B cell stimulatory factor-1 enhances the IgE response of lipopolysaccharide-activated B cells.

Robert L. Coffman(Institut de Biologie Moléculaire et Cellulaire), J Ohara(National Institutes of Health), M W Bond(Institut de Biologie Moléculaire et Cellulaire), J E Carty(Institut de Biologie Moléculaire et Cellulaire), Albert Zlotnik(Institut de Biologie Moléculaire et Cellulaire), W E Paul(National Institutes of Health)
The Journal of Immunology
June 1, 1986
Cited by 797Open Access
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Abstract

Supernatants from some mouse helper T cell (TH) lines contain an activity that can enhance IgE production by lipopolysaccharide (LPS)-stimulated B cells by at least two orders of magnitude. During purification, this activity could not be resolved from B cell stimulatory factor-1 (BSF-1). Highly purified BSF-1 from a different source, the T lymphoma cell line EL-4, enhanced IgE production to the same extent as TH supernatants, which suggests that BSF-1 is responsible for this increase in IgE production. Monoclonal antibody to BSF-1 totally inhibits the IgE-enhancing activity of a TH supernatant, lending further support to this conclusion. The effects of BSF-1 on LPS-stimulated B cells are specific for IgE and, as previously reported, IgG1 and IgG3, because the levels of IgM, IgG2a, IgG2b, and IgA in the cultures change relatively little when BSF-1 is added.


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