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1.
Pharmazie ; 57(8): 519-22, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12227189

ABSTRACT

The condensation of 1,5-diphenylpyrrolidine-2,4-dione (1) with the carboxyl compounds 2a-f afforded the corresponding 3-arylidene-1,5-diphenylpyrrolidine-2,4-diones 3a-f. Reaction of the parent compound 1 with isatin (4) yielded the condensation product 5 in an acidic medium, whereas compound 6 was obtained in an alkaline medium. The condensation of the primary amines 7a-f with compound 1 afforded the corresponding 4-substituted amino-1,5-diphenyl-delta 3-pyrrolin-2-ones 8a-f. All the compounds synthesized were screened for their antimicrobial activity, and four compounds were selected for screening for their antineoplastic activity. The compounds tested showed both antimicrobial and antineoplastic activities.


Subject(s)
Anti-Bacterial Agents/chemistry , Antineoplastic Agents/chemistry , Pyrrolidines/chemistry , Pyrrolidinones/chemistry , Anti-Bacterial Agents/chemical synthesis , Antineoplastic Agents/chemical synthesis , Bacteria/drug effects , Drug Screening Assays, Antitumor , Humans , Indicators and Reagents , Microbial Sensitivity Tests , Pyrrolidines/chemical synthesis , Quality Control , Spectrophotometry, Infrared , Tumor Cells, Cultured
2.
Eur J Epidemiol ; 15(7): 603-9, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10543349

ABSTRACT

A total of 202 serum and stool samples from acute hepatitis patients attending the Fever Hospital of Alexandria, Egypt, have been studied to reveal markers of hepatitis virus infection. Anti-HAV IgM were detected in 21 out of 202 sera (10.4%), whereas 201 sera (99.5%) had anti-HAV IgG. The first age attack was in the class-age 0-9 years with 64.7% of anti-HAV IgM positive sera. Among 202 patients, anti-hepatitis E IgG (sample/over cut off > 1.0) was identified in 90 patients (44.5%). The anti-HEV seropositivity ranged from 17.6% to 60.0% in the different age groups, with the highest level in the class-age 20 29 years. Anti-hepatitis E IgM were identified in 49 patients with the first age attack in the class-age 10-19 years (39.4%). HAV RNA was identified by nested PCR in 7 samples out of 15, whereas HEV RNA was present in 4 out of 75 stool samples. Direct DNA sequence of the latter PCR products confirmed the presence of the HEV genome; comparison of the sequences of the isolates from Egypt with those in data banks revealed the highest homology to the Burma strain. Our data confirm that HAV and HEV are common causes of acute sporadic hepatitis in Alexandria but with different peak age positivity. Occasionally, but not infrequently, dual infections (HAV-HEV and HEV-enteric viruses) were also found. The risk analysis indicates that patients living in rural areas are exposed to a higher risk of hepatitis E infection compared to the urban population, whereas the presence of anti-HEV IgG was significantly associated with consumption of common village water and use of indoor dry pit and oral therapy for schistosomiasis.


Subject(s)
Hepatitis A/diagnosis , Hepatitis A/epidemiology , Hepatitis E/diagnosis , Hepatitis E/epidemiology , Adolescent , Adult , Age Distribution , Aged , Base Sequence , Child , Child, Preschool , Comorbidity , Data Collection , Egypt/epidemiology , Feces/virology , Female , Hepatitis E virus/isolation & purification , Hepatovirus/isolation & purification , Hospitalization/statistics & numerical data , Humans , Incidence , Male , Middle Aged , Molecular Sequence Data , RNA, Viral/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction , Risk Factors , Seroepidemiologic Studies , Serologic Tests , Sex Distribution , Surveys and Questionnaires , Urban Population
3.
New Microbiol ; 22(2): 77-83, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10322605

ABSTRACT

Several human and animal cell lines have been used to grow hepatitis E virus. The strain SAR-55 was adapted only on PLF/PLC/5 cell line without any visible cytopathic effect. The growth of the SAR-55 was monitored by examining the positive and the negative strands of HEV-RNA. Stool samples, obtained from hospitalised acute hepatitis patients at the Fever Hospital of Alexandria (Egypt), were used to confirm the susceptibility of PLF/PLC/5 cells. After more than one-week's cultivation, three stool samples out of 17 IgM anti-HEV positive and 1 from 52 IgG anti-HEV positive patients showed a specific RT-PCR amplification product. The nucleotide sequences of the methyltransferase region of the genome in the isolates revealed the maximum homology with Burma strain with several point mutations.


Subject(s)
Hepatitis E virus/growth & development , Hepatitis E/virology , Animals , Base Sequence , Cell Line , DNA, Complementary , Feces/virology , Hepatitis E virus/genetics , Hepatitis E virus/isolation & purification , Humans , Methyltransferases/genetics , Molecular Sequence Data , RNA, Viral/analysis , Reverse Transcriptase Polymerase Chain Reaction/methods , Sequence Alignment , Sequence Analysis, DNA , Virus Cultivation , Virus Replication
4.
J Natl Cancer Inst ; 91(5): 465-9, 1999 Mar 03.
Article in English | MEDLINE | ID: mdl-10070947

ABSTRACT

BACKGROUND: In western countries, human herpesvirus-8 (HHV-8) appears to be transmitted mainly by sexual contact. To evaluate the role of other transmission routes, especially in developing countries, we estimated the seroprevalence of HHV-8 in Egyptian children, who, if seropositive, would have acquired the virus through a nonsexual route. METHODS: Sera from 196 children (<1-12 years of age), 20 adolescents (13-20 years of age), and 30 young adults (21-25 years of age) attending a vaccination program in Alexandria, Egypt, were studied. Immunofluorescence assays were used to detect antibodies against HHV-8 lytic-phase antigens (anti-lytic) and latent-phase antigens (anti-latent). Antibodies against Epstein-Barr virus viral cap antigen, cytomegalovirus, and HHV-6 were detected by enzyme-linked immunosorbent assays. Seroprevalence of these herpesviruses was calculated after stratifying the subjects by age. RESULTS: Anti-lytic and anti-latent HHV-8 antibodies were detected in 44.7% and 8.5% of the study participants, respectively. The prevalence of anti-lytic antibodies tended to increase with age, exceeding 50% in children older than 6 years; once children reached the age of 10 years, the prevalence tended to stabilize. The seroprevalence of other herpesviruses tended to be higher than that of HHV-8, ranging from approximately 83% to more than 97% in the 9- to 12-year age group. One- to 3-year-old children had higher titers of antilytic HHV-8 antibodies than children in the other age groups. Anti-latent antibodies were more frequently detected in individuals with high anti-lytic antibody titers. CONCLUSIONS: HHV-8 antibodies are highly prevalent in Egyptian children, suggesting that, in developing countries, HHV-8 infection may be acquired early in life through routes other than sexual transmission. The lower seroprevalence of HHV-8 relative to that of the other herpesviruses suggests that HHV-8 is less transmissible than other common herpesviruses.


Subject(s)
Antibodies, Viral/blood , Herpesviridae Infections/immunology , Herpesviridae Infections/transmission , Herpesvirus 8, Human/immunology , Adolescent , Adult , Child , Child, Preschool , Cytomegalovirus/immunology , Egypt/epidemiology , Enzyme-Linked Immunosorbent Assay , Female , Herpesvirus 4, Human/immunology , Herpesvirus 6, Human/immunology , Humans , Infant , Male , Seroepidemiologic Studies
5.
J Med Virol ; 53(4): 313-8, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9407377

ABSTRACT

The humoral immune response to HIV infection plays an important role in determining disease progression. Few and discordant results correlate changes in neutralizing antibody (NtAb) titer with antiretroviral treatment. The NtAb titer against autologous-HIV was evaluated in 33 patients treated with the protease inhibitor saquinavir (SQV, Invirase) and zidovudine (ZDV) alone or in combination. Ten out of 33 (30%) patients showed a significant increase (4-fold or greater) in NtAb titer from baseline in response to the initiation of therapy. A significant correlation (P = 0.007) was found between an increase in NtAb titer and treatment with SQV alone (5 subjects) or in combination (5 subjects). A significant decrease in NtAb titer was detected in 7 patients, 5 of whom were treated with ZDV alone. After one year of therapy a significant decrease in HIV-RNA copy number (> 0.5 log) with respect to baseline value was detected only in patients treated with SQV alone or in combination. Patients with increased NtAb titer showed a significantly reduced HIV-RNA copy number and increased CD4+ cell count at week 16 of treatment which were sustained up to week 52. These data suggest that treatment with SQV can improve neutralizing activity against autologous virus as well as bring about a significant and sustained reduction in viral load.


Subject(s)
Anti-HIV Agents/therapeutic use , HIV Antibodies/drug effects , HIV Infections/drug therapy , HIV-1/immunology , Saquinavir/therapeutic use , CD4 Lymphocyte Count/drug effects , Double-Blind Method , Drug Therapy, Combination , HIV Antibodies/blood , HIV Infections/immunology , HIV-1/genetics , Humans , Neutralization Tests , RNA, Viral/blood , RNA, Viral/drug effects , Time Factors , Viral Load , Zidovudine/therapeutic use
6.
Zentralbl Bakteriol ; 283(2): 239-44, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8825115

ABSTRACT

During the years 1992-1994, we tested 948 individuals from different population groups for HIV-1 and HIV-2 infections by ELISA and WB and for HCV infection by ELISA. Repeated ELISA reactivity for HIV was found in 2.12% of blood donors, 2.95% of fire brigade personnel and 1.61% of prisoners. Western blotting studies, however, showed that these samples were non-reactive or indeterminate to either HIV-1 or HIV-2. In contrast, anti-HCV antibodies were detected in 39% of fire brigade personnel, 31.4% of prisoners and 20.8% of blood donors. The analysis of risk factors for acquiring HCV infection showed a strong association between a past history of parenteral therapy for schistosomiasis and anti-HCV seropositivity (p < 0.0001). The implementation of preventive strategies is at the moment the mandatory choice to stop a further spread of the HCV infection. Meanwhile the same preventive measures could avoid spreading of the HIV disease.


Subject(s)
HIV Antibodies/blood , HIV Infections/epidemiology , Hepatitis C Antibodies/blood , Hepatitis C/epidemiology , Adult , Aged , Egypt , HIV Infections/immunology , HIV-1/immunology , HIV-2/immunology , Hepatitis B Antibodies/blood , Hepatitis B Surface Antigens/blood , Humans , Middle Aged , Pilot Projects , Prevalence , Risk Factors
7.
AIDS Res Hum Retroviruses ; 11(10): 1203-7, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8573376

ABSTRACT

Quantitative culture of human immunodeficiency virus (HIV) was performed on 202 plasma samples obtained from asymptomatic and early symptomatic HIV-1 infected patients (mean CD4+ count: 186/mm3) before antiretroviral therapy was started. HIV could be isolated from 84% of the plasma samples (titers ranging from 10(0) to 10(2.75) TCID50/ml). Immune complex dissociated p24 antigen (ICD-p24) was detected in 66% of the samples. Only 23 samples (11%) were negative for both ICD-p24 as well as HIV culture. Discordant results were obtained in 55 samples, and 45 samples negative for ICD-p24 were positive for HIV culture. A significant proportion (42%) of patients that were negative for ICD-p24 belonged to a very advanced group with very low CD4+ cell count. However, almost 90% of these ICD-p24 negative samples were positive for HIV plasma viremia, stressing the value of this virological marker in patients with low CD4+ cell count and without any detectable ICD-p24 antigenemia. HIV-1 RNA was detected in all ICD-p24 negative plasma samples tested by the branched DNA (bDNA) assay. A very good correlation was found between high RNA copy number and HIV plasma isolation in samples obtained from patients with low CD4+ cell count, suggesting that HIV-1 RNA quantitation may also reflect viral infectivity of plasma.


Subject(s)
HIV Core Protein p24/blood , HIV-1/isolation & purification , RNA, Viral/blood , Viremia/virology , Antigen-Antibody Complex/blood , Antigens, Viral/blood , CD4 Lymphocyte Count , HIV-1/genetics , Humans
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