High-throughput allogeneic antibody detection using protein microarrays. 2016

Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
Division of Blood and Marrow Transplantation, Stanford University School of Medicine, 269 West Campus Dr., CCSR #2205, Stanford, CA 94305, United States. Electronic address: jedpaul@stanford.edu.

Enzyme-linked immunosorbent assays (ELISAs) have traditionally been used to detect alloantibodies in patient plasma samples post hematopoietic cell transplantation (HCT); however, protein microarrays have the potential to be multiplexed, more sensitive, and higher throughput than ELISAs. Here, we describe the development of a novel and sensitive microarray method for detection of allogeneic antibodies against minor histocompatibility antigens encoded on the Y chromosome, called HY antigens. Six microarray surfaces were tested for their ability to bind recombinant protein and peptide HY antigens. Significant allogeneic immune responses were determined in male patients with female donors by considering normal male donor responses as baseline. HY microarray results were also compared with our previous ELISA results. Our overall goal was to maximize antibody detection for both recombinant protein and peptide epitopes. For detection of HY antigens, the Epoxy (Schott) protein microarray surface was both most sensitive and reliable and has become the standard surface in our microarray platform.

UI MeSH Term Description Entries
D007518 Isoantibodies Antibodies from an individual that react with ISOANTIGENS of another individual of the same species. Alloantibodies
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011237 Predictive Value of Tests In screening and diagnostic tests, the probability that a person with a positive test is a true positive (i.e., has the disease), is referred to as the predictive value of a positive test; whereas, the predictive value of a negative test is the probability that the person with a negative test does not have the disease. Predictive value is related to the sensitivity and specificity of the test. Negative Predictive Value,Positive Predictive Value,Predictive Value Of Test,Predictive Values Of Tests,Negative Predictive Values,Positive Predictive Values,Predictive Value, Negative,Predictive Value, Positive
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002908 Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). Chronic Condition,Chronic Illness,Chronically Ill,Chronic Conditions,Chronic Diseases,Chronic Illnesses,Condition, Chronic,Disease, Chronic,Illness, Chronic
D004797 Enzyme-Linked Immunosorbent Assay An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed. ELISA,Assay, Enzyme-Linked Immunosorbent,Assays, Enzyme-Linked Immunosorbent,Enzyme Linked Immunosorbent Assay,Enzyme-Linked Immunosorbent Assays,Immunosorbent Assay, Enzyme-Linked,Immunosorbent Assays, Enzyme-Linked
D005260 Female Females
D006086 Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. Graft-Versus-Host Disease,Homologous Wasting Disease,Runt Disease,Graft-vs-Host Disease,Disease, Graft-Versus-Host,Disease, Graft-vs-Host,Disease, Homologous Wasting,Disease, Runt,Diseases, Graft-Versus-Host,Diseases, Graft-vs-Host,Graft Versus Host Disease,Graft-Versus-Host Diseases,Graft-vs-Host Diseases
D006182 H-Y Antigen A sex-specific cell surface antigen produced by the sex-determining gene of the Y chromosome in mammals. It causes syngeneic grafts from males to females to be rejected and interacts with somatic elements of the embryologic undifferentiated gonad to produce testicular organogenesis. HY Antigen,GA-1 Germ Cell Antigen,Antigen, H-Y,Antigen, HY,GA 1 Germ Cell Antigen,H Y Antigen

Related Publications

Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
October 2004, Expert review of proteomics,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
September 2007, Expert review of molecular diagnostics,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
November 2001, Genome research,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
January 2009, Methods in molecular biology (Clifton, N.J.),
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
April 2010, Nature protocols,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
January 2010, Cancer biomarkers : section A of Disease markers,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
May 2013, Journal of proteome research,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
August 2007, Expert review of proteomics,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
April 2002, Human mutation,
Jed Paul, and Bita Sahaf, and Spenser Perloff, and Kelsi Schoenrock, and Fang Wu, and Hideki Nakasone, and John Coller, and David Miklos
April 2009, Expert review of proteomics,
Copied contents to your clipboard!