Differences in Antigenic Specificity of Human Normal Adult, Fetal, and Sickle Cell Anemia Hemoglobin

ثبت نشده
چکیده

By MORRIS GOODMAN, PH.D.* AND DAN H. CAMPBELL, Pn.D. T HE DEMONSTRATION by Pauling et al.’ that sickle cell anemia hemoglobin has a slightly higher isoelectric point (0.2 pH unit) than normal human adult hemoglobin and the reports of differences in ability to form nematic liquid crystals2 and solubility differences in strong salt solutions3 suggest that differences might also exist in immunochemical properties. Differences between antigenic specificity of fetal and normal adult hemoglobin have been reported by Darrow et al.4 Vecchio and Barbagello5 confirmed these findings and also concluded that sickle cell anemia hemoglobin had the same specificity as normal adult hemoglobin. Unfortunately these two studies were carried out by means of the precipitin ring test so that it seemed desirable to repeat the study using more quantitative methods. Two sets of experiments were undertaken. The first, rather preliminary results indicated that normal adult and sickle cell anemia hemoglobin differ in their serologic behavior but that this could be explained on the basis of differences in physicochemical properties rather than antigenic specificity. The second series

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Differences in antigenic specificity of human normal adult, fetal, and sickle cell anemia hemoglobin.

By MORRIS GOODMAN, PH.D.* AND DAN H. CAMPBELL, Pn.D. T HE DEMONSTRATION by Pauling et al.’ that sickle cell anemia hemoglobin has a slightly higher isoelectric point (0.2 pH unit) than normal human adult hemoglobin and the reports of differences in ability to form nematic liquid crystals2 and solubility differences in strong salt solutions3 suggest that differences might also exist in immunoche...

متن کامل

Side Effects of Hydroxyurea in Patients with Sickle Cell Anemia

Background: Hemoglobin S arises is the result of a point mutation (A-T) in the sixth codon on the -globin gene on chromosome 11 causing sickle cell anemia. The presence of fetal hemoglobin in infancy plays a relatively protective role for vaso-occlusive symptoms that are the major contributor for the morbidity and mortality among patients with sickle cell anemia. hydroxyurea, an s-phase-specif...

متن کامل

The Influence of Fetal Hemoglobin on Clinical and Hematological Variables of Children and Adolescents with Sickle Cell Anemia in Basra, Southern Iraq

Background: There are many parameters that modulate the severity of sickle cell anemia. Fetal hemoglobin (Hb F) is one of these major variables. However, its effect is clinically inconsistent. We conducted a descriptive study to assess the influence of Hb F on clinical events and hematological variables in patients with sickle cell anemia. Methods: 151 patients with sickle cell anemia with a st...

متن کامل

Beta-Globin Gene Cluster Haplotypes in Iranian Sickle Cell Patients: Relation to Some Hematologic

Background: Sickle cell anemia is relatively common in Khuzestan province located in Southwest Iran. The characteristics of sickle cell disease in Iran are apparently different from other regions some of these characteristics might be related to β-chain haplotypes. The purpose of this study was to determine the frequency of β-chain haplotypes in 50 patients with homozygous sickle cell anemia in...

متن کامل

Pattern of chronic lung lesions in adults with sickle cell disease in Lagos, Nigeria

Background: The vascular response to recurrent tissue hypoxia and reperfusion following red blood cell sickling causes acute chest syndrome and chronic lung disease. The purpose of this study was to determine the pattern of chronic lung lesions and possible risk factors in sickle cell patients in lagos, Nigeria.Methods: From July 2012 to April 2013, Pulmonary function test (PFT) and chest-x-ray...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2005