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Regulation of Antibody Response in Vitro

VI. Carrier-Specific Helper Cells for IgG and IgE Antibody Response¹

From the Department of Medicine of The Johns Hopkins University, School of Medicine at The Good Samaritan Hospital, Baltimore, Maryland 21239

Abstract

Rabbits were primed with DNP-coupled Ascaris antigen (DNP-Asc) precipitated with aluminum hydroxide gel, received a supplemental immunization with bovine globulin (BGG) or ragweed Fr. D (Rag), and their mesenteric lymph node cells were stimulated in vitro with DNP-Asc or DNP-secondary carrier conjugate (DNP-BGG or DNP-Rag). IgM, IgG, and IgE antibodies were all formed in vitro, when the cells were stimulated with DNP-Asc. Stimulation of the same cells with DNP-secondary carrier also resulted in the formation of anti-DNP-antibodies of the three immunoglobulin classes, when donors of lymphocytes received the carrier with alum. Carrier-specific cells generated by the supplemental immunization with the same carrier in complete Freund's adjuvant (CFA) showed helper function for IgM and IgG antibody response but not for IgE antibody response. Similarly, lymph node cells from the rabbits primed with DNP-Rag and receiving supplemental immunization with Asc in alum responded to DNP-Asc to form IgM, IgG and IgE antibodies. In this system, supplemental immunization with CFA was occasionally effective for IgE antibody response to DNP-Asc, however, alum was a more effective adjuvant than CFA to prepare a carrier-specific cell population having helper function for IgE antibody response. The helper function of the carrier specific cell population for IgE antibody formation did not have any relationship with either the helper function of the same cell population for IgG antibody response or with the size of the carrier-specific cell population estimated by ³H-thymidine uptake. Evidence was obtained that lack of IgE antibody response to DNP-secondary carrier with the lymphocytes from the CFA group was not due to an increase of precursors of carrier-specific antibody-forming B cells. The results indicated that carrier-specific helper cells for the IgE antibody response were different from those for IgG/IgM antibody response.

Footnotes

¹ This work was supported by Research Grants GB-27682 from National Science Foundation, a grant from John A. Hartford Foundation and partly by United States Public Health Service Grant AI-11202. This is publication No. 84 from The O'Neill Laboratories at The Good Samaritan Hospital.

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