ORIGINAL_ARTICLE
Brucella abortus L7/L12 Recombinant Protein Induces Strong Th1 Response in Acute Brucellosis Patients
Background: Because of high morbidity of the brucellosis in humans and the potential use of the microorganism as an agent of biologic warfare, protection of effective vaccines and specific diagnostic reagents become necessary to eradicate brucellosis. Objective: In this study we aimed to investigate the cytokine responses and changes in peripheral blood lymphocyte subgroups of acute brucellosis patients in response to L7/L12 and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) recombinant proteins derived from Brucella abortus. Methods: levels of IFN-γ, IL-4 and IL-10 secreted from PBMCs of 25 acute brucellosis patients and 15 healthy controls, stimulated with Phytohemagglutinin (PHA), L7/L12 or GAPDH were measured by ELISA. Furthermore alterations in lymphocyte subgroups in response to these Brucella antigens were determined by flow cytometry. Results: Extracellular IFN-γ levels were found to be elevated after stimulation with L7/L12 in patients with acute brucellosis, whereas no significant changes were found in IL-4 and IL-10 levels. Similar data was also obtained with GAPDH, but the stimulation of IFN-γ production was not observed in all patients and was not as strong as that observed for L7/L12. Moreover, when the distribution of lymphocytes subgroups (CD3+, CD3+CD4+, CD3+CD8+, CD4+CD25+, CD3+CD69+ and CD3+CD152+) was evaluated, it was found that the stimulation with L7/L12 and GAPDH only led to an increase in the percentage of CD3+CD69+ lymphocytes. Conclusion: These data indicate that Brucella abortus L7/L12 or GAPDH induce a Th1 type immune response in acute brucellosis patients. Additionally, these recombinant proteins, especially L7/L12, may be used in new vaccine preparations and diagnostic tests.
https://iji.sums.ac.ir/article_17050_25ad85c56c0ce05cefa1fa7b5d2387e0.pdf
2010-09-01
132
141
Brucellosis
Cytokine
Recombinant Proteins
T Lymphocytes
Esra
Kazak
1
Department of Infectious Diseases and Clinical Microbiology, Uludağ University Faculty of Medicine, Bursa, Türkiye
AUTHOR
Sergio
Costa Oliveria
2
Department of Biochemistry and Immunology, Federal University of Minas Gerais, Brazil
AUTHOR
Güher
Goral
3
Department of Medical Microbiology, Immunology Unit, Uludağ University Faculty of Medicine, Bursa, Türkiye
AUTHOR
Halis
Akalin
4
Department of Infectious Diseases and Clinical Microbiology, Uludağ University Faculty of Medicine, Bursa, Türkiye
AUTHOR
Emel
Yilmaz
5
Department of Infectious Diseases and Clinical Microbiology, Uludağ University Faculty of Medicine, Bursa, Türkiye
AUTHOR
Yasemin
Heper
6
Department of Infectious Diseases and Clinical Microbiology, Uludağ University Faculty of Medicine, Bursa, Türkiye
AUTHOR
Haluk
Barbaros Oral
oralb@uludag.edu.tr
7
Department of Medical Microbiology, Immunology Unit, Uludağ University Faculty of Medicine, Bursa, Türkiye
LEAD_AUTHOR
ORIGINAL_ARTICLE
Candida albicans Structural and Secreted Proteins Modulate CD4/CD8 Ratio in Tumor Infiltrating Lymphocytes of Spontaneous Adenocarcinoma Bearing Mice
Background: Candida albicans is one of the most important opportunistic pathogens that suppress immunologic mechanisms of the host. It is speculated that structural and secretory proteins of C. albicans have immunomodulatory effects in cancer. Objective: To evaluate the effects of C. albicans structural and secreted proteins on intratumoral CD4/CD8 ratio as well as the survival rate in BALB/c tumor model. Methods: Structural and secretory proteins from C. albicans were isolated and examined for their effects on tumor growth and survival of adenocarcinoma bearing mice. Results: The results indicated that in mice treated with C. albicans structural protein, the survival rate significantly decreased compared with the control groups. Also, mice treated with secretory proteins showed a decrease in survival rate but it was not statistically significant (p>0.05). Investigating the frequency of tumor infiltrated CD4+ and CD8+ T lymphocytes indicated that the percentages of tumor infiltrated CD4+ T lymphocytes in response to structural and secreted proteins were higher compared to the control groups. Conclusion: Our study suggests that C. albicans structural and secreted proteins modulate intratumor T lymphocyte infiltration.
https://iji.sums.ac.ir/article_17051_b02369f7b5b77a151aaf9a82f6e7f545.pdf
2010-09-01
142
149
candida albicans
Lymphocytes
Spontaneous Adenocarcinoma
Structural Proteins
Secreted Proteins
Marzieh
Holakuyee
1
Department of Immunology, Pasteur Institute of Iran
AUTHOR
Mohammad Hossein
Yadegari
yadegarm@modares.ac.ir
2
Department of Medical Mycology
LEAD_AUTHOR
Zuhair Mohammad
Hassan
3
Department of Immunology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran
AUTHOR
Mansour
Bayat
4
Department of Medical and Veterinary Mycology, Faculty of Specialized Veterinary Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran
AUTHOR
Ariyo Shahin
Jafari
5
Department of Medical and Veterinary Mycology, Faculty of Specialized Veterinary Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran
AUTHOR
Mohsen
Abolhassani
6
Department of Immunology, Pasteur Institute of Iran
AUTHOR
Abbas
Ali Amini
7
BuAli Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran
AUTHOR
Mehdi
Mahdavi
8
Department of Immunology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran
AUTHOR
ORIGINAL_ARTICLE
The Use of Crude Plasmodium falciparum Antigens for Comparison of Antibody Responses in Patients with Mild Malaria vs. Cerebral Malaria
Background: Cerebral malaria (CM) is one of the major causes of death in African populations infected with Plasmodium falciparum. Only 1% of infected subjects develop CM. The reasons for these differences are not fully understood, but it is likely that the host humoral response against blood-stage antigens plays a role in protection from malaria, although the precise targets and mechanisms mediating immunity remain unclear. Objective: The purpose of this study was to distinguish between defined P. falciparum- specific Ab response patterns in patients presenting with mild malaria (MM) vs. CM. Methods: We used a panel of P. falciparum conserved antigens including crude blood-stage extracts schizont, merozoite and parasitised erythrocyte membranes and MSP-1p19, PfEB200, R23 and GST-5 recombinant antigens in a retrospective casecontrol study of symptomatic adults, one group presenting confirmed CM without fatal outcome and another group with MM. We further matched P. falciparum-specific Ab responses with those from individuals living in an endemic setting known to have protective immunity and considered them as “immune control” subjects (IC). Total IgG, IgM and IgG subclass Ab responses were determined using ELISA method. Results: Substantial Ab responses were found in symptomatic patients, significantly lower than the “immune control” subjects, and with a limited quantitative difference between MM versus CM. Interestingly, asynchronous IgM response was evidenced in CM contrary to MM. Conclusion: Our results suggest that the contribution of an efficient IgG response against parasite multiplication is of importance in the evolution towards CM manifestation without fatal outcome and deserves further analysis for vaccine candidates.
https://iji.sums.ac.ir/article_17052_9b186ac857ac83addfaafbce24eabb63.pdf
2010-09-01
150
161
Antibody Response
Cerebral Malaria
Non-Complicated Malaria
Plasmodium falciparum
Babacar
Mbengue
1
Laboratoire d'Immunologie, Faculté de Médecine, de Pharmacie et d’Odontostomatologie, Université Cheikh Anta Diop de Dakar, BP 5005, Sénégal
AUTHOR
Birahim
Niang
2
Hôpital Principal, Service de Réanimation, Dakar, Séné- gal,
AUTHOR
Bacary
Diatta
3
Hôpital Principal, Service de Réanimation, Dakar, Séné- gal,
AUTHOR
Adama
Tali
4
Unité d'Immunologie, Institut Pasteur, Dakar, Sénégal
AUTHOR
Olivier
Garraud
5
GIMAP – EA 3064, Faculty of Medicine, University of Saint-Etienne, France
AUTHOR
Ronald
Perraut
6
Institut Pasteur, 28 rue du Dr Roux, 75015 Paris, France
AUTHOR
Alioune
Dieye
alioune.dieye@ucad.edu.sn
7
Laboratoire d'Immunologie, Faculté de Médecine, de Pharmacie et d’Odontostomatologie, Université Cheikh Anta Diop de Dakar, BP 5005, Sénégal
LEAD_AUTHOR
ORIGINAL_ARTICLE
Characterization of Immune Responses Induced by Combined Clade-A HIV-1 Recombinant Adenovectors in Mice
Background: Numerous evidences indicate that in some HIV-1 positive patients, the humoral and cellular immune responses are induced against HIV-1 proteins and this is inversely related to the progress of infection. Objective: The aim of this study was the evaluation of the Adenovectors containing HIV genes in induction of immune responses in mice. Methods: The HIV-1 genes including gag p24, rev, nef and exon-1 of tat were amplified from HIV-1 RNA (clade-A). The cDNA of each gene was cloned into a transfer vector. The transfer vector was then co-transformed into E. coli strain BJ5183 together with pAdenovector ΔE1/E3. The recombinant adenoviral construct was transfected into QBI-293A cells. Recombinant viruses were purified and titrated on 293 cell plates. Expression of transgenes was evaluated using western blotting. Then 1012 viral particles were injected into 15 groups of 5 mice and all patterns of combination of these 4 HIV-1 genes were evaluated. After 2 weeks, humoral and cellular immune responses were evaluated using ELISA, cell proliferation and ELISpot (IL-2, IL-4 and IFN-γ) assays, consecutively. Results: It was demonstrated that each gene was expressed. The response targets were mostly toward Th1, though several Th2 responses were also observed. Single injection in our study induced a good cellular response but the humoral responses were not as strong as the cellular ones. Conclusion: Considering and comparing all results and evaluating the various possible interactions revealed that simultaneous injection of tat and gag has enhanced the humoral and cellular responses.
https://iji.sums.ac.ir/article_17053_a56798beda5e895af717a769b7188892.pdf
2010-09-01
162
176
Adenovector
Cellular Responses
HIV Vaccine
Humoral Immune Responses
Sayeed
Bayanolhagh
1
Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University
AUTHOR
Mahtab
Alinezhad
2
Research and Development Complex, Pasteur Institute of Iran
AUTHOR
Kooroosh
Kamali
3
Department of Epidemiology and Biostatics, Tehran University of Medical Sciences
AUTHOR
Maryam
Foroughi
4
Iranian Research Center for HIV/AIDS, Tehran University of Medical Sciences
AUTHOR
Hamid Reza
Khorram Khorshid
5
Genetic Research Centre, University of Social Welfare and Rehabilitation Sciences
AUTHOR
Minoo
Mohraz
6
Iranian Research Center for HIV/AIDS, Tehran University of Medical Sciences
AUTHOR
Fereidoun
Mahboudi
mahboudi@pasteur.ac.ir
7
Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran
AUTHOR
Ali Akbar
Pourfathollah
pourfa@modares.ac.ir
8
Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University
LEAD_AUTHOR
ORIGINAL_ARTICLE
Expansion of CD4+CD25+FoxP3+ Regulatory T Cells in Chronic Hepatitis C Virus Infection
Background: Regulatory T cells (Tregs) have been involved in impaired immunity and may have a pivotal role in persistence of viral infections. Objective: To develop a simple and reliable in-house three color flow cytometery of peripheral blood to understand the role of HCV infection in the increase of Tregs. Methods: The level of naturally occurring CD4+CD25+FoxP3+ regulatory T cells (nTregs) in 20 chronically infected with hepatitis C virus (HCV) patients was compared to those of 15 healthy individuals by flowcytometry. In a different approach we performed permeabilization and intracellular staining before surface staining which allows the preservation of the surface molecules in the combined detection process and results in the normal frequency of nTregs in blood. Results: Using the optimized method, it was shown that a significantly higher proportion of nTregs in the total CD4+ T cell population was seen in the peripheral blood of chronic HCV patients (0.83 ± 0.21%, p=0.05) as compared to controls (0.26 ± 0.1, p=0.05). Conclusions: In accordance with other studies, we showed that HCV infection induces a dramatic increase in Tregs, which might contribute to the immune response failure during HCV infection.
https://iji.sums.ac.ir/article_17054_3fa6a00df422ef11d15ec6eeca3fef3c.pdf
2010-09-01
177
185
Hepatitis C Virus
Flowcytometry Method
Natural Regulatory T Cells
Tyebeha
Hashempoor
1
Department of Virology, School of Medical Sciences, Tarbiat Modares University of Medical Sciences
AUTHOR
Taravat
Bamdad
bamdad_t@modares.ac.ir
2
Department of Virology, School of Medical Sciences, Tarbiat Modares University of Medical Sciences
LEAD_AUTHOR
Shahin
Merat
3
Digestive Disease Research Center, Shariati Hospital, Tehran University of Medical Sciences
AUTHOR
Ehsan
Janzamin
4
Rooyan Institute
AUTHOR
Leila
Nemati
5
Rooyan Institute
AUTHOR
Hossain
Jabbari
6
Digestive Disease Research Center, Shariati Hospital, Tehran University of Medical Sciences
AUTHOR
Amir-Houshang
Sharifi
7
Digestive Disease Research Center, Shariati Hospital, Tehran University of Medical Sciences
AUTHOR
Hediyeh
Zamini
8
Digestive Disease Research Center, Shariati Hospital, Tehran University of Medical Sciences
AUTHOR
ORIGINAL_ARTICLE
Impact of Opium on the Serum Levels of TGF-β in Diabetic, Addicted and Addicted-Diabetic Rats
Background: Several cells of immune system such as regulatory T cells and macrophages secrete transforming growth factor-β (TGF-β) in response to different stimuli. This cytokine has inhibitory effect on immune system and diminished production of this cytokine is associated with autoimmune disorders. Objective: The aim of this study was to evaluate the influence of opium addiction on serum level of TGF-β in male and female diabetic and non-diabetic Wistar rats. Methods: This experimental study was performed on normal, opium addicted, diabetic and addicted-diabetic male and female rats. Serum level of TGF-β was measured by ELISA. Results: The results of our study indicated that the mean serum level of TGF-β in female addicted rats was significantly increased compared to control group (p<0.004). Conversely, in male addicted rats the mean serum level of TGF-β was lower compared with control (p<0.065). Conclusion: Our results suggest that opium and its derivatives have differential inductive effects on the cytokine expression in male and female rats.
https://iji.sums.ac.ir/article_17055_a30a7ba6e32a5214a80a718edb939bdc.pdf
2010-09-01
186
192
addiction
Diabetes
opium
TGF-β
Gholamreza
Asadikaram
asadi_ka@yahoo.com
1
Department of Clinical Biochemistry, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
LEAD_AUTHOR
Majid
Asiabanha
2
Department of Clinical Biochemistry, Qazvin University of Medical Sciences, Qazvin, Iran
AUTHOR
Ahmadreza
Sayadi
3
Departments of Psychology
AUTHOR
Abdollah
Jafarzadeh
jafarzadeh14@yahoo.com
4
Immunology
AUTHOR
Gholamhossein
Hassanshahi
ghassanshahi@gmail.com
5
Hematology, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
AUTHOR
ORIGINAL_ARTICLE
Association of Salivary sCD14 Concentration Levels with Early Childhood Caries
Background: Early childhood caries (ECC) is a severe type of dental caries affecting infants and pre-school children. Because of the infectious nature of the disease, the immunologic response by the host plays an essential role in its development. Objective: This study investigated the association between the presence of salivary sCD14 and ECC. Methods: This study was carried out on 40 healthy children, of whom 20 were caries-free (CF) and 20 had ECC, within the ages of 36 to 71 months. Unstimulated saliva of the children was collected with disposable needle-less syringe from buccal and labial vestibules. Seven children with ECC received complete treatments. Saliva was collected for a second time after 3 months from this group. The sCD14 levels in salivary samples were analyzed by ELISA method. Results: Mean concentrations of sCD14 in ECC and CF groups were 57.82 and 31.92 ng/ml respectively (p=0.008). After three months, the mean concentration of sCD14 among the treated children decreased to 11.38 ng/ml, which was significantly lower compared to that of ECC children before intervention (p<0.001), and also CF children (p<0.05). Conclusion: The increased levels of sCD14 can be considered as a marker of inflammation and innate immune response during ECC.
https://iji.sums.ac.ir/article_17056_b94f13ba6fde2a20d733678244b97a9e.pdf
2010-09-01
193
197
dental caries
Saliva
sCD14
Mina
Biria
dr.biriam@gmail.com
1
Department of Pediatric Dentistry
LEAD_AUTHOR
Mandana
Sattari
mandana.sattari@gmail.com
2
Department of Immunology, Shahid Beheshti University of Medical Sciences,Tehran,Iran
AUTHOR
Mojtaba Vahid
Golpayegani
3
Department of Pediatric Dentistry
AUTHOR
Fahimeh
Kooshki
4
Department of Pediatric Dentistry, Ghazvin University of Medical Sciences, Ghazvin, Iran
AUTHOR
ORIGINAL_ARTICLE
Detection of Autoantibodies against Gangliosides in Guillain-Barré Syndrome
https://iji.sums.ac.ir/article_17057_94deaf503a8888c8f9ba407592abe62d.pdf
2010-09-01
198
201
Hong-Liang
Zhang
hongliang.zhang@ki.se
1
Department of Neurology, First Hospital of Jilin University, Changchun, China
LEAD_AUTHOR
Su-Jie
Gao
2
Department of Anaesthesia, China-Japan Union Hospital of Jilin University, Changchun, China
AUTHOR
Yi
Yang
3
Department of Neurology, First Hospital of Jilin University, Changchun, China
AUTHOR
Jiang
Wu
4
Department of Neurology, First Hospital of Jilin University, Changchun, China
AUTHOR
ORIGINAL_ARTICLE
Detection of Anti-Ganglioside Antibodies in Guillain-Barre Syndrome
https://iji.sums.ac.ir/article_17058_2a501ff19189b09c70ad1ca0ddbb7970.pdf
2010-09-01
198
201
Viroj
Wiwanitkit
wviroj@yahoo.com
1
Wiwanitkit House, Bangkhae, Bangkok, Thailand 10160
LEAD_AUTHOR