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The role of complement receptor positive and complement receptor negative B cells in the primary and secondary immune response to thymus independent type 2 and thymus dependent antigens.

T Lindsten, L J Yaffe, C B Thompson, G Guelde, A Berning, I Scher and J J Kenny
J Immunol May 1, 1985, 134 (5) 2853-2859;
T Lindsten
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L J Yaffe
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C B Thompson
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G Guelde
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A Berning
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I Scher
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J J Kenny
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Abstract

Both complement receptor positive (CR+) and complement receptor negative (CR-) B cells have been shown to be involved in the primary immune response to PC-Hy (phosphocholine conjugated hemocyanin), a thymus dependent (TD) antigen which preferentially induces antibody secretion in Lyb-5+ B cells during a primary adoptive transfer assay. CR+ and CR- B cells also responded in a primary adoptive transfer assay to TNP-Ficoll, a thymus independent type 2 (TI-2) antigen which activates only Lyb-5+ B cells. When the secondary immune response to PC-Hy and TNP-Ficoll were analyzed, it was found that most of the immune memory to both antigens was present in the CR- B cell subset. The CR- B cell subset also dominated the secondary immune response to PC-Hy in immune defective (CBA/N X DBA/2N)F1 male mice. These data indicate that CR- B cells dominate the memory response in both the Lyb-5+ and Lyb-5- B cell subsets of normal and xid immune defective mice and suggest that Lyb-5+ and Lyb-5- B cells can be subdivided into CR+ and CR- subsets.

  • Copyright © 1985 by American Association of Immunologists

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The Journal of Immunology
Vol. 134, Issue 5
1 May 1985
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The role of complement receptor positive and complement receptor negative B cells in the primary and secondary immune response to thymus independent type 2 and thymus dependent antigens.
T Lindsten, L J Yaffe, C B Thompson, G Guelde, A Berning, I Scher, J J Kenny
The Journal of Immunology May 1, 1985, 134 (5) 2853-2859;

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The role of complement receptor positive and complement receptor negative B cells in the primary and secondary immune response to thymus independent type 2 and thymus dependent antigens.
T Lindsten, L J Yaffe, C B Thompson, G Guelde, A Berning, I Scher, J J Kenny
The Journal of Immunology May 1, 1985, 134 (5) 2853-2859;
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Print ISSN 0022-1767        Online ISSN 1550-6606