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Daniel J. Stieh

Researcher at Janssen Pharmaceutica

Publications -  30
Citations -  1182

Daniel J. Stieh is an academic researcher from Janssen Pharmaceutica. The author has contributed to research in topics: Vaccination & Medicine. The author has an hindex of 14, co-authored 24 publications receiving 917 citations. Previous affiliations of Daniel J. Stieh include St George's Hospital & Northwestern University.

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Journal ArticleDOI

Evaluation of a mosaic HIV-1 vaccine in a multicentre, randomised, double-blind, placebo-controlled, phase 1/2a clinical trial (APPROACH) and in rhesus monkeys (NHP 13-19)

Dan H. Barouch, +58 more
- 21 Jul 2018 - 
TL;DR: All vaccine regimens demonstrated favourable safety and tolerability and immunogenicity and protective efficacy against a series of six repetitive, heterologous, intrarectal challenges with a rhesus peripheral blood mononuclear cell-derived challenge stock of simian-human immunodeficiency virus (SHIV-SF162P3).
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Th17 Cells Are Preferentially Infected Very Early after Vaginal Transmission of SIV in Macaques.

TL;DR: This analysis identifies Th17-lineage CCR6+ CD4+ T cells as primary targets of SIV during vaginal transmission, which opens new opportunities for interventions to protect these cells and prevent HIV transmission.
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Human cervicovaginal mucus contains an activity that hinders HIV-1 movement.

TL;DR: A previously unknown activity in CVM is revealed that is capable of impeding HIV-1 mobility to enhance mucosal barrier function and was significantly hindered in the same CVM samples in which bead diffusion was unhindered.
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Cyanovirin-N potently inhibits human immunodeficiency virus type 1 infection in cellular and cervical explant models

TL;DR: Data presented here indicate that targeting HIV envelope glycoproteins may provide an effective strategy to prevent HIV-1 infection mediated by either cell-free virus or infected cells.
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Vaginal challenge with an SIV-based dual reporter system reveals that infection can occur throughout the upper and lower female reproductive tract.

TL;DR: It is essential that protective mechanisms for prevention of HIV acquisition must be present at protective levels throughout the entire FRT to provide complete protection.