Marie-Helene H Errera

Dr. Marie-Helene H Errera


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2018 in Emerging Infectious Diseases
Verified
Journal Article
Open access
APAna Catarina Pratas
Ana Catarina Pratas
PGPablo Goldschmidt
Pablo Goldschmidt
DLDavid Lebeaux
David Lebeaux
CAClaire Aguilar
Claire Aguilar
NENatalia Ermak
Natalia Ermak
MEMarie-Helene H Errera
Marie-Helene H Errera
We describe the frequency, demographic and clinical features, and visual outcomes of ocular syphilis infections observed during 2012–2015 at a tertiary reference center in Paris, France. Twenty-one cases (29 eyes) were identified. The occurrence of ocular syphilis increased from 1 case in 2012 to 5 cases in 2013, 6 cases in 2014, and 9 cases in 2015 (2.22–25.21/1,000 individual patients/year for the period). Among case-patients, an annual 20%–33% were co-infected with HIV. Seventy-six percent of ocular syphilis infections occurred in men who have sex with men. Seventy-five percent of case-patients had a good final visual outcome (best-corrected visual acuity >0.3 logMAR score). Visual outcome was worse for HIV-positive patients than for HIV-negative patients (p = 0.0139). At follow-up, the best visual outcomes were observed in patients whose mean time from first ocular symptom to consultation was 15 days (SD +19 days).

1 January 2022 in Survey of Ophthalmology
Verified
Journal Article
Closed access
SASupriya Arora
Supriya Arora
TSThamolwan Surakiatchanukul
Thamolwan Surakiatchanukul
TATarun Arora
Tarun Arora
MEMarie-Helene H Errera
Marie-Helene H Errera
HAHitesh Agrawal
Hitesh Agrawal
Jay ChhablaniJay Chhablani
Jay Chhablani

21 January 2022 in PLOS ONE
Verified
Journal Article
Open access
PDF file
MEMarie-Helene H Errera
Marie-Helene H Errera
APAna Pratas
Ana Pratas
SFSylvain Fisson
Sylvain Fisson
TMThomas Manicom
Thomas Manicom
MBMarouane Boubaya
Marouane Boubaya
CBCoralie Bloch-Queyrat
Coralie Bloch-Queyrat
To investigate which cytokines, chemokines and growth factors are involved in the immunopathogenesis of idiopathic uveitis, and whether cytokine profiles are associated with. Serum and aqueous humor (AH) samples of 75 patients with idiopathic uveitis were analyzed by multiplex immunoassay. Infectious controls consisted of 16 patients with ocular toxoplasmosis all confirmed by intraocular fluid analyses. Noninfectious controls consisted of 7 patients with Behçet disease related uveitis and 15 patients with sarcoidosis related uveitis. The control group consisted of AH and serum samples from 47 noninflammatory control patients with age-related cataract. In each sample, 27 immune mediators ± IL-21 and IL-23 were measured. In idiopathic uveitis, 13 of the 29 mediators, including most proinflammatory and vascular mediators such as IL-6, IL-8, IL-12, G-CSF, GM-CSF, MCP-1, IP-10, TNF-α and VEGF, were significantly elevated in the aqueous humor when compared to all controls. Moreover, IL-17, IP-10, and IL-21, were significantly elevated in the serum when compared to all controls. We clustered 4 subgroups of idiopathic uveitis using a statistical analysis of hierarchical unsupervised classification, characterized by the order of magnitude of concentrations of intraocular cytokines. The pathogenesis of idiopathic uveitis is characterized by the presence of predominantly proinflammatory cytokines and chemokines and vascular endothelial growth factor with high expression levels as compared to other causes of uveitis. There are indications for obvious Th-1/ IL21-Th17 pathways but also IL9-Th9 and increased IFN-γ-inducing cytokine (IL12) and IFN-γ-inducible CXC chemokine (IP-10). The combined data suggest that immune mediator expression is different among idiopathic uveitis. This study suggests various clusters among the idiopathic uveitis group rather than one specific uveitis entity.

21 January 2024 in Ophthalmology Science
Verified
Journal Article
Open access
YRYuhua Rui
Yuhua Rui
MZMin Zhang
Min Zhang
DLDaniel M.W. Lee
Daniel M.W. Lee
VSValerie C. Snyder
Valerie C. Snyder
RRRashmi Raghuraman
Rashmi Raghuraman
EREthan A. Rossi
Ethan A. Rossi
Putative microglia were recently detected using adaptive optics ophthalmoscopy in healthy eyes. Here we evaluate the use of nonconfocal adaptive optics scanning light ophthalmoscopy (AOSLO) for quantifying the morphology and motility of presumed microglia and other immune cells in eyes with retinal inflammation from uveitis and healthy eyes. Observational exploratory study. Twelve participants were imaged, including 8 healthy participants and 4 posterior uveitis patients recruited from the clinic of 1 of the authors (M.H.E.). The Pittsburgh AOSLO imaging system was used with a custom-designed 7-fiber optical fiber bundle for simultaneous confocal and nonconfocal multioffset detection. The inner retina was imaged at several locations at multiple timepoints in healthy participants and uveitis patients to generate time-lapse images. Microglia and macrophages were manually segmented from nonconfocal AOSLO images, and their morphological characteristics quantified (including soma size, diameter, and circularity). Cell soma motion was quantified across time for periods of up to 30 minutes and their speeds were calculated by measuring their displacement over time. A spectrum of cell morphologies was detected in healthy eyes from circular amoeboid cells to elongated cells with visible processes, resembling activated and ramified microglia, respectively. Average soma diameter was 16.1 ± 0.9 μm. Cell movement was slow in healthy eyes (0.02 μm/sec on average), but macrophage-like cells moved rapidly in some uveitis patients (up to 3 μm/sec). In an eye with infectious uveitis, many macrophage-like cells were detected; during treatment their quantity and motility decreased as vision improved. In vivo adaptive optics ophthalmoscopy offers promise as a potentially powerful tool for detecting and monitoring inflammation and response to treatment at a cellular level in the living eye. Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

17 February 2021 in Ocular Immunology and Inflammation
Verified
Journal Article
Open access
CMCéline Mebsout-Pallado
Céline Mebsout-Pallado
RORaphaëlle Orès
Raphaëlle Orès
CTCéline Terrada
Céline Terrada
KDKunal K. Dansingani
Kunal K. Dansingani
Jay ChhablaniJay Chhablani
Jay Chhablani
MEMarie-Helene H Errera
Marie-Helene H Errera
To describe the application of OCT-A in various posterior uveitis disorders in our experience and to compare it with the available literature. Eighteen eyes with the diagnoses of multifocal choroid...

24 March 2020 in Nutrients
Verified
Journal Article
Open access
PDF file
IMIngrid Munia
Ingrid Munia
LGLaurent Gafray
Laurent Gafray
MBMarie-Agnès Bringer
Marie-Agnès Bringer
PGPablo Goldschmidt
Pablo Goldschmidt
LPLil Proukhnitzky
Lil Proukhnitzky
IRIsabelle Ranchon-Cole
Isabelle Ranchon-Cole
Retinal pigment epithelial cells are crucial for retina maintenance, making their cytoprotection an excellent way to prevent or slow down retinal degeneration. In addition, oxidative stress, inflammation, apoptosis, neovascularization, and/or autophagy are key pathways involved in degenerative mechanisms. Therefore, here we studied the effects of curcumin, lutein, and/or resveratrol on human retinal pigment epithelial cells (ARPE-19). Cells were incubated with individual or combined agent(s) before induction of (a) H2O2-induced oxidative stress, (b) staurosporin-induced apoptosis, (c) CoCl2-induced hypoxia, or (d) a LED-autophagy perturbator. Metabolic activity, cellular survival, caspase 3/7 activity (casp3/7), cell morphology, VEGF levels, and autophagy process were assessed. H2O2 provoked a reduction in cell survival, whereas curcumin reduced metabolic activity which was not associated with cell death. Cell death induced by H2O2 was significantly reduced after pre-treatment with curcumin and lutein, but not resveratrol. Staurosporin increased caspase-3/7 activity (689%) and decreased cell survival by 32%. Curcumin or lutein protected cells from death induced by staurosporin. Curcumin, lutein, and resveratrol were ineffective on the increase of caspase 3/7 induced by staurosporin. Pre-treatment with curcumin or lutein prevented LED-induced blockage of autophagy flux. Basal-VEGF release was significantly reduced by lutein. Therefore, lutein and curcumin showed beneficial protective effects on human-derived retinal cells against several insults.