66 research outputs found
Celecoxib as an Adjuvant to Fluvoxamine in Moderate to Severe Obsessive-compulsive Disorder: A Double-blind, Placebo-controlled, Randomized Trial
- Author
- Publication venue
- Publication date
- 01/01/2015
- Field of study
Introduction: A growing body of evidence implicates inflammatory cascades in the pathophysiology of obsessive-compulsive disorder (OCD), making this pathway a target for development of novel treatments. Methods: 50 outpatients with moderate to severe OCD participated in the trial, and underwent 10 weeks of treatment with either celecoxib (200 mg twice daily) or placebo as an adjuvant to fluvoxamine. Participants were investigated using Yale-Brown Obsessive Compulsive Scale (Y-BOCS). The main outcome measure was to assess the efficacy of celecoxib in improving the OCD symptoms. Results: General linear model repeated measures demonstrated significant effect for time � treatment interaction on the Y-BOCS total scores F (1.38, 66.34)=6.91, p=0.005. Kaplan-Meier estimation with log-rank test demonstrated significantly more rapid response in the celecoxib group than the placebo group (p<0.001). There was no significant difference in adverse event frequencies between the groups. Discussion: The results of the current study suggest that celecoxib could be a tolerable and effective adjunctive treatment for more rapid and more satisfying improvements in OCD symptoms. © Georg Thieme Verlag KG Stuttgart, New York
Primary antibody deficiency in a tertiary referral hospital: A 30-year experiment
- Author
- Abolhassani H.
- Afarideh M.
- Aghamohammadi A.
- Ahanchian H.
- Ahmadiafshar A.
- Aleyasin S.
- Amin R.
- Bemanian M.
- Chavoushzadeh Z.
- Cherghi T.
- Faridhosseini R.
- Fayezi A.
- Ghaffari J.
- Ghajar A.
- Gharagozlou M.
- Havaei A.
- Jabbari-Azad F.
- Kalantari N.
- Khazaei H.A.
- Mahdaviani A.
- Masoom S.N.
- Mirminachi B.
- Mirsaeed-Ghazi B.
- Moghtaderi M.
- Mohammadi J.
- Mohammadinejad P.
- Mohammadzadeh I.
- Movahedi M.
- Nabavi M.
- Parvaneh N.
- Pourhamdi S.
- Rezaei N.
- Sadeghi B.
- Sadeghi-Shabestari M.
- Shafiei A.
- Sherkat R.
- Zandieh F.
- Zandkarimi M.
- Publication venue
- Publication date
- 01/01/2015
- Field of study
Background: Primary antibody deficiency (PAD) is the most common group of primary immunodeficiency disorders (PID), with a broad spectrum of clinical features ranging from severe and recurrent infections to asymptomatic disease. Objectives: The current study was performed to evaluate and compare demographic and clinical data in the most common types of PAD. Materials and Methods: We performed a retrospective review of the medical records of all PAD patients with a confirmed diagnosis of common variable immunodeficiency (CVID), hyper IgM syndrome (HIgM), selective IgA deficiency (SIgAD), and X-linked agammaglobulinemia (XLA) who were diagnosed during the last 30 years at the Children�s Medical Center, Tehran, Iran. Results: A total number of 280 cases of PAD (125 CVID, 32 HIgM, 63 SIgAD, and 60 XLA) were enrolled in the study. The median (range) age at the onset of disease in CVID, HIgM, SIgAD, and XLA was 2 (0-46), 0.91 (0-9), 1 (0-26), and 1 (0-10) years, respectively. Gastrointestinal infections were more prevalent in CVID patients, as were central nervous system infections in XLA patients. Autoimmune complications were more prevalent in HIgM patients, malignancies in CVID patients, and allergies in SIgAD patients. The mortality rate for CVID, HIgM, and XLA was 27.2, 28.1, and 25, respectively. No deaths were reported in SIgAD patients. Conclusions: SIgAD patients had the best prognosis. While all PAD patients should be monitored for infectious complications, special attention should be paid to the finding of malignancy and autoimmune disorders in CVID and HIgM patients, respectively. © 2015 Esmon Publicidad
Primary immunodeficiency disorders in Iran: Update and new insights from the third report of the national registry
- Author
- Abolhassani H.
- Aghamohammadi A.
- Ahanchian H.
- Ahmadiafshar A.
- Aleyasin S.
- Amin R.
- Arshi S.
- Atarod L.
- Behmanesh F.
- Bemanian M.H.
- Chavoushzadeh Z.
- Cheraghi T.
- Farid Hosseini R.
- Fayezi A.
- Ghaffari J.
- Gharagozlou M.
- Hedayat E.
- Jabbari-Azad F.
- Javahertrash N.
- Kalantari N.
- Khazaei H.A.
- Mahdaviani A.
- Mansouri M.
- Mirminachi B.
- Mirsaeed-Ghazi B.
- Moghtaderi M.
- Mohammadinejad P.
- Mohammadzadeh I.
- Movahedi M.
- Nabavi M.
- Nadjafi A.
- Parvaneh N.
- Rezaei N.
- Sadeghi-Shabestari M.
- Shafiei A.
- Shakerian B.
- Sharifi B.
- Sherkat R.
- Shirkani A.
- Yousefzadegan S.
- Zandieh F.
- Zandkarimi M.
- Zeiaee V.
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
Background: Primary immunodeficiency disorders (PID) are a group of heterogeneous disorders mainly characterized by severe and recurrent infections and increased susceptibility to malignancies, lymphoproliferative and autoimmune conditions. National registries of PID disorders provide epidemiological data and increase the awareness of medical personnel as well as health care providers. Methods: This study presents the demographic data and clinical manifestations of Iranian PID patients who were diagnosed from March 2006 till the March of 2013 and were registered in Iranian PID Registry (IPIDR) after its second report of 2006. Results: A total number of 731 new PID patients (455 male and 276 female) from 14 medical centers were enrolled in the current study. Predominantly antibody deficiencies were the most common subcategory of PID (32.3 %) and were followed by combined immunodeficiencies (22.3 %), congenital defects of phagocyte number, function, or both (17.4 %), well-defined syndromes with immunodeficiency (17.2 %), autoinflammatory disorders (5.2 %), diseases of immune dysregulation (2.6 %), defects in innate immunity (1.6 %), and complement deficiencies (1.4 %). Severe combined immunodeficiency was the most common disorder (21.1 %). Other prevalent disorders were common variable immunodeficiency (14.9 %), hyper IgE syndrome (7.7 %), and selective IgA deficiency (7.5 %). Conclusions: Registration of Iranian PID patients increased the awareness of medical community of Iran and developed diagnostic and therapeutic techniques across more parts of the country. Further efforts must be taken by increasing the coverage of IPIDR via electronically registration and gradual referral system in order to provide better estimation of PID in Iran and reduce the number of undiagnosed cases. © 2014 Springer Science+Business Media
The B-cell compartment in antibody-deficient infants and young children – developing common variable immunodeficiency or transient immune maturation?
- Author
- AAJM Ven van de
- AL Gervassi
- Aleksandra Szczawinska-Poplonyk
- AM Vale
- B Piatosa
- B Piatosa
- B Piqueras
- C Wehr
- E Vries De
- E Vries De
- EJH Schatorje
- ET Luning Prak
- G Driessen
- H Alachkar
- H Morbach
- Husam Samara
- J Smet
- K Bukowska-Strakova
- K Huck
- K Pieper
- K Warnatz
- K Warnatz
- Katarzyna Tapolska-Jozwiak
- L Yel
- M Al Kindi
- M Aydogan
- M Bemark
- M Burg Van der
- M Duchamp
- M Vodjgani
- MJ Dorsey
- MM Rosado
- N Quamar
- NE Karaca
- P Mohammadinejad
- PL Yong
- S Hokibara
- S Suryani
- TW Bien Le
- TW LeBien
- V Moschese
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
- Author
- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
- Adornetto A.
- Aflaki E.
- Agam G.
- Agarwal A.
- Aggarwal B. B.
- Agnello M.
- Agostinis P.
- Agrewala J. N.
- Agrotis A.
- Aguilar P. V.
- Ahmad S. T.
- Ahmed Z. M.
- Ahumada-Castro U.
- Aits S.
- Aizawa S.
- Akkoc Y.
- Akoumianaki T.
- Akpinar H. A.
- Al-Abd A. M.
- Al-Akra L.
- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
- Alberti S.
- Alcocer-Gomez E.
- Alessandri C.
- Ali M.
- Alim Al-Bari M. A.
- Aliwaini S.
- Alizadeh J.
- Almacellas E.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
- Author
- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
- Acevedo-Arozena A
- Adamopoulos IE
- Adeli K
- Adolph TE
- Adornetto A
- Aflaki E
- Agam G
- Agarwal A
- Aggarwal BB
- Agnello M
- Agostinis P
- Agrewala JN
- Agrotis A
- Aguilar PV
- Ahmad ST
- Ahmed ZM
- Ahumada-Castro U
- Aits S
- Aizawa S
- Akkoc Y
- Akoumianaki T
- Akpinar HA
- Al-Abd AM
- Al-Akra L
- Al-Gharaibeh A
- Alaoui-Jamali MA
- Alberti S
- Alcocer-Gómez E
- Alessandri C
- Ali M
- Alim Al-Bari MA
- Aliwaini S
- Alizadeh J
- Almacellas E
- Almasan A
- Alonso A
- Alonso GD
- Altan-Bonnet N
- Altieri DC
- Alves da Costa C
- Alves S
- Alzaharna MM
- Amadio M
- Amantini C
- Amaral C
- Ambrosio S
- Amer AO
- Ammanathan V
- An Z
- Andersen SU
- Andrabi SA
- Andrade-Silva M
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- Angelini S
- Ann D
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- Artero R
- Arévalo M-A
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- Aschner M
- Ashrafizadeh M
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- Atanasov AG
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- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Modeling the prevalence of immunodeficiency-associated long-term vaccine-derived poliovirus excretors and the potential benefits of antiviral drugs
- Author
- A Bellmunt
- AA Bousfiha
- AS DeVries
- AY Joshi
- B Gathmann
- C Burns
- CA MacLennan
- Centers for Disease Control and Prevention
- DA Kalkowska
- E Savilahti
- FO MacCallum
- H Abolhassani
- H Al-Hello
- H Chapel
- H Triki
- J Guo
- J Martin
- J Martín
- JM Boyle
- JP Alexander Jr
- JS Orange
- Kimberly M. Thompson
- KM Thompson
- KM Thompson
- KM Thompson
- L Fiore
- L Li
- LN Alexander
- M Hara
- M Tiongco-Recto
- MA McKinlay
- Mark A. Pallansch
- N Driss
- N Driss
- N Khetsuriani
- NA Halsey
- National Research Council
- NM Galal
- OM Kew
- P Minor
- P Mohammadinejad
- P Más Lago
- PF Yong
- R Silva de
- Radboud J. Duintjer Tebbens
- RJ Duintjer Tebbens
- RJ Duintjer Tebbens
- RJ Duintjer Tebbens
- RJ Duintjer Tebbens
- RJ Duintjer Tebbens
- RT Chen
- S Shahmahmoodi
- T Hovi
- T Hovi
- V Modell
- V Modell
- World Health Organization
- World Health Organization
- World Health Organization Collaborative Study Group on Oral and Inactivated Poliovirus Vaccines
- WR Dowdle
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Combined immunodeficiency (CVID and CD4 lymphopenia) is associated with a high risk of malignancy among adults with primary immune deficiency
- Publication venue
- 'Wiley'
- Publication date
- Field of study
Paving the road toward exploiting the therapeutic effects of ginsenosides: an emphasis on autophagy and endoplasmic reticulum stress
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/04/2021
- Field of study
Programmed cell death processes such as apoptosis and autophagy strongly contribute to the onset and progression of cancer. Along with these lines, modulation of cell death mechanisms to combat cancer cells and elimination of resistance to apoptosis is of great interest. It appears that modulation of autophagy and endoplasmic reticulum (ER) stress with specific agents would be beneficial in the treatment of several disorders. Interestingly, it has been suggested that herbal natural products may be suitable candidates for the modulation of these processes due to few side effects and significant therapeutic potential. Ginsenosides are derivatives of ginseng and exert modulatory effects on the molecular mechanisms associated with autophagy and ER stress. Ginsenosides act as smart phytochemicals that confer their effects by up-regulating ATG proteins and converting LC3-I to -II, which results in maturation of autophagosomes. Not only do ginsenosides promote autophagy but they also possess protective and therapeutic properties due to their capacity to modulate ER stress and up- and down-regulate and/or dephosphorylate UPR transducers such as IRE1, PERK, and ATF6. Thus, it would appear that ginsenosides are promising agents to potentially restore tissue malfunction and possibly eliminate cancer
Curcumin delivery mediated by bio-based nanoparticles: A review
- Author
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Todays, nano-pharmaceutics is emerging as an important field of science to develop and improve efficacy of different drugs. Although nutraceuticals are currently being utilized in the prevention and treatment of various chronic diseases such as cancers, a number of them have displayed issues associated with their solubility, bioavailability, and bio-degradability. In the present review, we focus on curcumin, an important and widely used polyphenol, with diverse pharmacological activities such as anti-inflammatory, anti-carcinogenic, anti-viral, etc. Notwithstanding, it also exhibits poor solubility and bioavailability that may compromise its clinical application to a great extent. Therefore, the manipulation and encapsulation of curcumin into a nanocarrier formulation can overcome these major drawbacks and potentially may lead to a far superior therapeutic efficacy. Among different types of nanocarriers, biological and biopolymer carriers have attracted a significant attention due to their pleiotropic features. Thus, in the present review, the potential protective and therapeutic applications of curcumin, as well as different types of bio-nanocarriers, which can be used to deliver curcumin effectively to the different target sites will be discussed. © 2020 by the authors
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