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Iranian Journal of Basic Medical Sciences، جلد ۱۰، شماره ۲، صفحات ۱۳۲-۱۳۸
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عنوان انگلیسی Quantification Analysis of Dot Blot Assays for Human Immunodeficiency Virus Type 1 and 2 Antibodies
چکیده انگلیسی مقاله Objective Dot Blot (DB) assay provides highly specific results, but usually not reliable for quantification of antibody production. The need for a more objective DB assay to provide a better definition of the immune status, against HIV antigens, promoted this study to be done to develop a quantitative DB assay. Material and Methods Dot blot (DB) strips for antibodies directed to human immunodeficiency virus (HIV) type 1 and 2 were analyzed by a video densitometer. This method was used to quantify the antibody response to different HIV proteins in infected patients. In order to increase reproducibility, reagents and protocols were accurately standardized and internal controls were added. In the first format, an internal control band consisting of Human IgG was added to each dot to minimize the effects of band intensity variation. In the second format, antibody concentrations were calculated from the ratio of the densities produced by test sera and by positive and negative standard sera. Results The sera under scrutiny were also examined by standard enzyme-linked immunosorbent assay (ELISA) and the obtained results were compared with those of the corresponding DB. A statistically significant positive correlation was found between the results obtained with the two methods, and this was especially evident when ELISA titers were compared to corrected DB values (p = 0.001). Conclusion Densitometric analysis of DB assays led to quantify the antibodies against HIV-1 and 2 Gag and Env proteins and might be useful to investigate possible humoral immune correlates of production in HIV vaccine studies and antibody production in the early phase of infection.
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نویسندگان مقاله m روانشاد | m. ravanshad
department of virology, faculty of medical sciences, tarbiat modarres university, tehran, iran

سازمان اصلی تایید شده: دانشگاه تربیت مدرس (Tarbiat modares university)

f صباحی | f. sabahi
department of virology, faculty of medical sciences, tarbiat modarres university, tehran, iran

سازمان اصلی تایید شده: دانشگاه تربیت مدرس (Tarbiat modares university)

f مهبودی | f. mahboudi
biotechnology research center, pasture institute of iran, tehran, iran
نشانی اینترنتی http://ijbms.mums.ac.ir/article_5280.html
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زبان مقاله منتشر شده en
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نوع مقاله منتشر شده Original Article
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