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From The Department of Medicine, Johns Hopkins University School of Medicine at the Good Samaritan Hospital, Baltimore, Maryland 21239 and the Rockefeller University, New York, New York 10021
Abstract
Denaturation of antigen E in 8 M urea or by reduction-carboxymethylation treatment resulted in loss of antigenic determinants in native molecules. The denatured antigen preparations, as well as the
and
polypeptide chains isolated from the antigen upon its dissociation failed to combine with rabbit or human IgG antibody against the native antigen, or to induce erythema wheal reactions in ragweed-sensitive individuals. The denatured antigens and the polypeptide chains, however, enhanced anti-DNP antibody response of DNP-ragweed (DNP-Rag)-primed rabbit lymph node cells to DNP keyhole limpet hemocyanin (KLH). When the primed lymph node cells were treated with DNP-KLH for 24 hr, and then cultured in the presence of one of these modified antigens, both IgG and IgE anti-DNP antibodies were formed in vitro. The activity of the modified antigens to stimulate carrier-specific helper cells was comparable to that of native antigen. All of the modified antigens induced DNA synthesis of peripheral lymphocytes of ragweed-sensitive patients but not the lymphocytes of normal individuals. The results indicated that denatured antigen E as well as
and
polypeptide chains possess determinants specific for T cell receptor.
Footnotes
1 This work was supported by Research Grants AI-11202 and AI-08445 from United States Public Health Service. This is publication 119 from the O'Neill Laboratories at The Good Samaritan Hospital.
2 Awardee of International Fellowship IF-05TW01917 from United States Public Health Service. Present address: Department of Immunology, Hospital St. Pierre, Rue Haute, Bruxelles, Belgium 1006.
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