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PMID: 2452184 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Picogram quantities of anti-Ig antibodies coupled to dextran induce B cell proliferation.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 140 ·No. 10 ·1988-05-15 ·Pages 3364-72

Brunswick M, Finkelman FD, Highet PF, Inman JK, Dintzis HM, Mond JJ

Abstract

To investigate the properties which enable type 2 Ag, as exemplified by dextran and Ficoll, to stimulate high levels of antibody responses in the relative absence of T cells, we conjugated anti-IgD and anti-IgM mAb to both dextran and Ficoll and examined their B cell-activating properties. Such conjugated anti-Ig antibodies stimulated both early and later stages of B cell activation at picogram concentrations, which are at least 1000-fold lower than that required for B cell stimulation by unconjugated anti-Ig antibodies, and the level of proliferation they stimulated was on average 10-fold greater. Furthermore, concentrations of anti-Ig dextran (100 pg/ml) which modulated little sIgD from the B cell surface were strong inducers of enhanced B cell expression of MHC class II molecules. Conjugation of Fab fragments of anti-IgD or nonmitogenic anti-IgM mAb to dextran rendered them as mitogenic as dextran conjugated to strongly stimulatory anti-IgD or anti-IgM antibodies. The ability of dextran and Ficoll to serve as effective carrier molecules for anti-IgD was not related solely to their large m.w., because anti-IgD coupled to polymerized BSA (m.w. 1.5 X 10(6), was only 10- to 50-fold more potent than unconjugated anti-IgD antibodies at stimulating B cell DNA synthesis. These results suggest, therefore, that the unique ability of picogram concentrations of haptenated type 2 Ag to stimulate Ig secretion in the absence of T cells may be a function of their ability to promote effective cross-linking without resulting in the modulation of sIg. This would enable such Ag to mediate repetitive B cell signaling, a situation that cannot be achieved by unconjugated anti-Ig antibodies which result in modulation of sIg at their mitogenic concentrations. These compounds therefore may be employed to study B cell activation stimulated by sIg cross-linking at concentrations that may more closely reflect those which are achieved under physiologic conditions by type 2 Ag.

MeSH Terms
Animals Antibodies, Anti-Idiotypic/analysis,physiology Antigens, Surface/analysis B-Lymphocytes/cytology,immunology Carrier Proteins/immunology,pharmacology Cross-Linking Reagents Dextrans/immunology,pharmacology Dose-Response Relationship, Immunologic Histocompatibility Antigens Class II/analysis Immunoglobulin D/analysis,immunology,physiology Immunoglobulin Fab Fragments/physiology Immunoglobulin M/immunology,physiology Lymphocyte Activation Mice Mice, Inbred BALB C Mice, Inbred CBA Mice, Inbred DBA Mitogens/physiology Molecular Weight Polymers Serum Albumin, Bovine/immunology,pharmacology
Chemicals
Antibodies, Anti-Idiotypic Antigens, Surface Carrier Proteins Cross-Linking Reagents Dextrans Histocompatibility Antigens Class II Immunoglobulin D Immunoglobulin Fab Fragments Immunoglobulin M Mitogens Polymers anti-IgD anti-IgM Serum Albumin, Bovine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Brunswick M
Department of Medicine, Uniformed Services University, Bethesda, MD 20814.
Finkelman F D
Highet P F
Inman J K
Dintzis H M
Mond J J
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1988-05-15
Pages
3364-72
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
PHS HHS · R01 A121328 · United States
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