B-cell-tropic interleukins in murine systemic lupus erythematosus (SLE) 1

• Published in: Immunological reviews Vol. 78; p. 159
• Main Authors: Prud'homme, G J, Fieser, T M, Dixon, F J, Theofilopoulos, A N
• Format: Journal Article
• Language: English
• Published: England 01.04.1984
• Subjects: Animals; Antigens, Differentiation, B-Lymphocyte; Antigens, Surface - immunology; B-Lymphocytes - immunology; Cell Differentiation; Cell Division; Disease Models, Animal; Female; Growth Substances - immunology; Immunoglobulin G - immunology; Interleukin-4; Lupus Erythematosus, Systemic - genetics; Lupus Erythematosus, Systemic - immunology; Lupus Erythematosus, Systemic - veterinary; Lymphocyte Activation; Lymphocyte Cooperation; Lymphokines - immunology; Macrophages - immunology; Male; Mice; Mice, Inbred Strains - immunology; Rodent Diseases - genetics; Rodent Diseases - immunology
• ISSN: 0105-2896
• DOI: 10.1111/j.1600-065X.1984.tb00481.x

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.