Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1983;15(2):69-77.
doi: 10.1007/BF00199693.

A 125I-protein A-binding assay detecting antibodies to cell surface antigens. Evidence for the presence of specific antibodies against leukemia-associated antigens in human leukemias

Comparative Study

A 125I-protein A-binding assay detecting antibodies to cell surface antigens. Evidence for the presence of specific antibodies against leukemia-associated antigens in human leukemias

R Fäldt et al. Cancer Immunol Immunother. 1983.

Abstract

A 125I-protein A-binding assay detecting antibodies to cell surface antigens on human blood cells was developed and evaluated using sera from multitransfused nonleukemic patients sensitized against HLA antigens. The binding assay was found to be reproducible and more sensitive than conventional HLA testing. Seven patients with acute myelogenous leukemia and two patients with acute lymphoblastic leukemia successfully treated by chemotherapy were then investigated. Sera from seven of the patients studied in partial or complete remission demonstrated significant binding to autochthonous leukemic cells obtained from bone marrow or peripheral blood. In two cases sera taken during the leukemic stage demonstrated the most pronounced binding to the patients' own leukemic cells. Sera from four patients with demonstrable significant binding to autochthonous leukemic cells failed to bind to autochthonous remission cells when both types of target cells were tested in parallel. Differences in serum concentrations of IgG, IgA, and IgM were not the cause of the demonstrated increased binding of leukemic sera to autochthonous target cells. We propose that the 125I-protein A-binding assay presented in this paper detects antibodies reacting selectively with acute leukemia cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Baker MA, Falk JA, Taub RN. Immunotherapy of human acute leukemia: Antibody response to leukemia-associated antigens. Blood. 1978;52:469. - PubMed
    1. Baker MA, Mohanakumar T, Roncari DAK, Shumak KH, Falk JA, Aye MT, Taub RN. Leukemia markers. London: Academic Press; 1981. Human acute myeloblastic leukemia-associated antigens; p. 225.
    1. Bertini M, Galetto G, Comoglio PM. Immune complexes and circulating antibodies against autologous leukaemic cells in patients with acute leukemias. Immunology. 1982;45:569. - PMC - PubMed
    1. Biberfeld P, Ghetie V, Sjöquist J. Demonstration and assaying of IgG antibodies in tissues and on cells by labelled staphylococcal protein A. J Immunol Methods. 1975;6:249. - PubMed
    1. Billing R, Clark B, Koeffler P, Foon KA, Terasaki PI. Acute myelogenous leukemia heteroantisera. Clin Immunol Immunopathol. 1980;16:202. - PubMed

Publication types