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High-throughput allogeneic antibody detection using protein microarrays.

Journal of immunological methods (2016-02-24)
Jed Paul, Bita Sahaf, Spenser Perloff, Kelsi Schoenrock, Fang Wu, Hideki Nakasone, John Coller, David Miklos
RESUMEN

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.

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Anti-Human IgG (Fc specific)-Cy3 antibody produced in goat, affinity isolated antibody, buffered aqueous solution