidwai Memorial Institute of Oncology, Bangalore, India.

Anup Chugani (A)

MedGenome Labs Ltd., Bangalore, India.

Vishnu Priya R (VP)

MedGenome Labs Ltd., Bangalore, India.

Acharya Kk (A)

Biological Data Analyzers' Association (BdataA), Electronic City, Phase I, Bangalore, India; Institute of Bioinformatics and Applied Biotechnology, Bangalore, India.

Jayshree R S (J)

Departments of Microbiology, Kidwai Memorial Institute of Oncology, Bangalore, India. Electronic address: microjayshree@gmail.com.

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Classifications MeSH