Collagen-induced arthritis in mice. Relationship of collagen-specific and total IgE synthesis to disease

• Published in: The Journal of immunology (1950) Vol. 147; no. 12; pp. 4185 - 4191
• Main Authors: Marcelletti, JF, Ohara, J, Katz, DH
• Format: Journal Article
• Language: English
• Published: United States Am Assoc Immnol 15.12.1991
• Subjects: Animals; Arthritis - etiology; Arthritis - immunology; Autoimmune Diseases - etiology; Cell Degranulation; Collagen - immunology; Immunization; Immunoglobulin E - biosynthesis; Immunoglobulin G - biosynthesis; Interleukin-4 - biosynthesis; Interleukin-4 - pharmacology; Male; Mice; Mice, Inbred BALB C; Mice, Inbred DBA
• DOI: 10.4049/jimmunol.147.12.4185
• ISSN: 0022-1767

The relationship between production of IgE and collagen-induced arthritis in mice was examined. Collagen-specific IgE was produced as a consequence of immunization of DBA/1 mice with chicken type II collagen emulsified in CFA. We observed a rise in collagen-specific IgE antibody levels at the onset of CIA clinical and histologic signs in DBA/1 mice. This rise in IgE paralleled that of IgG2a anticollagen antibodies, an isotype implicated in the pathogenesis of CIA by other laboratories. The collagen-specific IgE contained in the plasma of mice with CIA could arm basophils for Ag- (collagen) dependent degranulation. Collagen-specific IgE may thus contribute to CIA by promoting mast cell degranulation in the synovia of susceptible mice immunized with chick type II collagen; but, further work is required to establish such a role for IgE in CIA. However, genetic differences in disease susceptibility could not be accounted for by quantitative differences in collagen-specific IgE production. Further, comparable levels of IgE anticollagen antibodies were observed in animals with active CIA and after spontaneous remission, thereby confirming that the presence of such antibodies is insufficient for disease. Total IgE levels peaked just before spontaneous remission indicating active production of IL-4. IL-4 was administered to animals with CIA to determine if this lymphokine could be involved in the remission process. IL-4 facilitated remission of CIA. Enhanced total IgE production may thus be a marker for activation of Th2 cells that produce lymphokines such as IL-4 and IL-10, factors that may be involved in the spontaneous remission process.