جستجوی مقالات مرتبط با کلیدواژه "antigenemia" در نشریات گروه "پزشکی"
جستجوی antigenemia در مقالات مجلات علمی
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Rotaviruses (RVs), a member of Reoviridae family, are a major cause of severe diarrhea in children < 5 years of age worldwide, infecting mainly the gastrointestinal tract although recent findings have shown extraintestinal spread of RV infections. The RV is known to cause systemic infection in children with acute gastroenteritis (AGE). The systemic RV infection may lead to the virus reaching extraintestinal organs, therefore developing clinical symptoms. RV RNA, antigen, and infectious particles have been found in serum, cerebrospinal fluid (CSF) and extraintestinal tissues in children with acute gastroenteritis (AGE). According to previous studies on molecular genotyping of RV, no specific association has been yet found between antigenemia and RV G genotype. However, nucleotide changes and genotype discordance in RVs have been detected in paired stool and serum samples. In children, who show the evidence of antigenemia, RV genome is detectable in extraintestinal organs. Although, clinical significance of the laboratory findings remains to be determined.Keywords: Antigenemia, extraintestinal sites, rotavirus, viremia
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BackgroundToxoplasma gondii, the obligate intracellular parasite is life threatening in AIDS patients. Diagnosis of toxoplasmosis is based on serological methods especially increasing of IgM and IgG titers, but finding of parasite or its components (antigenemia) may be beneficial method in order to detection of acute toxoplasmosis in immunocompromised patients.MethodsNinety-four serum samples from HIV positive patients were collected from Sanandaj, Kordistan west of Iran. These patients were lived in Sanandaj of whom 26 were prisoners infected with HIV virus in prison. Toxoplasma gondii antibodies were determined by IgG ELISA. T. gondii antigen was identified by capture-ELISA. PCR was performed on samples with T. gondii antigenemia. CD4+ T cells counts had been determined by flowcytometry and were obtained from records of each patient.ResultsAmong the examined HIV seropositive individuals, 19.1% (18/94) and 5.3% (5/94) were positive for Toxoplasma-IgG and antigenemia, respectively. Besides, one of the samples was positively detected by PCR method. Mean age of participants was 37.9 ± 9.5 year. Prevalence of IgG antibody and antgenemia was higher in age group of 40-50 years old. The Mean of CD4+ T cells counts of participants (total of HIV+ patients, IgG positive patients and patients with antigenemia) was 699.2 ± 345.2, 655.1 ± 237.9 and 620.2 ± 215.1 respectively.ConclusionCapture-ELISA and PCR could confirm the T. gondii acute infection in HIV positive patients. For precise diagnosis of acute toxoplasmosis in HIV positive patient, performance of more studies based on more sensitive types of PCR is suggested.Keywords: Toxoplasma gondii, IgG ELISA, Capture, ELISA, PCR, Antigenemia
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International Journal of Women’s Health and Reproduction Sciences, Volume:2 Issue: 2, Winter 2014, PP 90 -93ObjectivesToxoplasma gondii is an obligate intracellular parasite that infects a broad range of warm- blooded animals including human. Tachyzoites of T.gondii invade the host cell, replicate and finally lead to the lysis of the cell. T. gondii is associated with congenital infection and it can cause encephalitis, or systemic infection in immunocompromised patients. It is important to know whether the infection is recently acquired or is chronic. Differentiation between acute and chronic infection has a dramatic impact, especially for the developing fetus. In this study, Toxoplasma gondii was detected in acute phase of infection in serum sample of a person who had been accidentally infected with tachyzoites of RH strain in the laboratory.Materials And MethodsAnti- T.gondii IgG antibody was prepared by rabbit immunization with soluble antigen of tachyzoites of RH strain. Capture- ELISA, immunoblotting and PCR were performed in the laboratory.ResultsAntigenemia and parasitemia was detected in serum sample of infected person by capture_ELISA, immunoblotting and PCR techniques respectively.ConclusionAcute T.gondii infection could be detectable in a short period of time in the sera of infected person.Keywords: Antigenemia, PCR, Toxoplasma
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هدفویروس سیتومگال انسانی بیماری زای اصلی ای است که سلامت بیماران دریافت کننده پیوند سلول های بنیادی خون ساز را تهدید می کند. برای تشخیص و پایش عفونت ویروس سیتومگال انسانی در دریافت کنندگان پیوند از روش های به خصوصی استفاده می شود. پژوهش حاضر با هدف بررسی کارایی روش های آنتی ژنمی pp65 و PCR کیفی در پایش ویروس سیتومگال در این بیماران انجام شد.
مواد و روش هاتعداد 179 نمونه بالینی از 41 بیمار بررسی شد. در این مطالعه از یک PCR کیفی خانگی معتبر شده و از یک روش آنتی ژنمی تجاری استفاده شد. در نهایت نتایج به دست آمده به وسیله یک روش Real-time PCR کمی به عنوان استاندارد طلایی ارزیابی شد.
نتایجعفونت ویروس سیتومگال انسانی در 8/26 درصد و 6/42 درصد از بیماران به ترتیب بر اساس روش های آنتی ژنمی و PCR کیفی مشاهده شد. از مجموع 179 نمونه بالینی، 8/50 درصد به وسیله هر دو روش منفی بود و 2/21 درصد به وسیله هر دو روش مثبت شد. از سوی دیگر؛ 3/26 درصد نمونه ها منحصرا به وسیله PCR کیفی نتیجه مثبت را نشان داد و 7/1 درصد تنها به وسیله روش آنتی ژنمی، مثبت شد. مقایسه نتایج به دست آمده با روش Real-time PCR نشان داد که روش PCR کیفی دارای حساسیت بیشتری نسبت به روش آنتی ژنمی است (7/98 درصد در مقابل 7/45درصد). با این وجود ویژگی هر دو روش با هم برابر بود (8/96 درصد). به علاوه نتایج کمی حاصل از روش آنتی ژنمی دارای همبستگی مناسبی با روش Real-time PCR است (0001/0 >P 715/0R=).
نتیجه گیریهر دو روش آنتی ژنمی و PCR کیفی دارای نقایصی خاصی در تشخیص موثر عفونت ویروس سیتومگال انسانی است. از این رو به نظر می رسد مدیریت مناسب عفونت ویروس سیتومگال انسانی در بیماران پیوندی نیازمند روش های حساس کمی دیگری همچون qPCR است.
کلید واژگان: آنتی ژنمی, ویروس سیتومگال, PCR, pp64, Real, time PCRObjectivesHuman cytomegalovirus (CMV) is a major life-threatening pathogen for hematopoietic stem cell transplant recipients. Specific tests are used for the diagnosis and monitoring of CMV infection in transplant patients. This study evaluates the performance of pp65 antigenemia and qualitative PCR assays for monitoring CMV in such patients.MethodsWe analyzed 179 clinical samples from 41 patients by using a validated home-brewed qualitative PCR and a commercial antigenemia assay. The obtained results were evaluated using quantitative real-time PCR as the gold standard.ResultsCMV was observed in 26.8% of samples analyzed by the antigenemia assay and in 42.6% of the samples by qualitative PCR. Among 179 clinical samples, 50.8% were negative and 21.2% were positive by both assays. On the other hand, 26.3% were only positive by qualitative PCR whereas 1.7% were positive by the antigenemia assay. A comparison of the results with real-time PCR showed that qualitative PCR has a higher sensitivity than the antigenemia assay (98.7% vs. 45.7%). The specificity of both assays was equal (96.8%). Quantitative results of the antigenemia assay showed good correlation with real-time PCR (r=0.715; p<0.001).ConclusionBoth the qualitative PCR and antigenemia assays have special deficiencies for efficient diagnosis of CMV infection. Therefore, effective management of CMV infection in transplant patients requires the use of other sensitive quantitative methods such as qPCR.Keywords: Antigenemia, Cytomegalovirus, PCR, pp65, Real, time PCR
نکته
- نتایج بر اساس تاریخ انتشار مرتب شدهاند.
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