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Article ; Online: Antibody Therapy for COVID-19: Categories, Pros, and Cons.

Zare Marzouni, Hadi / Rahbar, Marjan / Seddighi, Nazanin / Nabizadeh, Mohsen / Meidaninikjeh, Sepideh / Sabouni, Nasim

2022 Volume 35, Issue 8, Page(s) 517–528

Abstract: COVID-19 is a life-threatening respiratory disease triggered by severe acute respiratory syndrome coronavirus 2 ( ...

Abstract	COVID-19 is a life-threatening respiratory disease triggered by severe acute respiratory syndrome coronavirus 2 (
MeSH term(s)	Antibodies, Viral ; Antiviral Agents/therapeutic use ; COVID-19/therapy ; Humans ; Immunization, Passive ; Pharmaceutical Preparations ; SARS-CoV-2
Chemical Substances	Antibodies, Viral ; Antiviral Agents ; Pharmaceutical Preparations
Language	English
Publishing date	2022-10-06
Publishing country	United States
Document type	Journal Article ; Review
ZDB-ID	639075-4
ISSN	1557-8976 ; 0882-8245
ISSN (online)	1557-8976
ISSN	0882-8245
DOI	10.1089/vim.2021.0160
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Article ; Online: Interleukin-1

Mardi, Amirhossein / Meidaninikjeh, Sepideh / Nikfarjam, Sepideh / Majidi Zolbanin, Naime / Jafari, Reza

Viral immunology

2021 Volume 34, Issue 10, Page(s) 679–688

Abstract: The newfound coronavirus disease 2019 (COVID-19), initiated by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is an international public health concern, threatening the lives of millions of people worldwide. The virus seems to have a ... ...

Abstract	The newfound coronavirus disease 2019 (COVID-19), initiated by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is an international public health concern, threatening the lives of millions of people worldwide. The virus seems to have a propensity to infect older males, especially those with underlying diseases. The cytokine storm following hyperactivated immune responses due to SARS-CoV-2 infection is probably the crucial source of severe pneumonia that leads to acute lung injury, systemic inflammatory response syndrome, or acute respiratory distress syndrome, and finally multiple organ dysfunction syndromes, as well as death in many cases. Several studies revealed that interleukin (IL)-1
MeSH term(s)	Acute Lung Injury/drug therapy ; Acute Lung Injury/immunology ; Acute Lung Injury/pathology ; COVID-19/drug therapy ; COVID-19/immunology ; COVID-19/mortality ; COVID-19/pathology ; Cytokine Release Syndrome/drug therapy ; Cytokine Release Syndrome/immunology ; Cytokine Release Syndrome/pathology ; Humans ; Interleukin-1/antagonists & inhibitors ; Interleukin-1/immunology ; Multiple Organ Failure/drug therapy ; Multiple Organ Failure/immunology ; Multiple Organ Failure/pathology ; Respiratory Distress Syndrome/drug therapy ; Respiratory Distress Syndrome/immunology ; Respiratory Distress Syndrome/pathology ; SARS-CoV-2/immunology ; SARS-CoV-2/pathogenicity
Chemical Substances	Interleukin-1
Language	English
Publishing date	2021-12-08
Publishing country	United States
Document type	Journal Article ; Review
ZDB-ID	639075-4
ISSN	1557-8976 ; 0882-8245
ISSN (online)	1557-8976
ISSN	0882-8245
DOI	10.1089/vim.2021.0071
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Article ; Online: Role of curcumin and its nanoformulations in the treatment of neurological diseases through the effects on stem cells.

Sabouni, Nasim / Marzouni, Hadi Zare / Palizban, Sepideh / Meidaninikjeh, Sepideh / Kesharwani, Prashant / Jamialahmadi, Tannaz / Sahebkar, Amirhossein

Journal of drug targeting

2022 Volume 31, Issue 3, Page(s) 243–260

Abstract: Curcumin from turmeric is a natural phenolic compound with a promising potential to regulate fundamental processes involved in neurological diseases, including inflammation, oxidative stress, protein aggregation, and apoptosis at the molecular level. In ... ...

Abstract	Curcumin from turmeric is a natural phenolic compound with a promising potential to regulate fundamental processes involved in neurological diseases, including inflammation, oxidative stress, protein aggregation, and apoptosis at the molecular level. In this regard, employing nanoformulation can improve curcumin efficiency by reducing its limitations, such as low bioavailability. Besides curcumin, growing data suggest that stem cells are a noteworthy candidate for neurodegenerative disorders therapy due to their anti-inflammatory, anti-oxidative, and neuronal-differentiation properties, which result in neuroprotection. Curcumin and stem cells have similar neurogenic features and can be co-administered in a cell-drug delivery system to achieve better combination therapeutic outcomes for neurological diseases. Based on the evidence, curcumin can induce the neuroprotective activity of stem cells by modulating their related signalling pathways. The present review is about the role of curcumin and its nanoformulations in the improvement of neurological diseases alone and through the effect on different categories of stem cells by discussing the underlying mechanisms to provide a roadmap for future investigations.
MeSH term(s)	Humans ; Curcumin/pharmacology ; Curcumin/therapeutic use ; Oxidative Stress ; Neurodegenerative Diseases/drug therapy ; Neurodegenerative Diseases/metabolism ; Antioxidants/pharmacology ; Stem Cells/metabolism
Chemical Substances	Curcumin (IT942ZTH98) ; Antioxidants
Language	English
Publishing date	2022-11-20
Publishing country	England
Document type	Review ; Journal Article
ZDB-ID	1187110-6
ISSN	1029-2330 ; 1061-186X
ISSN (online)	1029-2330
ISSN	1061-186X
DOI	10.1080/1061186X.2022.2141755
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Article: Monocytes and macrophages in COVID-19: Friends and foes

Meidaninikjeh, Sepideh / Sabouni, Nasim / Marzouni, Hadi Zare / Bengar, Sajad / Khalili, Ahmad / Jafari, Reza

Life sciences. 2021 Mar. 15, v. 269

2021

Abstract: The COVID-19 is a novel infectious disease caused by SARS-CoV-2 and is known as a pandemic emergency that has led to a high rate of mortality throughout the world. Evidence has indicated that hyperinflammatory responses triggered by SARS-CoV-2 are the ... ...

Abstract	The COVID-19 is a novel infectious disease caused by SARS-CoV-2 and is known as a pandemic emergency that has led to a high rate of mortality throughout the world. Evidence has indicated that hyperinflammatory responses triggered by SARS-CoV-2 are the main cause of pathogenicity in the severe cases of patients who have died during the current viral disease. Monocytes and macrophages as the most important cells of the innate arm of the immune system play a substantial part in the body's defense against viral infections. They mainly respond to the microbial antigens by producing inflammatory mediators to remove pathogens and repair tissue injury. Nevertheless, aberrant alterations in their function such as cytokine storm can be so harmful to the host in the acute respiratory distress syndrome cases caused by SARS-CoV-2. Moreover, inflammatory responses stimulated by SARS-CoV-2 have affected the other vital organs of the body including the heart. As cardiovascular complications in COVID-19 patients have been reported in several studies. During the infection, monocytes and macrophages may be involved in the hypersensitive and exacerbated reactions that contribute to the tissue damage, especially lung injury resulted in its dysfunction and respiratory disorder. In this review, we discuss both advantageous and disadvantageous about the pathological potential of monocytes and macrophages during the infection of SARS-CoV-2 to clarify their mutual effects on immune processing as a fist line defender in the current disease.
Keywords	COVID-19 infection ; Severe acute respiratory syndrome coronavirus 2 ; acute respiratory distress syndrome ; cytokines ; heart ; lungs ; macrophages ; monocytes ; mortality ; pandemic ; pathogenicity
Language	English
Dates of publication	2021-0315
Publishing place	Elsevier Inc.
Document type	Article
Note	NAL-light
ZDB-ID	3378-9
ISSN	1879-0631 ; 0024-3205
ISSN (online)	1879-0631
ISSN	0024-3205
DOI	10.1016/j.lfs.2020.119010
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Monocytes and macrophages in COVID-19: Friends and foes.

Meidaninikjeh, Sepideh / Sabouni, Nasim / Marzouni, Hadi Zare / Bengar, Sajad / Khalili, Ahmad / Jafari, Reza

Life sciences

2021 Volume 269, Page(s) 119010

Abstract	The COVID-19 is a novel infectious disease caused by SARS-CoV-2 and is known as a pandemic emergency that has led to a high rate of mortality throughout the world. Evidence has indicated that hyperinflammatory responses triggered by SARS-CoV-2 are the main cause of pathogenicity in the severe cases of patients who have died during the current viral disease. Monocytes and macrophages as the most important cells of the innate arm of the immune system play a substantial part in the body's defense against viral infections. They mainly respond to the microbial antigens by producing inflammatory mediators to remove pathogens and repair tissue injury. Nevertheless, aberrant alterations in their function such as cytokine storm can be so harmful to the host in the acute respiratory distress syndrome cases caused by SARS-CoV-2. Moreover, inflammatory responses stimulated by SARS-CoV-2 have affected the other vital organs of the body including the heart. As cardiovascular complications in COVID-19 patients have been reported in several studies. During the infection, monocytes and macrophages may be involved in the hypersensitive and exacerbated reactions that contribute to the tissue damage, especially lung injury resulted in its dysfunction and respiratory disorder. In this review, we discuss both advantageous and disadvantageous about the pathological potential of monocytes and macrophages during the infection of SARS-CoV-2 to clarify their mutual effects on immune processing as a fist line defender in the current disease.
MeSH term(s)	Animals ; COVID-19/complications ; COVID-19/immunology ; COVID-19/virology ; Cytokine Release Syndrome/immunology ; Cytokine Release Syndrome/virology ; Humans ; Macrophages/immunology ; Monocytes/immunology ; Respiratory Distress Syndrome/immunology ; Respiratory Distress Syndrome/virology ; SARS-CoV-2/isolation & purification
Language	English
Publishing date	2021-01-14
Publishing country	Netherlands
Document type	Journal Article ; Review
ZDB-ID	3378-9
ISSN	1879-0631 ; 0024-3205
ISSN (online)	1879-0631
ISSN	0024-3205
DOI	10.1016/j.lfs.2020.119010
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Article: The protection quest is a primary key to sharing the neutralizing antibody response to cover against all emerging VOCs based on BIV1-CovIran studies.

Shafaati, Maryam / Bagherzadeh, Kowsar / Lotfinia, Majid / Karimi, Hesam / Teimoori, Ali / Razazian, Mehdi / Meidaninikjeh, Sepideh / Hosseini, Hamed / Jamshidi, Hamid Reza / Jalili, Hasan / Abdoli, Asghar

Heliyon

2023 Volume 9, Issue 3, Page(s) e14108

Abstract: Over time, the antigenic evolution of emerging variants of SARS-CoV-2 has demanded the development of potential protective vaccines. Administration of additional doses of current vaccines based on the WT spike protein may boost immunity, but their ... ...

Abstract	Over time, the antigenic evolution of emerging variants of SARS-CoV-2 has demanded the development of potential protective vaccines. Administration of additional doses of current vaccines based on the WT spike protein may boost immunity, but their effectiveness has dwindled for patients with more recent variants. Here, we studied the neutralization activity of post-WT strain-based vaccination and a structural simulation
Language	English
Publishing date	2023-02-26
Publishing country	England
Document type	Journal Article
ZDB-ID	2835763-2
ISSN	2405-8440
ISSN	2405-8440
DOI	10.1016/j.heliyon.2023.e14108
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: SARS-CoV-2 and Guillain-Barré Syndrome: Lessons from Viral Infections.

Meidaninikjeh, Sepideh / Sabouni, Nasim / Taheri, Mahdie / Borjkhani, Mahdis / Bengar, Sajad / Majidi Zolbanin, Naime / Khalili, Ahmad / Jafari, Reza

Viral immunology

2022 Volume 35, Issue 6, Page(s) 404–417

Abstract: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is responsible for the COVID-19 pandemic. COVID-19 has a broad clinical spectrum from asymptomatic patients to multiorgan dysfunction and septic shock. Most of the common symptoms of COVID-19 ... ...

Abstract	Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is responsible for the COVID-19 pandemic. COVID-19 has a broad clinical spectrum from asymptomatic patients to multiorgan dysfunction and septic shock. Most of the common symptoms of COVID-19 are classified as respiratory disorders, but some reports show neurological involvements. During the COVID-19 pandemic, a case series of neurological complications, such as Guillain-Barré syndrome (GBS), were reported. GBS is a neuroimmune disorder with acute inflammatory radicular polyneuropathy in different parts of the peripheral nerve. Some studies have reported GBS as an inflammatory neuropathy related to various viral infections, such as cytomegalovirus (CMV), Epstein-Barr Virus (EBV), herpes simplex virus (HSV), human immunodeficiency virus (HIV), influenza, and Zika virus. There are some immunomodulation approaches for the management of GBS. Studies have evaluated the effects of the various therapeutic approaches, including intravenous immunoglobulin (IVIG), plasma exchange (PE), complement inhibitors, and corticosteroids to regulate overactivation of immune responses during GBS in experimental and clinical studies. In this regard, the possible association between GBS and SARS-CoV-2 infection during the outbreak of the current pandemic and also the mentioned therapeutic approaches were reviewed.
MeSH term(s)	COVID-19/complications ; Epstein-Barr Virus Infections/complications ; Guillain-Barre Syndrome/diagnosis ; Guillain-Barre Syndrome/epidemiology ; Guillain-Barre Syndrome/therapy ; Herpesvirus 4, Human ; Humans ; Pandemics ; SARS-CoV-2 ; Zika Virus ; Zika Virus Infection
Language	English
Publishing date	2022-06-29
Publishing country	United States
Document type	Journal Article ; Review
ZDB-ID	639075-4
ISSN	1557-8976 ; 0882-8245
ISSN (online)	1557-8976
ISSN	0882-8245
DOI	10.1089/vim.2021.0187
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Article ; Online: The protection quest is a primary key to sharing the neutralizing antibody response to cover against all emerging VOCs based on BIV1-CovIran studies

Heliyon. 2023 Mar., v. 9, no. 3 p.e14108-

2023

Abstract	Over time, the antigenic evolution of emerging variants of SARS-CoV-2 has demanded the development of potential protective vaccines. Administration of additional doses of current vaccines based on the WT spike protein may boost immunity, but their effectiveness has dwindled for patients with more recent variants. Here, we studied the neutralization activity of post-WT strain-based vaccination and a structural simulation in-silico based on the interactions of the RBD-hACE2 as the key to initiating infection among the VOCs of SARS-CoV-2. Our data display shows that WT sera showed a markedly greater reduction in Delta and Omicron, suggesting that the Wuhan-based vaccines may be more susceptible to breakthrough and new VOCs. According to the MD simulation, mutations of Omicron result in a significant change in the variant charge distribution throughout the binding interface that consequently alters the critical interface electrostatic potential in comparison to other variants. This observation provides new insights into immunization policy and next-generation vaccine development.
Keywords	Severe acute respiratory syndrome coronavirus 2 ; antibody formation ; computer simulation ; issues and policy ; neutralization ; vaccination ; vaccine development ; SARS-CoV-2 ; Variants of concern ; Neutralizing antibody ; Molecular dynamic simulations ; Vaccine
Language	English
Dates of publication	2023-03
Publishing place	Elsevier Ltd
Document type	Article ; Online
Note	Use and reproduction
ZDB-ID	2835763-2
ISSN	2405-8440
ISSN	2405-8440
DOI	10.1016/j.heliyon.2023.e14108
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: The protection quest is a primary key to sharing the neutralizing antibody response to cover against all emerging VOCs based on BIV1-CovIran studies

Maryam Shafaati / Kowsar Bagherzadeh / Majid Lotfinia / Hesam Karimi / Ali Teimoori / Mehdi Razazian / Sepideh Meidaninikjeh / Hamed Hosseini / Hamid Reza Jamshidi / Hasan Jalili / Asghar Abdoli

Heliyon, Vol 9, Iss 3, Pp e14108- (2023)

2023

Abstract	Over time, the antigenic evolution of emerging variants of SARS-CoV-2 has demanded the development of potential protective vaccines. Administration of additional doses of current vaccines based on the WT spike protein may boost immunity, but their effectiveness has dwindled for patients with more recent variants. Here, we studied the neutralization activity of post-WT strain-based vaccination and a structural simulation in-silico based on the interactions of the RBD-hACE2 as the key to initiating infection among the VOCs of SARS-CoV-2. Our data display shows that WT sera showed a markedly greater reduction in Delta and Omicron, suggesting that the Wuhan-based vaccines may be more susceptible to breakthrough and new VOCs. According to the MD simulation, mutations of Omicron result in a significant change in the variant charge distribution throughout the binding interface that consequently alters the critical interface electrostatic potential in comparison to other variants. This observation provides new insights into immunization policy and next-generation vaccine development.
Keywords	SARS-CoV-2 ; Variants of concern ; Neutralizing antibody ; Molecular dynamic simulations ; Vaccine ; Science (General) ; Q1-390 ; Social sciences (General) ; H1-99
Language	English
Publishing date	2023-03-01T00:00:00Z
Publisher	Elsevier
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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Article ; Online: A comparative study of various methods for detection of IL28B rs12979860 in chronic hepatitis C.

Monavari, Seyed Hamidreza / Fateh, Roohollah / Vaziri, Farzam / Rahimi Jamnani, Fatemeh / Anvari, Enayat / Sadeghi, Farzin / Afrough, Parviz / Behrouzi, Ava / Sakhaee, Fatemeh / Meidaninikjeh, Sepideh / Mollaie, Hamidreza / Hadizadeh Tasbiti, Alireza / Yari, Shamsi / Sadeghi, Maryam / Fateh, Abolfazl / Siadat, Seyed Davar

Scandinavian journal of clinical and laboratory investigation

2017 Volume 77, Issue 4, Page(s) 247–252

Abstract: Interleukin-28B (IL28B) single-nucleotide polymorphisms (SNPs) constitute important host-related factors influencing the response rate to Hepatitis C virus (HCV) standard antiviral therapy. In the last few years, several new technologies for SNP ... ...

Abstract	Interleukin-28B (IL28B) single-nucleotide polymorphisms (SNPs) constitute important host-related factors influencing the response rate to Hepatitis C virus (HCV) standard antiviral therapy. In the last few years, several new technologies for SNP detection have been developed. However, the sensitivity and specificity of various methods are different and needs evaluation. Five different methods (resolution melting curve [RMC], polymerase chain reaction-restriction fragment length polymorphism [PCR-RFLP], PCR-sequencing analysis, amplification refractory mutation system [ARMS], and zip nucleic acid probe-based real-time PCR [ZNA]) were developed for genotyping rs12979860 associated with IL28B. In this study, limit of detection (LD), costs and turnaround time of these methods were compared in 350 subjects. As for IL28B rs12979860 polymorphisms, 348/350 (99.4%) samples were consistent among the five methods, while results for 2/350 (0.57%) samples were concordant by ZNAs and PCR-sequencing, and discordant by other methods. Without considering the cost of DNA extraction, the price of each reaction for ARMS-PCR, RMC, PCR-RFLP, ZNA and PCR-sequencing were respectively: US$3.10, US$5.0, US$5.50, US$8.50 and US$17.0. RMC was the fastest method, while the ZNA method was easy to use, reliable and effective. Lower LD was determined to be 50-60 copies/μL for the PCR-RFLP, RMC and ARMS-PCR assays; whilst ZNA assay was able to detect 2-3 copies/μL. In conclusion, in the current study, all four methods are suitable for IL28B rs12979860 genotyping, but the ZNA assay can be a reliable tool. Due to its lower LD for SNP identification, this method is better than others for detecting this type of polymorphism.
MeSH term(s)	Genotype ; Hepatitis C/genetics ; Hepatitis C, Chronic/genetics ; Humans ; Interferons ; Interleukins/genetics ; Limit of Detection ; Polymorphism, Restriction Fragment Length ; Polymorphism, Single Nucleotide ; Real-Time Polymerase Chain Reaction/economics
Chemical Substances	interferon-lambda, human ; Interleukins ; Interferons (9008-11-1)
Language	English
Publishing date	2017-03-10
Publishing country	England
Document type	Comparative Study ; Journal Article
ZDB-ID	3150-1
ISSN	1502-7686 ; 0036-5513
ISSN (online)	1502-7686
ISSN	0036-5513
DOI	10.1080/00365513.2017.1299207
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