eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
65
75
16890
مقاله پژوهشی
Strong Immune Responses Induced by a DNA Vaccine Containing HPV16 Truncated E7 C-terminal Linked to HSP70 Gene
Zahra Meshkat
1
Hoorieh Soleimanjahi
soleim_h@modares.ac.ir
2
Hessam Mirshahabi
3
Mojtaba Meshkat
4
Maryam Kheiandish
5
Zuhair Mohammad Hassan
6
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran
School of Medicine, Islamic Azad University, Mashhad
Blood Transfusion Center, Tehran, Iran
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran
Background: Vaccines capable of controlling tumor virus based infections are found difficult to develop due to the consistence latent infection in the host. DNA vaccines are attractive tools for the development of HPV vaccines and inducing antigen-specific immunity owing to the stability, simplicity of delivery, safety and cost effectiveness. However, there is a need to increase their potency by procedures such as using HSP70 gene as an adjuvant. Objective: To evaluate a DNA vaccine containing HPV16 truncated E7 C-terminal cytotoxic T-lymphocyte epitopes linked to HSP70 gene (HSP70-tE7) in an animal model. Methods: Mice were immunized with the plasmid DNA after pre-treatment with cardiotoxin. The splenocytes of immunized mice were then tested for CTL activity by detecting the apoptosis and necrosis in target cells, cytokine production by ELISA, CD4 and CD8 frequencies by flow cytometry, and lymphocyte stimulation by MTT assay. Results: The recombinant expression vector was able to elicit immune responses close to that of full length E7 complete gene. Although the use of a small part of a target antigen can induce immune responses equivalent to the full length antigen, it fails to elicit statistically significant stronger immune responses when fused with HSP70 compared to the complete E7 gene alone. Conclusion: The potent immunogenicity of HPV16 E7 was preserved in the HSP70-tE7 vaccine and may represent a target of choice for the therapeutic vaccination strategies. However, to improve the immunogenicity polytope DNA vaccines which elicit multiple effector and memory CTL responses should be considered in future studies of DNAbased cancer vaccines.
https://iji.sums.ac.ir/article_16890_acbfbe7e56fecf1675a2daf50ce8c835.pdf
CTL Epitope
DNA vaccine
E7
HSP70
Human papillomavirus type 16
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
76
84
16891
مقاله پژوهشی
Effect of LIGHT Adjuvant on Kinetics of T-Cell Responses Induced by HSV-1 DNA Immunization
Masumeh Gorgian Mahmoody
1
Taravat Bamdad
bamdad_t@modares.ac.ir
2
Maoud Pasania
3
Hoorieh Soleimanjahi
soleim_h@modares.ac.ir
4
Somayeh Pouyanfard
5
Hamidreza Hashemi
6
Mohammad Asghari-Jafarabadi
7
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University
Tehran Medical Unit, Islamic Azad University
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University
Department of Biostatistics, Tarbiat Modares University, Tehran, Iran
Background: Studies on efficacy of various vaccines that prevent or reduce the primary and recurrent HSV-1 infection have demonstrated the importance of cellular immunity for protection against the infection. We previously used DNA vaccination to induce cellular immunity against HSV-1 infection in mice. Objective: The aim of our study was to evaluate the effect of LIGHT, a member of TNF super family, on the kinetic of CTL response induced by HSV-1 glycoprotein B based DNA vaccine. Methods: Using a granzyme B ELISA for detection and analysis of CD8+ T cells, CTL activity was determined in the spleen of BALB/c mice at various time points after primary and booster dose of vaccination. The kinetics of CTL response to primary and secondary HSV-1 infection and DNA vaccination were compared to those induced by DNA vaccination in combination with LIGHT adjuvant in the present study. Results: In primary and secondary immunization, the CTL activity in the HSV injected group peaked 7 days and 12 hours post immunization, respectively. After 5 days, LIGHT could neither accelerate the CTL response compared to DNA vaccination alone nor could enhance the CTL activity in the primary and the first peak of memory response, the amount of granzyme B induced by the LIGHT containing vaccine was significantly higher than that induced by the vaccine without the adjuvant. Conclusion: Although LIGHT enhances the cellular response in the booster dose of vaccination, it does not accelerate the CTL response.
https://iji.sums.ac.ir/article_16891_faac039dc5dff0ed79fbc8ce7c018b98.pdf
Activity
Cytotoxic T-Lymphocytes
HSV-1
infection
Light
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
85
89
16892
مقاله پژوهشی
HLA-B27 Association with Uveitis in an Asian Indian Population
Mahendra Narin Mishra
1
Khurshed Minoo Bharucha
2
Dr. Lal Pathology Reference Laboratory, New Delhi
Department of Ophthalmology, Command Hospital (SC), Pune, India
Background: Uveitis refers to diseases characterized by intraocular inflammation of the uveal tract. Anterior uveitis is a common ocular disease characterized by inflammation of the iris and the ciliary body. Objectives: To establish the frequency of HLA-B27- positive uveitis in Asian Indian population, study their clinical profile and compare it with other reports in literature. Methods: We retrospectively reviewed medical data of 89 patients of uveitis referred for HLA B27 typing with predominantly ocular symptoms during the period from April 2006-October 2010. All patients were tested for complete blood count, erythrocyte sedimentation rate, infectious diseases serology, HLA-B27 typing, and prepared radiographs of the sacroiliac joints and lumbar spine if required. Results: The HLA-B27 positive rate was 56.2% among patients and 3% for control samples. Most of the patients were in the age group of 41-50 years with a male predominance. Conclusions: HLA-B27 was seen to be associated with acute anterior uveitis in Asian Indian males and the test is important for confirmation of diagnosis, prognostication and also for planning the treatment.
https://iji.sums.ac.ir/article_16892_402f5d2aabd8b7454477f8159398f64d.pdf
Asian
HLA-B27
Indian
Uveitis
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
90
95
16893
مقاله پژوهشی
Stromal Cell Derived Factor-1 Genetic Variation at Locus 801 in Patients with Myasthenia Gravis
Gholam ALi Yousefipour
1
Mohammad Reza Haghshenas
2
Sara Yahyazadeh
3
Nasrollah Erfani
erfanin@sums.ac.ir
4
Department of Neurology
Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran
Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran
Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran
Background: Myasthenia gravis (MG) is the most common disorder of neuromuscular junction in which autoantibodies develop against nicotinic acetylcholine receptor for unknown reasons. The association of immunomodulator genes with different autoimmune disease has been studied in recent years. Objective: The aim of this study was to investigate correlation between a genetic variation in Stromal Cell Derived Factor-1 (SDF1) and susceptibility to MG in an Iranian population. Methods: Genotyping of SDF1 at position 801 G/A was performed by Polymerase Chain Reaction-Restriction Length Polymorphism (PCR-RFLP) in 87 patients with confirmed myasthenia gravis and 261 normal control subjects. Results: No statistically significant differences were observed in the frequencies of genotypes and alleles between patients and controls (p>0.05). Furthermore, no significant differences in the genotype distribution were found between the cases with different stages (p>0.05). Conclusion: Our data suggest that the SDF1 gene polymorphism at position 801 G/A is not associated with myasthenia gravis
https://iji.sums.ac.ir/article_16893_b0d01c7f5f110b22f94f40b7be8d618c.pdf
Polymorphism
Myasthenia gravis
SDF1
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
96
103
16894
مقاله پژوهشی
Immunomodulatory Activity of the Aqueous Extract of Seeds of Abrus precatorius Linn (Jequirity) in Mice
Anita Tilwari
anita_tilwari@yahoo.com
1
Narmada Prasad Shukla
2
Uma Devi Pathirissery
3
Centre of Excellence in Biotechnology, Madhya Pradesh Council of Science and Technology
School of Biotechnology, Rajiv Gandhi Proudyogiki Vishwavidyalaya (State Technological University)
Jawahar lal Nehru Cancer Hospital and Research Centre, Bhopal, Madhya Pradesh, India
Background: Various compounds of plant origin have been widely investigated since ancient times for their possible immunomodulatory properties as well as for the treatment of a wide range of diseases. Objective: To study the immunomodulatory functions of the aqueous extract of the seeds of Abrus precatorius commonly known as Indian liquorice (Fabaceae), a medicinal plant native to central India. Methods: Swiss albino mice were intraperitoneally treated with three doses (0.75, 1.25 and 2.5 μg/kg b.w.) of extract for 7 days. Relative organ weight, delayed type hypersensitivity (DTH) response, haemagglutination titre (HT) and Phagocytic index (PI) were studied in various groups of animals. Results: The results showed no significant difference in relative organ weight of spleen, liver, thymus and kidney in various groups of animals. Treatment of rats with increasing concentrations of the extract decreased the footpad thickness indicating a dose related inhibitory effect of the extract on delayed type hypersensitivity. In the HT test, the plant extract showed a suppressive effect at all doses, and these changes were significant as the dose increased. Phagocytic index was also increased in a dose dependent manner. Conclusion: The reduction of antibody titre, delayed type hypersensitivity response and the increase in phagocytic index indicates that Abrus precatorius has an inhibitory effect on the immune functions in mice.
https://iji.sums.ac.ir/article_16894_b79b8d1de157cabc79bfe0f3a4d3ad8d.pdf
Abrus precatorius
Delayed Type Hypersensitivity
Haemagglutination
Immunomodulation
Phagocytic Index
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
104
110
16895
مقاله پژوهشی
Clinical, Histopathological and Immunofluorescent Findings of IgA Nephropathy
Hamid Nawaz Tipu
1
Tahir Aziz Ahmed
2
Muhammad Mokarram Bashir
3
Combined Military Hospital, Chunian Cantt
Department of Immunology, Armed Forces Institute of Pathology, Rawalpindi, Pakistan
Department of Immunology, Armed Forces Institute of Pathology, Rawalpindi, Pakistan
Background: IgA nephropathy, a prevalent disease in Asia, is considered the main cause of end stage renal disease among primary glomerular disease. Objective: To determine the frequency of different clinical, histopathological and immunofluorescent characteristics of IgA nephropathy. Methods: Renal biopsies of 376 patients were received for immunofluorescent and for histopathological studies. Biopsies were stained with fluorescene isothyocyanate (FITC) labeled antibodies against IgG, IgA, IgM, C3, C4 and fibrinogen for fluorescent microscopy. For histopathological examination, the specimens were stained with hematoxylin and eosin, periodic acid schiff and methanamine silver stains for light microscopy. Results: IgA nephropathy was diagnosed in 39 cases (10.4%) with a mean age 31.5 years and a male to female ratio of 2.8:1. The disease was observed in 11(29.7%) patients aged 21-30 years, followed by 8 patients (21.6%) aged 11-20 years group. Nephrotic range proteinuria was the most common laboratory finding which was detected in 11 patients (37%). Mesangioproliferative glomerulonephritis was the most common histopathological finding which was found in 7 patients (35%). IgA with other immunoglobulins and complements were deposited in 28 specimens (71.8%) as detected by immunofluorescence. Conclusion: IgA nephropathy is common in young people and one third of it results in end stage renal disease. We suggest that Immunofluorescent assay can be considered for the conclusive diagnosis of IgA nephropathy in young patients presenting with proteinuria/hematuria.
https://iji.sums.ac.ir/article_16895_a0c3d28c65c333487e4440da696b7ddd.pdf
Glomerulonephritis
IgA Nephropathy
Immunofluorescence
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
111
119
16896
مقاله پژوهشی
Down-Regulation of CD14 Transcripts in Human Glioblastoma Cell Line U87 MG
Alireza Haghparast
alireza.haghparast@gmail.com
1
Maryam Heidari Kharaji
2
Amir Mohammad Malvandi
3
Laboratory of Immunoregulation, Department of Pathobiology, Faculty of Veterinary Medicine
Laboratory of Immunoregulation, Department of Pathobiology, Faculty of Veterinary Medicine
Laboratory of Immunoregulation, Department of Pathobiology, Faculty of Veterinary Medicine
Background: Pattern recognition receptors (PRRs) are the main sensors of pathogen and danger signals in innate immunity of which Toll Like Receptors (TLRs) are the most studied ones. The contribution of PRRs in cerebral inflammation induced by microbial infection, tissue damage and cancer has not extensively been addressed so far. Glioma is the most common tumor of the central nervous system and glioblastomas are the most common and most malignant primary brain tumors. Objective: The objectives of the present study were to investigate the expression of several PRRs including TLR2, TLR4, MyD88 and CD14 transcripts in human glioblastoma cell line U87 MG and compare their expression level with peripheral blood mononuclear cells (PBMC) obtained from healthy individuals. Methods: Touchdown PCR (TD-PCR) and Realtime quantitative PCR (qPCR) were applied to detect and quantify the expression level of TLR2, TLR4, MyD88 and CD14 transcript in U87 MG cell line and (PBMC) of healthy individuals. Results: According to our results, human glioblastoma cell line U87 MG expresses TLR2, TLR4, MyD88 and CD14 transcripts in TD-PCR. Moreover, the quantification of the expression of these genes revealed a highly significant downregulation of CD14 and a slight up-regulation of TLR2 transcripts as compared to PBMC of healthy individuals. Conclusion: The lower expression level of CD14 in human glioblastoma cell line, might have a potential implication for CD14 mediated cerebral pathology.
https://iji.sums.ac.ir/article_16896_250bd9a505ac3c3addf21a7b4db6acff.pdf
CD14
Cell Line
Glioblastoma
Toll-Like Receptor
eng
Shiraz Institute for Cancer Research
Iranian Journal of Immunology
1735-1383
1735-367X
2011-06-01
8
2
120
126
16897
مقاله پژوهشی
Profiles of MMP-2 Expression in Jurkat, Molt-4 and U937 Cells
Fatemeh Hajighasemi
1
Department of Immunology, Faculty of Medicine, Shahed University, Tehran, Iran
Background: Leukemia is a malignant proliferative disorder of the hematopoietic cells. The important role of angiogenesis in leukemia has been reported by several studies. Matrix metalloproteinases (MMPs) are a large group of endopeptidases which degredate the extracellular matrix and play an important role in angiogenesis. Objective: The present study was conducted to evaluate the patterns of MMP-2 activity in three leukemic cell lines. Methods: Human leukemic monocyte (U937) and T cells (Molt-4 and Jurkat) were cultured in complete RPMI-1640 medium. The cells were then seeded at a density of 106 cells/ml and were incubated with different concentrations of phorbol myristate acetate (PMA) (1-25 ng/ml) or phytoheamagglutinin (PHA) (2-10 μg/ml) for 24 hours. The MMP-2 activity in cell-conditioned media was then evaluated by gelatin zymography. Statistical comparisons between groups were made by analysis of variance (ANOVA). Results: PHA/PMA significantly and dose-dependently increased MMP-2 activity in U937 cells after 24 hours of incubation compared with untreated control cells. Moreover, PHA/PMA significantly induced MMP-2 activity in Molt-4 and Jurkat cells after 24 hours of incubation in a dose-dependent manner compared with untreated control cells. Conclusion: We conclude that human leukemic Jurkat, U937 and Molt-4 cells could potentially display MMP-2 activity with different degrees. Thus, these cell lines could provide an appropriate system to study the mechanisms regulating MMPs production in leukemia patients.
https://iji.sums.ac.ir/article_16897_b317a8a6fc7b4b9e6702c9cc197debe8.pdf
Cell Line
Leukemia
MMP-2