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PMID:8879212

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Citation

Pasparakis, M, Alexopoulou, L, Episkopou, V and Kollias, G (1996) Immune and inflammatory responses in TNF alpha-deficient mice: a critical requirement for TNF alpha in the formation of primary B cell follicles, follicular dendritic cell networks and germinal centers, and in the maturation of the humoral immune response. J. Exp. Med. 184:1397-411

Abstract

To investigate the role of TNF alpha in the development of in vivo immune response we have generated TNF alpha-deficient mice by gene targeting. Homozygous mutant mice are viable and fertile, develop lymph nodes and Peyer's patches and show no apparent phenotypic abnormalities, indicating that TNF alpha is not required for normal mouse development. In the absence of TNF alpha mice readily succumb to L. monocytogenes infections and show reduced contact hypersensitivity responses. Furthermore, TNF alpha knockout mice are resistant to the systemic toxicity of LPS upon D-galactosamine sensitization, yet they remain sensitive to high doses of LPS alone. Most interestingly, TNF alpha knockout mice completely lack splenic primary B cell follicles and cannot form organized follicular dendritic cell (FDC) networks and germinal centers. However, despite the absence of B cell follicles, Ig class-switching can still occur, yet deregulated humoral immune responses against either thymus-dependent (TD) or thymus-independent (TI) antigens are observed. Complementation of TNF alpha functioning by the expression of either human or murine TNF alpha transgenes is sufficient to reconstitute these defects, establishing a physiological role for TNF alpha in regulating the development and organization of splenic follicular architecture and in the maturation of the humoral immune response.

Links

PubMed PMC2192824

Keywords

Animals; Antibody Formation; B-Lymphocytes/immunology; Cell Communication; Dendritic Cells/immunology; Dermatitis, Contact; Female; Germinal Center; Immune System/growth & development; Lipopolysaccharides/toxicity; Listeria monocytogenes/immunology; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Spleen/anatomy & histology; Spleen/immunology; T-Lymphocytes/immunology; Tumor Necrosis Factor-alpha/deficiency; Tumor Necrosis Factor-alpha/genetics

Significance

Annotations

Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status


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References

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