Frédéric Pène

Prof. Dr. Frédéric Pène


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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7 August 2020 in Science
Verified
Journal Article
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JHJérôme Hadjadj
Jérôme Hadjadj
NYNader Yatim
Nader Yatim
LBLaura Barnabei
Laura Barnabei
ACAurélien Corneau
Aurélien Corneau
JBJeremy Boussier
Jeremy Boussier
BTBenjamin Terrier
Benjamin Terrier
Interferons interfere with lung repair: Interferons (IFNs) are central to antiviral immunity. Viral recognition elicits IFN production, which in turn triggers the transcription of IFN-stimulated genes (ISGs), which engage in various antiviral functions. Type I IFNs (IFN-α and IFN-β) are widely expressed and can result in immunopathology during viral infections. By contrast, type III IFN (IFN-λ) responses are primarily restricted to mucosal surfaces and are thought to confer antiviral protection without driving damaging proinflammatory responses. Accordingly, IFN-λ has been proposed as a therapeutic in coronavirus disease 2019 (COVID-19) and other such viral respiratory diseases (see the Perspective by Grajales-Reyes and Colonna). Broggi et al. report that COVID-19 patient morbidity correlates with the high expression of type I and III IFNs in the lung. Furthermore, IFN-λ secreted by dendritic cells in the lungs of mice exposed to synthetic viral RNA causes damage to the lung epithelium, which increases susceptibility to lethal bacterial superinfections. Similarly, using a mouse model of influenza infection, Major et al. found that IFN signaling (especially IFN-λ) hampers lung repair by inducing p53 and inhibiting epithelial proliferation and differentiation. Complicating this picture, Hadjadj et al. observed that peripheral blood immune cells from severe and critical COVID-19 patients have diminished type I IFN and enhanced proinflammatory interleukin-6– and tumor necrosis factor-α–fueled responses. This suggests that in contrast to local production, systemic production of IFNs may be beneficial. The results of this trio of studies suggest that the location, timing, and duration of IFN exposure are critical parameters underlying the success or failure of therapeutics for viral respiratory infections. Science , this issue p. 706 , p. 712 , p. 718 ; see also p. 626

1 August 2013 in Journal of Clinical Oncology
Verified
Journal Article
Closed access
EAElie Azoulay
Elie Azoulay
DMDjamel Mokart
Djamel Mokart
FPFrédéric Pène
Frédéric Pène
JLJérôme Lambert
Jérôme Lambert
AKAchille Kouatchet
Achille Kouatchet
VLVirginie Lemiale
Virginie Lemiale
Purpose: Patients with hematologic malignancies are increasingly admitted to the intensive care unit (ICU) when life-threatening events occur. We sought to report outcomes and prognostic factors in these patients. Patients and Methods: Ours was a prospective, multicenter cohort study of critically ill patients with hematologic malignancies. Health-related quality of life (HRQOL) and disease status were collected after 3 to 6 months. Results: Of the 1,011 patients, 38.2% had newly diagnosed malignancies, 23.1% were in remission, and 24.9% had received hematopoietic stem-cell transplantations (HSCT, including 145 allogeneic). ICU admission was mostly required for acute respiratory failure (62.5%) and/or shock (42.3%). On day1, 733 patients (72.5%) received life-supporting interventions. Hospital, day-90, and 1-year survival rates were 60.7%, 52.5%, and 43.3%, respectively. By multivariate analysis, cancer remission and time to ICU admission less than 24 hours were associated with better hospital survival. Poor performance status, Charlson comorbidity index, allogeneic HSCT, organ dysfunction score, cardiac arrest, acute respiratory failure, malignant organ infiltration, and invasive aspergillosis were associated with higher hospital mortality. Mechanical ventilation (47.9% of patients), vasoactive drugs (51.2%), and dialysis (25.9%) were associated with mortality rates of 60.5%, 57.5%, and 59.2%, respectively. On day 90, 80% of survivors had no HRQOL alterations (physical and mental health similar to that of the overall cancer population). After 6 months, 80% of survivors had no change in treatment intensity compared with similar patients not admitted to the ICU, and 80% were in remission. Conclusion: Critically ill patients with hematologic malignancies have good survival, disease control, and post-ICU HRQOL. Earlier ICU admission is associated with better survival.

27 October 2015 in JAMA
Verified
Journal Article
Open access
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VLVirginie Lemiale
Virginie Lemiale
DMDjamel Mokart
Djamel Mokart
MRMatthieu Resche-Rigon
Matthieu Resche-Rigon
FPFrédéric Pène
Frédéric Pène
JMJulien Mayaux
Julien Mayaux
F(For The Groupe de Recherche En Réanimation Respiratoire du Patient D’onco-Hématologie (Grrr-Oh)
For The Groupe de Recherche En Réanimation Respiratoire du Patient D’onco-Hématologie (Grrr-Oh)
Quiz Ref ID The number of patients living with immune deficiencies is increasing steadily.1,2 These patients are at high risk for life-threatening complications, especially acute respiratory failure warranting admission to the intensive care unit (ICU).3 Mortality in this situation has ranged from 40% to 90% and remains high, despite improvements in recent years.4,5 Invasive mechanical ventilation strongly predicts mortality,6 possibly because of the risks of ventilation itself, which has prompted efforts to determine whether acute respiratory failure can be safely managed without intubation.

1 October 2003 in Clinical Infectious Diseases
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Journal Article
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FPFrédéric Pène
Frédéric Pène
AMAnnabelle Merlat
Annabelle Merlat
AVAstrid Vabret
Astrid Vabret
FRFlore Rozenberg
Flore Rozenberg
ABAgnès Buzyn
Agnès Buzyn
PLPierre Lebon
Pierre Lebon
Coronaviruses strains 229E and OC43 have been associated with various respiratory illnesses ranging from the self-resolving common cold to severe pne

1 March 2011 in Circulation
Verified
Journal Article
Closed access
PDF file
FDFlorence Dumas
Florence Dumas
DGDavid Grimaldi
David Grimaldi
BZBenjamin Zuber
Benjamin Zuber
JFJérôme Fichet
Jérôme Fichet
JCJulien Charpentier
Julien Charpentier
ACAlain Cariou
Alain Cariou
Background—: Although the level of evidence of improvement is significant in cardiac arrest patients resuscitated from a shockable rhythm (ventricular fibrillation or pulseless ventricular tachycardia [VF/V t ]), the use of therapeutic mild hypothermia (TMH) is more controversial in nonshockable patients (pulseless electric activity or asystole [PEA/asystole]). We therefore assessed the prognostic value of hypothermia for neurological outcome at hospital discharge according to first-recorded cardiac rhythm in a large cohort. Methods and Results—: Between January 2000 and December 2009, data from 1145 consecutive out-of-hospital cardiac arrest patients in whom a successful resuscitation had been achieved were prospectively collected. The association of TMH with a good neurological outcome at hospital discharge (cerebral performance categories level 1 or 2) was quantified by logistic regression analysis. TMH was induced in 457/708 patients (65%) in VF/V t and in 261/437 patients (60%) in PEA/asystole. Overall, 342/1145 patients (30%) reached a favorable outcome (cerebral performance categories level 1 or 2) at hospital discharge, respectively 274/708 (39%) in VF/V t and 68/437 (16%) in PEA/asystole ( P <0.001). After adjustment, in VF/V t patients, TMH was associated with increased odds of good neurological outcome (adjusted odds ratio, 1.90; 95% confidence interval, 1.18 to 3.06) whereas in PEA/asystole patients, TMH was not significantly associated with good neurological outcome (adjusted odds ratio, 0.71; 95% confidence interval, 0.37 to 1.36). Conclusions—: In this large cohort of cardiac arrest patients, hypothermia was independently associated with an improved outcome at hospital discharge in patients presenting with VF/V t . By contrast, TMH was not associated with good outcome in nonshockable patients. Further investigations are needed to clarify this lack of efficiency in PEA/asystole.

23 September 2002 in Oncogene
Verified
Journal Article
Closed access
FPFrédéric Pène
Frédéric Pène
YCYann-Erick Claessens
Yann-Erick Claessens
OMOdile Muller
Odile Muller
FVFranck Viguié
Franck Viguié
PMPatrick Mayeux
Patrick Mayeux
DBDidier Bouscary
Didier Bouscary