2023
DOI: 10.3390/cancers15113046
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Follicular Helper and Regulatory T Cells Drive the Development of Spontaneous Epstein–Barr Virus Lymphoproliferative Disorder

Elshafa Hassan Ahmed,
Mark Lustberg,
Claire Hale
et al.

Abstract: Epstein–Barr virus (EBV) is a ubiquitous herpes virus associated with various cancers. EBV establishes latency with life-long persistence in memory B-cells and can reactivate lytic infection placing immunocompromised individuals at risk for EBV-driven lymphoproliferative disorders (EBV-LPD). Despite the ubiquity of EBV, only a small percentage of immunocompromised patients (~20%) develop EBV-LPD. Engraftment of immunodeficient mice with peripheral blood mononuclear cells (PBMCs) from healthy EBV-seropositive d… Show more

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Cited by 2 publications
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“…Each sample and the corresponding standard EBV was detected using the EBNA1 gene and performed with 10 ng of sample DNA as the initial concentration using the ViiA7 Real-time qPCR machine (Applied Biosystems, Waltham, MA USA). EBV DNA was quantified with primers specific to the EBV EBNA1 locus (forward: TCATCATCATCCGGGTCTCC, reverse: CCTACAGGGTGGAAAAATGGC), and signals were normalized to host genome DNA using primers specific for human ACTB (forward: CAGGCAGCTCGTAGCTCTTC, reverse: TCGTGCGTGACATTAAGGAG) [22]. With a total reaction volume of 10 µL, the reaction was carried out using 5 µL of 2× Fast SYBR Green Master Mix (Applied Biosystems, Waltham, MA USA), 0.25 µL of forward (10 µM) and 0.25 µL of reverse (10 µM) primers, 2.5 µL of PCR-grade water, and 2 µL of 5 ng/µL DNA concentration.…”
Section: Real-time Quantification Pcr From Genomic Dna For Ebv Load/c...mentioning
confidence: 99%
“…Each sample and the corresponding standard EBV was detected using the EBNA1 gene and performed with 10 ng of sample DNA as the initial concentration using the ViiA7 Real-time qPCR machine (Applied Biosystems, Waltham, MA USA). EBV DNA was quantified with primers specific to the EBV EBNA1 locus (forward: TCATCATCATCCGGGTCTCC, reverse: CCTACAGGGTGGAAAAATGGC), and signals were normalized to host genome DNA using primers specific for human ACTB (forward: CAGGCAGCTCGTAGCTCTTC, reverse: TCGTGCGTGACATTAAGGAG) [22]. With a total reaction volume of 10 µL, the reaction was carried out using 5 µL of 2× Fast SYBR Green Master Mix (Applied Biosystems, Waltham, MA USA), 0.25 µL of forward (10 µM) and 0.25 µL of reverse (10 µM) primers, 2.5 µL of PCR-grade water, and 2 µL of 5 ng/µL DNA concentration.…”
Section: Real-time Quantification Pcr From Genomic Dna For Ebv Load/c...mentioning
confidence: 99%