24 research outputs found
Je suis enrhumeÌ du cerveau : sceÌne comique
Je suis enrhumĂ© du cerveau!J\u27ai la tĂȘteen capilotade,Je sens mon esprit qui s\u27Ă©vade,Plaignez-moi, je suis tout en eau! atchum atchum,Je suis enrhumĂ© du cerveau!
Sans mentir, bien sur, j\u27Ă©ternueChaque jour au moins deux cents fois.Un vrouillard obscurcit ma vue,Je ne sais plus ce que je vois.Cela m\u27abime le physique,J\u27ai le nez bleu, blanc, rouge et noir;Et je fais avec mon mouchoir,Une bien drĂŽle de musique
Prominent Plasmacytosis Following Intravenous Immunoglobulin Correlates with Clinical Improvement in Guillain-Barré Syndrome
BACKGROUND: High doses of pooled polyclonal IgG are commonly used to treat numerous autoimmune diseases. Their mode of action nevertheless remains only partially explained. At the same time, until now, no early biological marker has been able to predict their efficacy. METHODOLOGY/PRINCIPAL FINDINGS: In a first pilot retrospective analysis, we reviewed white blood cell counts and blood smears in consecutive patients with autoimmune disease (n = 202) and non-autoimmune disease (n = 104). Autoimmune patients received either intravenous immunoglobulin (IVIg, n = 103), plasma exchange (n = 78) or no specific treatment (n = 21). We then prospectively monitored consecutive autoimmune patients with IVIg injection (n = 67), or without any specific treatment (n = 10) using the same routine laboratory tests, as well as flow cytometry. Both retrospective and prospective analyses identified large plasma-cell mobilization exclusively in IVIg-treated autoimmune patients 7 days after initiation of treatment. The majority of IVIg-mobilized plasma cells were immature HLA-DR(high)/CD138(low)/CXCR4(low) plasma cells expressing intracellular immunoglobulin G which were neither IVIg- nor human IgG-specific. Importantly, we found a strong negative correlation between the absolute number of IVIg-mobilized plasma cells and time to improve neurological function in both retrospective and prospective studies of Guillain-Barré syndrome (GBS), (r = -0.52, p = 0.0031, n = 30, r = -0.47, p = 0.0028, n = 40, respectively). CONCLUSIONS/SIGNIFICANCE: IVIg promotes immature plasma-cell mobilization in patients with GBS, chronic inflammatory demyelinating polyneuropathy, myasthenia gravis and inflammatory myopathy. Prominent day 7 plasma-cell mobilization is a favourable prognostic marker in patients with GBS receiving IVIg treatment
Exhausted Cytotoxic Control of Epstein-Barr Virus in Human Lupus
Systemic Lupus Erythematosus (SLE) pathology has long been associated with an increased Epstein-Barr Virus (EBV) seropositivity, viremia and cross-reactive serum antibodies specific for both virus and self. It has therefore been postulated that EBV triggers SLE immunopathology, although the mechanism remains elusive. Here, we investigate whether frequent peaks of EBV viral load in SLE patients are a consequence of dysfunctional anti-EBV CD8+ T cell responses. Both inactive and active SLE patients (nâ=â76 and 42, respectively), have significantly elevated EBV viral loads (Pâ=â0.003 and 0.002, respectively) compared to age- and sex-matched healthy controls (nâ=â29). Interestingly, less EBV-specific CD8+ T cells are able to secrete multiple cytokines (IFN-Îł, TNF-α, IL-2 and MIP-1ÎČ) in inactive and active SLE patients compared to controls (Pâ=â0.0003 and 0.0084, respectively). Moreover, EBV-specific CD8+ T cells are also less cytotoxic in SLE patients than in controls (CD107a expression: Pâ=â0.0009, Granzyme B release: Pâ=â0.0001). Importantly, cytomegalovirus (CMV)-specific responses were not found significantly altered in SLE patients. Furthermore, we demonstrate that EBV-specific CD8+ T cell impairment is a consequence of their Programmed Death 1 (PD-1) receptor up-regulation, as blocking this pathway reverses the dysfunctional phenotype. Finally, prospective monitoring of lupus patients revealed that disease flares precede EBV reactivation. In conclusion, EBV-specific CD8+ T cell responses in SLE patients are functionally impaired, but EBV reactivation appears to be an aggravating consequence rather than a cause of SLE immunopathology. We therefore propose that autoimmune B cell activation during flares drives frequent EBV reactivation, which contributes in a vicious circle to the perpetuation of immune activation in SLE patients
An upper limit to the photon fraction in cosmic rays above 10^19 eV from the Pierre Auger Observatory
An upper limit of 16% (at 95% c.l.) is derived for the photon fraction in cosmic rays with energies above 10^19 eV, based on observations of the depth of shower maximum performed with the hybrid detector of the Pierre Auger Observatory. This is the first such limit on photons obtained by observing the fluorescence light profile of air showers. This upper limit confirms and improves on previous results from the Haverah Park and AGASA surface arrays. Additional data recorded with the Auger surface detectors for a subset of the event sample, support the conclusion that a photon origin of the observed events is not favoured
The effect of the geomagnetic field on cosmic ray energy estimates and large scale anisotropy searches on data from the Pierre Auger Observatory
We present a comprehensive study of the influence of the geomagnetic field on
the energy estimation of extensive air showers with a zenith angle smaller than
, detected at the Pierre Auger Observatory. The geomagnetic field
induces an azimuthal modulation of the estimated energy of cosmic rays up to
the ~2% level at large zenith angles. We present a method to account for this
modulation of the reconstructed energy. We analyse the effect of the modulation
on large scale anisotropy searches in the arrival direction distributions of
cosmic rays. At a given energy, the geomagnetic effect is shown to induce a
pseudo-dipolar pattern at the percent level in the declination distribution
that needs to be accounted for.Comment: 20 pages, 14 figure
An upper limit to the photon fraction in cosmic rays above 10^19 eV from the Pierre Auger Observatory
31 pages, 11 figures, 2 tables. Minor changes, appendix expanded, conclusions unchanged; accepted by Astroparticle PhysicsAn upper limit of 16% (at 95% c.l.) is derived for the photon fraction in cosmic rays with energies greater than 10^19 eV, based on observations of the depth of shower maximum performed with the hybrid detector of the Pierre Auger Observatory. This is the first such limit on photons obtained by observing the fluorescence light profile of air showers. This upper limit confirms and improves on previous results from the Haverah Park and AGASA surface arrays. Additional data recorded with the Auger surface detectors for a subset of the event sample, support the conclusion that a photon origin of the observed events is not favored
The Pierre Auger Observatory scaler mode for the study of solar activity modulation of galactic cosmic rays
Since data-taking began in January 2004, the Pierre Auger Observatory has been recording the count rates of low energy secondary cosmic ray particles for the self-calibration of the ground detectors of its surface detector array. After correcting for atmospheric effects, modulations of galactic cosmic rays due to solar activity and transient events are observed. Temporal variations related with the activity of the heliosphere can be determined with high accuracy due to the high total count rates. In this study, the available data are presented together with an analysis focused on the observation of Forbush decreases, where a strong correlation with neutron monitor data is found.K.B. Barber... J.A. Bellido... R.W. Clay... M.J. Cooper... B.R. Dawson... A.E. Herve... V.C. Holmes... J. Sorokin... P. Wahrlich... B.J. Whelan... M.G. Winnick... et al., [for] The Pierre Auger collaboratio