Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2007-4-27
pubmed:abstractText
Renal transplant rejection and graft versus host reactions between HLA genetically-identical sibling (HLAgi) donor/recipient (D/R) pairs are thought to result from minor histocompatibility antigen (mHAg) disparities. We have compared two methods of measuring HLAgi D/R T lymphocyte responses to "matured" dendritic cells: 1.) a modified Cylex assay of CD4(+) ATP levels (MLDC-ATP) versus 2.) (3)H-thymidine uptake (MLDC-(3)H). The MLDC-ATP kinetics peaked at 48 hours versus the MLDC-(3)H at 7 days, and appeared more sensitive. We tested HLAgi (normal) volunteer siblings (NLs), and D/R sibling pairs before and after renal transplantation (pre-Tx and post-Tx). The overall frequencies of positive responses in the MLDC-ATP for HLAgi NLs, pre-Tx, and post-Tx D/R pairs were 63%, 50%, and 42%, respectively. The percentage with reciprocal responses was 37.5%, 20%, and 22.22%, respectively. In one set of three HLAgi (NLs) siblings (two males and one female), there was a nongender-associated differential response. There was no MLDC correlation with class I MHC-associated mHAg (SSP) incompatibility, nor could some MLDC positive reactive pairs theoretically process the necessary HLA-class I restriction molecules for presentation of known (nanomeric) mHAg peptides. Speculatively, the MLDC reflects class II MHC-restricted mHAg reactions (not yet definable), with possible effects of other polymorphic (nonhistocompatibility) immune response genes, and thereby may be a useful measurement of CD4(+) T-cell HLAgi transplantation immunity.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0198-8859
pubmed:author
pubmed:issnType
Print
pubmed:volume
68
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
350-61
pubmed:meshHeading
pubmed-meshheading:17462502-Adenosine Triphosphate, pubmed-meshheading:17462502-Autoantigens, pubmed-meshheading:17462502-CD4-Positive T-Lymphocytes, pubmed-meshheading:17462502-Dendritic Cells, pubmed-meshheading:17462502-Female, pubmed-meshheading:17462502-HLA Antigens, pubmed-meshheading:17462502-Histocompatibility, pubmed-meshheading:17462502-Histocompatibility Antigens Class II, pubmed-meshheading:17462502-Histocompatibility Testing, pubmed-meshheading:17462502-Humans, pubmed-meshheading:17462502-Kidney Transplantation, pubmed-meshheading:17462502-Lymphocyte Culture Test, Mixed, pubmed-meshheading:17462502-Male, pubmed-meshheading:17462502-Minor Histocompatibility Antigens, pubmed-meshheading:17462502-Polymorphism, Genetic, pubmed-meshheading:17462502-Sex Factors, pubmed-meshheading:17462502-Siblings, pubmed-meshheading:17462502-Thymidine, pubmed-meshheading:17462502-Transplantation Immunology
pubmed:year
2007
pubmed:articleTitle
A novel approach to detect donor/recipent immune responses between HLA-identical pairs.
pubmed:affiliation
Lillian Jean Kaplan Renal Transplant Center of the Division of Transplantation of the Department of Surgery, University of Miami, Leonard M. Miller School of Medicine, Miami, Florida 33101, USA. YJin@med.miami.edu
pubmed:publicationType
Journal Article