| Title | B-cell-tropic interleukins in murine systemic lupus erythematosus (SLE) 1. | | Author(s) | Prud'homme GJ, Fieser TM, Dixon FJ, Theofilopoulos AN | | Source | Immunol Rev 1984 Apr.:159-83. | | MeSH | Animals
Antigens, Differentiation, B-Lymphocyte
Antigens, Surface
B-Lymphocytes
Cell Differentiation
Cell Division
Disease Models, Animal
Female
Growth Substances
Immunoglobulin G
Interleukin-4
Lupus Erythematosus, Systemic
Lymphocyte Activation
Lymphocyte Cooperation
Lymphokines
Macrophages
Male
Mice
Mice, Inbred Strains
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Rodent Diseases
| | Abstract | Functional in vitro studies of B cells from 3 murine strains which develop severe early onset SLE-like disease with marked polyclonal B cell hyperactivity lead to the following conclusions: 1.) B cell proliferation and differentiation in lupus mice remains dependent on accessory signals of either macrophage or T cell origin; 2.) B cells from BXSB, NZB/W and MRL/1 mice appear to require the same number and type of signals as normal B cells to undergo polyclonal or antigen-directed responses. B cells of BXSB and NZB/W, but not MRL/1, origin differ from normal B cells by their higher sensitivity (or degree of response) to the signals they receive; 3.) Proliferating T cells in enlarged nodes and spleens of older MRL/1 mice, in the absence of mitogens, secrete in vitro abnormally high levels of a factor (L-BCDF) inducing terminal differentiation of activated B cells to Ig secreting cells. Based on these findings, murine SLE can be divided into 2 main types which may, nevertheless, share some characteristics: Type 1 murine SLE, characterized by primary B cell hyperresponsiveness to activating signals and lymphokines promoting B cell growth and differentiation (NZ and BXSB strains); and, Type 2 murine SLE, characterized by T helper cell hyperactivity and overproduction by proliferating T cells of one or more B cell differentiation factors (MRL/1 strain). In both types of murine SLE, abnormal responses to accessory signals or overproduction of differentiation-inducing signals ultimately leads to polyclonal and auto-antigen specific B cell expansion, hypergammaglobulinemia and auto-antibody production, and Ig gene rearrangement (IgM to IgG switching), resulting in the production of pathogenic IgG type auto-antibodies and disease. | | Language | eng | | Pub Type(s) | Journal Article
Review
| | PubMed ID | 6429033 |
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