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PMID: 3493148 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Lymphoma models for B cell activation and tolerance. IV. Growth inhibition by anti-Ig of CH31 and CH33 B lymphoma cells.

European journal of immunology ·Vol. 16 ·No. 12 ·1986-12-00 ·Pages 1577-81

Pennell CA, Scott DW

Abstract

CH31 and CH33 are B cell lymphomas whose growth in vitro is inhibited by anti-Ig reagents, including both polyclonal and monoclonal anti-mu antibodies, and an anti-idiotype antiserum. Antibodies against class I or class II major histocompatibility complex antigens do not affect the growth of these cells. Inhibition is dependent on surface Ig cross-linking and does not require ligand binding to Fc receptors. Interestingly, the inhibition of growth by anti-mu is reversed in CH31 (but not CH33) by E. coli lipopolysaccharide. These lymphomas should provide excellent models to study the mechanisms of growth inhibition mediated by surface Ig cross-linking and the pathways of its reversal.

MeSH Terms
Animals Antibodies, Anti-Idiotypic/immunology B-Lymphocytes/immunology Immune Tolerance Interphase Kinetics Lipopolysaccharides/pharmacology Lymphocyte Activation Lymphoma/immunology,pathology Mice Protein Kinase C/analysis Rabbits Receptors, Antigen, B-Cell/immunology Receptors, Fc/immunology
Chemicals
Antibodies, Anti-Idiotypic Lipopolysaccharides Receptors, Antigen, B-Cell Receptors, Fc Protein Kinase C
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Pennell C A
Scott D W
Article Info
Journal
European journal of immunology
Abbr.
Eur J Immunol
ISSN
0014-2980
Published
1986-12-00
Pages
1577-81
Language
English
Region
Germany
NLM ID
1273201
Subset
IM
Grants
NIAID NIH HHS · AI-20757 · United States
NCI NIH HHS · CA-41363 · United States
NCRR NIH HHS · RR050403 · United States
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