Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
1984-10-19
pubmed:abstractText
The splenic component of reticulophagocytic function (RPF) was examined in 29 insulin-treated diabetic subjects (13 type I and 16 type II) by measurement of clearance of altered, radiolabeled, autologous erythrocytes. Double-isotope studies were performed with cells altered by: (1) preincubation with N-ethylmaleimide (NEM) and (2) coating with IgG antibody to the Rhesus (Rh) D antigen, labeled with 99mTc and 51Cr, respectively. HLA typing for the A, B, and DR loci was performed in those patients showing a defect in the clearance of IgG-coated cells. Values for half-life (t1/2) were correlated with the incidence of diabetic complications, levels of HbA1, and circulating immune complexes (CIC). Two patterns of abnormal clearance were observed: first, an isolated defect of IgG-coated cell clearance in 7 patients (3 had the HLA B8/DR3 haplotype) and second, abnormal removal of both types of cell in a further 7 patients (3 had B8/DR3). There was no correlation between half-lives as measured by the two methods, although exclusion of the patients with a defect of IgG-coated cell clearance alone yielded a highly significant correlation for the remaining 15 Rh-positive patients (P less than 0.01). Abnormalities of IgG-coated cell clearance were more frequent in patients with HbA1 greater than 9% (P less than 0.02), while t1/2 of NEM-altered cells was significantly greater in patients with CIC (P less than 0.05). There was no correlation between t1/2 and the incidence of peripheral complications.(ABSTRACT TRUNCATED AT 250 WORDS)
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0012-1797
pubmed:author
pubmed:issnType
Print
pubmed:volume
33
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
813-8
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:6381177-Adolescent, pubmed-meshheading:6381177-Adult, pubmed-meshheading:6381177-Aged, pubmed-meshheading:6381177-Animals, pubmed-meshheading:6381177-Antigen-Antibody Complex, pubmed-meshheading:6381177-Chromium Radioisotopes, pubmed-meshheading:6381177-Complement System Proteins, pubmed-meshheading:6381177-Diabetes Mellitus, pubmed-meshheading:6381177-Diabetes Mellitus, Type 1, pubmed-meshheading:6381177-Diabetes Mellitus, Type 2, pubmed-meshheading:6381177-Diabetic Nephropathies, pubmed-meshheading:6381177-Diabetic Retinopathy, pubmed-meshheading:6381177-Erythrocytes, pubmed-meshheading:6381177-Female, pubmed-meshheading:6381177-HLA Antigens, pubmed-meshheading:6381177-Half-Life, pubmed-meshheading:6381177-Humans, pubmed-meshheading:6381177-Immunoglobulin G, pubmed-meshheading:6381177-Insulin, pubmed-meshheading:6381177-Macrophages, pubmed-meshheading:6381177-Male, pubmed-meshheading:6381177-Middle Aged, pubmed-meshheading:6381177-Rabbits, pubmed-meshheading:6381177-Reticulocytes, pubmed-meshheading:6381177-Spleen, pubmed-meshheading:6381177-Technetium
pubmed:year
1984
pubmed:articleTitle
Factors influencing reticulophagocytic function in insulin-treated diabetes.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't