Vaccine formulations in clinical development for the prevention of severe acute respiratory syndrome coronavirus 2 infection

CJ Batty, MT Heise, EM Bachelder… - Advanced drug delivery …, 2021 - Elsevier
The COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2
(SARS-CoV-2) has led to an unprecedented effort toward the development of an effective …

[HTML][HTML] Fighting COVID-19: A quick review of diagnoses, therapies, and vaccines

HI Shih, CJ Wu, YF Tu, CY Chi - Biomedical journal, 2020 - Elsevier
Abstract The coronavirus disease 2019 (COVID-19) pandemic caused by a novel
coronavirus, SARS-CoV-2, has infected more than 22 million individuals and resulted in …

The inside out of lentiviral vectors

S Durand, A Cimarelli - Viruses, 2011 - pmc.ncbi.nlm.nih.gov
Lentiviruses induce a wide variety of pathologies in different animal species. A common
feature of the replicative cycle of these viruses is their ability to target non-dividing cells, a …

Combinatorial approaches to effective therapy in glioblastoma (GBM): Current status and what the future holds

S Asija, A Chatterjee, S Yadav, G Chekuri… - International Reviews …, 2022 - Taylor & Francis
The aggressive and recurrent nature of glioblastoma is multifactorial and has been attributed
to its biological heterogeneity, dysfunctional metabolic signaling pathways, rigid blood–brain …

A simple, versatile and efficient method to genetically modify human monocyte-derived dendritic cells with HIV-1–derived lentiviral vectors

G Berger, S Durand, C Goujon, XN Nguyen… - Nature protocols, 2011 - nature.com
Lentiviral vectors derived from the human immunodeficiency type 1 virus (HIV-1 LV) are
among the finest tools available today for the genetic modification of human monocyte …

Transduction of modified factor VIII gene improves lentiviral gene therapy efficacy for hemophilia A

J Gong, TH Chung, J Zheng, H Zheng… - Journal of Biological …, 2021 - ASBMB
Hemophilia A (HA) is a bleeding disorder caused by deficiency of the coagulation factor VIII
(F8). F8 replacement is standard of care, whereas gene therapy (F8 gene) for HA is an …

Small interfering RNA (siRNA) delivery into monocyte-derived dendritic cells by electroporation

AT Prechtel, NM Turza, AA Theodoridis… - Journal of …, 2006 - Elsevier
Selective gene silencing by small interfering RNAs (siRNAs) has been shown to be an
efficient method for the targeted manipulation of cellular functions. Chemical transfection …

HIV-1-derived lentiviral vectors directly activate plasmacytoid dendritic cells, which in turn induce the maturation of myeloid dendritic cells

M Rossetti, S Gregori, E Hauben, BD Brown… - Human gene …, 2011 - liebertpub.com
Lentiviral vectors (LV) can induce type I interferon (IFN I) production from murine
plasmacytoid dendritic cells (pDC), but not myeloid (my) DC. Here, we investigated whether …

From pathogen to medicine: HIV‐1‐derived lentiviral vectors as vehicles for dendritic cell based cancer immunotherapy

M Dullaers, K Thielemans - The Journal of Gene Medicine: A …, 2006 - Wiley Online Library
Over the years, the unique capacity of dendritic cells (DC) for efficient activation of naive T
cells has led to their extensive use in cancer immunotherapy protocols. In order to be able to …

An effective cancer vaccine modality: lentiviral modification of dendritic cells expressing multiple cancer-specific antigens

B Wang, J He, C Liu, LJ Chang - Vaccine, 2006 - Elsevier
Viral modification of dendritic cells (DCs) may deliver a “danger signal” critical to the hypo-
reactive DCs in cancer patients. Using three highly differentially expressed hepatoma tumor …